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1.
Bioorg Chem ; 107: 104516, 2021 02.
Article in English | MEDLINE | ID: mdl-33293057

ABSTRACT

An analog of γ1 laminin (RDIAEIIKDI) decapeptide has been used to augment neuronal survival and regeneration after injuries, during aging and other CNS disorder. As a prime synthetic peptide, KDI, is responsible for the neurite outgrowth of human embryonic neurons. In this study, we have designed, modified a KDI derivative and synthesized by replacing isoleucine (I) with Pro (P) amino acid at C-terminal to enhance its potency towards neurite growth. -Cys-Gly-Cys (-CGC) N2S2 motif was also incorporated in the present design for peptide radiolabeling. The modified peptide showed a better binding with the desired 3T1M receptor for neurite growth. The peptide was synthesized using solid phase peptide synthesis and Fmoc-strategy with more than 80% yield. The receptor binding studies of 99mTc-N2S2-KDP in Neuro2A cell lines showed Kd value in 31 nM range and the complex showed appreciable brain uptake in mice. The results on human SH-SY5Y indicate that the unlabeled N2S2-KDP may perhaps be useful for neurite growth in neurodegenerative disorder.


Subject(s)
Laminin/pharmacology , Neuronal Outgrowth/drug effects , Neurons/drug effects , Radiopharmaceuticals/pharmacology , Animals , Blood Proteins/metabolism , Brain/diagnostic imaging , Cell Line, Tumor , Galectins/metabolism , Humans , Laminin/chemical synthesis , Laminin/metabolism , Laminin/pharmacokinetics , Mice, Nude , Molecular Docking Simulation , Molecular Imaging , Protein Binding , Rabbits , Radiopharmaceuticals/chemical synthesis , Radiopharmaceuticals/metabolism , Radiopharmaceuticals/pharmacokinetics
2.
Exp Eye Res ; 143: 60-7, 2016 Feb.
Article in English | MEDLINE | ID: mdl-26474493

ABSTRACT

Nanofiber-based hydrogels (nanogels) with different, covalently bound peptides were used as an extracellular environment for lens epithelial cells (LECs) in order to modulate the capsular opacification (CO) response after lens surgery in a porcine eye model. Lenses were divided into 15 groups (n = 4 per group), the lens content was removed and the empty capsules were refilled with nanogel without peptides and nanogels with 13 combinations of 5 different peptides: two laminin-derived, two fibronectin-derived, and one collagen IV-derived peptide representing cell adhesion motifs. A control group of 4 lenses was refilled with hyaluronan. After refilling, lenses were extracted from the porcine eye and cultured for three weeks. LECs were assessed for morphology and alpha smooth muscle actin (αSMA) expression using confocal laser scanning microscopy. Compared to hyaluronan controls, lenses filled with nanogel had less CO formation, indicated by a lower αSMA expression (P = 0.004). Microscopy showed differences in morphological cell response within the nanogel refilled groups. αSMA expression in these groups was highest in lenses refilled with nanogel without peptides (9.54 ± 11.29%). Overall, LEC transformation is reduced by the presence of nanogels and the response is improved even further by incorporation of extracellular matrix peptides representing adhesion motifs. Thus, nanomaterials targeting biological pathways, in our case interactions with integrin signaling, are a promising avenue toward reduction of CO. Further research is needed to optimize nanogel-peptide combinations that fully prevent CO.


Subject(s)
Capsule Opacification/prevention & control , Epithelial Cells/cytology , Epithelial-Mesenchymal Transition/drug effects , Extracellular Matrix Proteins/administration & dosage , Hydrogels , Lens Capsule, Crystalline/cytology , Oligopeptides/administration & dosage , Actins/metabolism , Animals , Biomarkers/metabolism , Capsule Opacification/pathology , Collagen Type IV/administration & dosage , Collagen Type IV/chemical synthesis , Drug Delivery Systems , Extracellular Matrix Proteins/chemical synthesis , Fibronectins/administration & dosage , Fibronectins/chemical synthesis , Fluorescent Antibody Technique, Indirect , Laminin/administration & dosage , Laminin/chemical synthesis , Lens, Crystalline/cytology , Nanofibers , Oligopeptides/chemical synthesis , Organ Culture Techniques , Sus scrofa
3.
ACS Appl Mater Interfaces ; 7(4): 2183-8, 2015 Feb 04.
Article in English | MEDLINE | ID: mdl-25585718

ABSTRACT

We report a microfluidic approach to impart alignment in ECM components in 3D hydrogels by continuously applying fluid flow across the bulk gel during the gelation process. The microfluidic device where each channel can be independently filled was tilted at 90° to generate continuous flow across the Matrigel as it gelled. The presence of flow helped that more than 70% of ECM components were oriented along the direction of flow, compared with randomly cross-linked Matrigel. Following the oriented ECM components, primary rat cortical neurons and mouse neural stem cells showed oriented outgrowth of neuronal processes within the 3D Matrigel matrix.


Subject(s)
Cell Culture Techniques/methods , Collagen/chemistry , Extracellular Matrix/metabolism , Laminin/chemistry , Microfluidic Analytical Techniques/methods , Neurons/cytology , Proteoglycans/chemistry , Stem Cells/cytology , Animals , Cell Culture Techniques/instrumentation , Cell Proliferation , Cells, Cultured , Collagen/chemical synthesis , Drug Combinations , Laminin/chemical synthesis , Mice , Microfluidic Analytical Techniques/instrumentation , Neurons/chemistry , Proteoglycans/chemical synthesis , Rats , Stem Cells/chemistry
4.
Biomaterials ; 34(30): 7381-8, 2013 Oct.
Article in English | MEDLINE | ID: mdl-23849345

ABSTRACT

Cell delivery to the pathological intervertebral disc (IVD) has significant therapeutic potential for enhancing IVD regeneration. The development of injectable biomaterials that retain delivered cells, promote cell survival, and maintain or promote an NP cell phenotype in vivo remains a significant challenge. Previous studies have demonstrated NP cell - laminin interactions in the nucleus pulposus (NP) region of the IVD that promote cell attachment and biosynthesis. These findings suggest that incorporating laminin ligands into carriers for cell delivery may be beneficial for promoting NP cell survival and phenotype. Here, an injectable, laminin-111 functionalized poly(ethylene glycol) (PEG-LM111) hydrogel was developed as a biomaterial carrier for cell delivery to the IVD. We evaluated the mechanical properties of the PEG-LM111 hydrogel, and its ability to retain delivered cells in the IVD space. Gelation occurred in approximately 20 min without an initiator, with dynamic shear moduli in the range of 0.9-1.4 kPa. Primary NP cell retention in cultured IVD explants was significantly higher over 14 days when cells were delivered within a PEG-LM111 carrier, as compared to cells in liquid suspension. Together, these results suggest this injectable laminin-functionalized biomaterial may be an easy to use carrier for delivering cells to the IVD.


Subject(s)
Hydrogel, Polyethylene Glycol Dimethacrylate/pharmacology , Intervertebral Disc/physiology , Laminin/pharmacology , Regeneration/drug effects , Animals , Biocompatible Materials/pharmacology , Cells, Cultured , Humans , Hydrogel, Polyethylene Glycol Dimethacrylate/chemical synthesis , Hydrogel, Polyethylene Glycol Dimethacrylate/chemistry , Injections , Intervertebral Disc/cytology , Intervertebral Disc/drug effects , Intervertebral Disc/transplantation , Laminin/chemical synthesis , Laminin/chemistry , Luciferases/metabolism , Mechanical Phenomena/drug effects , Polyethylene Glycols/chemical synthesis , Polyethylene Glycols/chemistry , Polyethylene Glycols/pharmacology , Rats , Rats, Sprague-Dawley , Rheology/drug effects , Sus scrofa
5.
Arq. bras. med. vet. zootec ; 63(1): 28-35, Feb. 2011. ilus
Article in English | LILACS | ID: lil-582320

ABSTRACT

Forty-eight cases of canine mammary cancer were investigated to evaluate the immunohistochemical distribution of the γ2 chain of laminin-332. Tumor cells were compared to a pool of normal mammary tissues using quantitative RT-PCR. The western blot was performed in eight tumor samples as complementary test to evaluate protein integrity. Immunohistochemistry experiments showed negative, focal, and weak expression of laminin-332 γ2 in tumors with the worst prognosis. Quantitative PCR revealed downregulation of the gene in 27 (56.2 percent) of the animals. Out of the 16 dogs with γ2 chain overexpression, seven were still alive. The western blot results showed bands generation of 36, 50, and 98kDa, suggesting degradation of laminin-332 γ2 in malignant tumors. The results suggest that, in the future, low expression and/or degradation of laminin-332 γ2 chain in canine mammary tumors may be used as an indicator of malignant potential. However, further studies are necessary to corroborate these results.


Para avaliar a expressão imunoistoquímica da cadeia γ 2 da laminina-332, foram investigados 48 casos de câncer mamário canino. Comparou-se, por RT-PCR, a expressão gênica nas células tumorais com um pool de tecido mamário. Como teste complementar, em oito amostras tumorais, realizou-se western blot para avaliar a integridade da proteína laminina-332 γ 2. A imunoistoquímica demonstrou expressão negativa, focal e fraca da laminina-332 γ 2 nos tumores com pior prognóstico. A RT-PCR quantitativa revelou a baixa expressão do gene em 27 (56,2 por cento) dos animais. Das 16 cadelas com superexpressão da cadeia γ 2, sete ainda estavam vivas no final do estudo. O resultado do western blot mostrou bandas de 36, 50 e 98kDa, sugerindo uma degradação da laminina-332 γ 2 em tumores malignos. Os resultados sugerem que, no futuro, a baixa expressão e/ou degradação da laminina-332 γ 2 nos tumores mamários caninos podem ser utilizadas como indicadores de potencial maligno. No entanto, mais estudos são necessários para confirmar estes resultados.


Subject(s)
Animals , Dogs/classification , Breast Neoplasms/pathology , Immunohistochemistry , Laminin/chemical synthesis
6.
Arch Biochem Biophys ; 503(2): 213-22, 2010 Nov 15.
Article in English | MEDLINE | ID: mdl-20727343

ABSTRACT

Cell adhesive peptides have been widely applied for therapeutic drugs, drug delivery systems, and biomaterials. Previously, we identified various cell adhesive sequences in the G domains of four laminin α chains (α2-α5) by the systematic soluble peptide screening. We also identified five cell-binding sequences in the laminin α1 chain G domain using synthetic peptide-polystyrene beads. Here, we re-screened cell adhesive peptides in the laminin α1 chain G domain by the systematic soluble peptides screening. The 110 soluble peptides were evaluated for their cell adhesive activities using human fibrosarcoma HT1080 cells and human dermal fibroblasts. Fourteen peptides were newly identified as a cell adhesive. Additionally, four peptides (AG22: SSFHFDGSGYAM, AG42: TFDLLRNSYGVRK, AG76: HQNQMDYATLQLQ, AG86: LGGLPSHYRARNI) promoted integrin-mediated cell adhesion. Further, neurite outgrowth activity with rat pheochromocytoma PC12 cells was evaluated and two peptides (AG20: SIGLWNYIEREGK, AG26: SPNGLLFYLASNG) were newly identified for neurite outgrowth activity. These results suggested that the systematic soluble peptides screening approach is an accurate and powerful strategy for finding biologically active sequences. The active sequences newly identified here could be involved in the biological functions of this domain. The active peptides are useful for evaluating molecular mechanisms of laminin-receptor interactions and for developing cell adhesive biomaterials.


Subject(s)
Laminin/chemistry , Peptides/metabolism , Amino Acid Sequence , Animals , Binding Sites/genetics , Cell Adhesion , Edetic Acid/pharmacology , Heparin/pharmacology , Humans , Integrins/immunology , Integrins/metabolism , Laminin/chemical synthesis , Mice , Molecular Sequence Data , Neurites/metabolism , Phosphorylation , Protein Binding/genetics , Protein Structure, Secondary , Protein Structure, Tertiary/genetics , Rats
7.
J Biomater Sci Polym Ed ; 21(8-9): 1081-101, 2010.
Article in English | MEDLINE | ID: mdl-20507710

ABSTRACT

Schwann cell basal lamina is a nanometer-thin extracellular matrix layer that separates the axon-bound Schwann cells from the endoneurium of the peripheral nerve. It is implicated in the promotion of nerve regeneration after transection injury by allowing Schwann cell colonization and axonal guidance. Hence, it is desired to mimic the native basal lamina for neural tissue engineering applications. In this study, basal lamina proteins from BD Matrigel (growth factor-reduced) were extracted and electrospun to deposit nonwoven nanofiber mats. Adjustment of solute protein concentration, potential difference, air gap distance and flow rate produced a basal lamina-like construct with an average surface roughness of 23 nm and composed of 100-nm-thick irregular and relatively discontinuous fibers. Culture of embryonic chick dorsal root ganglion explants demonstrated that the fabricated nanofiber layer supported explant attachment, elongation of neurites, and migration of satellite Schwann cells in a similar fashion compared to electrospun collagen type-I fibers. Furthermore, the presence of nanorough surface features significantly increased the neurite spreading and Schwann cell growth. Sciatic nerve segment incubation also showed that the construct is promigratory to nerve Schwann cells. Results, therefore, suggest that the synthetic basal lamina fibers can be utilized as a biomaterial for induction of peripheral nerve repair.


Subject(s)
Basement Membrane/chemistry , Biomimetic Materials/chemistry , Collagen/chemistry , Electricity , Laminin/chemistry , Nanofibers/chemistry , Proteoglycans/chemistry , Tissue Engineering/methods , Tissue Scaffolds/chemistry , Animals , Basement Membrane/cytology , Basement Membrane/metabolism , Biomimetic Materials/chemical synthesis , Biomimetic Materials/pharmacology , Cell Enlargement/drug effects , Cell Movement/drug effects , Collagen/chemical synthesis , Collagen/pharmacology , Collagen Type I/chemical synthesis , Collagen Type I/chemistry , Culture Media, Serum-Free , Drug Combinations , Embryo, Nonmammalian , Ganglia, Spinal/cytology , Ganglia, Spinal/drug effects , Ganglia, Spinal/metabolism , Laminin/chemical synthesis , Laminin/pharmacology , Neurites/drug effects , Neurites/metabolism , Polyesters/chemical synthesis , Polyesters/chemistry , Proteoglycans/chemical synthesis , Proteoglycans/pharmacology , Rats , Schwann Cells/cytology , Schwann Cells/drug effects , Sciatic Nerve/cytology , Surface Properties , Trichloroacetic Acid/chemical synthesis , Trichloroacetic Acid/chemistry
8.
Artif Organs ; 32(9): 692-700, 2008 Sep.
Article in English | MEDLINE | ID: mdl-18684206

ABSTRACT

Tissue engineering represents an attractive approach for the treatment of congestive heart failure. The influence of the differentiation of myogenic graft for functional recovery is not defined. We engineered a biodegradable skeletal muscle graft (ESMG) tissue and investigated its functional effect after implantation on the epicardium of an infarcted heart segment. ESMGs were synthesized by mixing collagen (2 mg/mL), Matrigel (2 mg/mL), and rat skeletal muscle cells (10(6)). Qualitative and quantitative aspects of ESMGs were optimized. Two weeks following coronary ligation, the animals were randomized in three groups: ESMG glued to the epicardial surface with fibrin (ESMG, n = 7), fibrin alone (fibrin, n = 5), or sham operation (sham, n = 4). Echocardiography, histology, and immunostaining were performed 4 weeks later. A cohesive three-dimensional tissular structure formed in vitro within 1 week. Myoblasts differentiated into randomly oriented myotubes. Four weeks postimplantation, ESMGs were vascularized and invaded by granulation tissue. Mean fractional shortening (FS) was, however, significantly increased in the ESMG group as compared with preimplantation values (42 +/- 6 vs. 33 +/- 5%, P < 0.05) and reached the values of controlled noninfarcted animals (control, n = 5; 45 +/- 3%; not significant). Pre- and postimplantation FS did not change over these 4 weeks in the sham group and the fibrin-treated animals. This study showed that it is possible to improve systolic heart function following myocardial infarction through implantation of differentiated muscle fibers seeded on a gel-type scaffold despite a low rate of survival.


Subject(s)
Heart/drug effects , Hydrogel, Polyethylene Glycol Dimethacrylate/pharmacology , Muscle, Skeletal/transplantation , Myocardial Infarction/therapy , Animals , Cell- and Tissue-Based Therapy/methods , Collagen/chemical synthesis , Drug Combinations , Female , Heart/physiopathology , Hydrogel, Polyethylene Glycol Dimethacrylate/chemical synthesis , Laminin/chemical synthesis , Muscle Fibers, Skeletal , Muscle, Skeletal/cytology , Muscle, Skeletal/growth & development , Myoblasts, Skeletal/cytology , Myoblasts, Skeletal/transplantation , Myocardial Infarction/diagnostic imaging , Myocardial Infarction/physiopathology , Proteoglycans/chemical synthesis , Random Allocation , Rats , Tissue Culture Techniques/methods , Transplants , Ultrasonography
9.
Langmuir ; 23(23): 11693-704, 2007 Nov 06.
Article in English | MEDLINE | ID: mdl-17918863

ABSTRACT

The influence of lateral ligand mobility on cell attachment and receptor clustering has previously been explored for membrane-anchored molecules involved in cell-cell adhesion. In this study, we considered instead a cell binding motif from the extracellular matrix. Even though the lateral mobility of extracellular matrix ligands in membranes does not occur in vivo, we believe it is of interest for cell engineering in vitro. As is the case for cell-cell adhesion molecules, lateral mobility of extracellular matrix ligands could influence cell attachment and, subsequently, cell behavior in cell culture. In this paper, the accessibility and functionality of extracellular matrix ligands presented at surfaces were evaluated for the conditions of laterally mobile versus non-mobile ligands by studying ligand-antibody binding events and early cell attachment as a function of ligand concentration. We compare the initial attachment of rat-derived adult hippocampal progenitor (AHP) cells on laterally mobile, supported phospholipid bilayer membranes to non-mobile, poly-L-lysine-grafted-poly(ethylene glycol) (PLL-g-PEG) polymer films functionalized with a range of laminin-derived IKVAV-containing peptide densities. To this end, synthesis of a new PLL-g-PEG/PEG-IKVAV polymer is described. The characterization of available IKVAV peptides on both surface presentations schemes was explored by studying the mass uptake of anti-IKVAV antibodies using a combination of the surface-sensitive techniques quartz crystal microbalance with dissipation monitoring, surface plasmon resonance spectroscopy, and optical waveguide lightmode spectroscopy. IKVAV-containing peptides presented on laterally mobile, supported phospholipid bilayers and non-mobile PLL-g-PEG were recognized by the anti-IKVAV antibody in a dose-dependent manner, indicating that the amount of available IKVAV ligands increases proportionally with ligand density over the concentrations tested. Attachment of AHP cells to IKVAV-functionalized PLL-g-PEG and supported phospholipid bilayers followed a sigmoidal dependence on peptide concentration, with a critical concentration of approximately 3 pmol/cm2 IKVAV ligands required to support initial AHP cell attachment for both surface modifications. There appeared to be little influence of IKVAV peptide mobility on the initial attachment of AHP cells. Although the spread in the cell attachment data was larger for the PLL-g-PEG surface modification, this was reduced when observed after 24 h, indicating that the cells might need longer times to establish attachment strengths equivalent to those observed on peptide-functionalized supported lipid bilayers. The present study is a step toward understanding the influence of extracellular-matrix-derived ligand mobility on cell fate. Further analysis should focus on the systematic tuning of lateral ligand diffusion, as well as a comparison between the response of non-spreading cells (i.e., AHPs), versus spreading cells (i.e., fibroblasts).


Subject(s)
Antibody Affinity , Biocompatible Materials/chemical synthesis , Cell Adhesion/physiology , Laminin/chemical synthesis , Peptide Fragments/chemical synthesis , Polyethylene Glycols/chemical synthesis , Polylysine/analogs & derivatives , Amino Acid Sequence , Animals , Antibodies/chemistry , Cells, Cultured , Extracellular Matrix/chemistry , Extracellular Matrix/metabolism , Hippocampus/cytology , Ligands , Molecular Sequence Data , Polylysine/chemical synthesis , Rats
10.
J Colloid Interface Sci ; 263(2): 432-40, 2003 Jul 15.
Article in English | MEDLINE | ID: mdl-12909032

ABSTRACT

The synthesis, physicochemical characterization, and interaction with membrane model systems of a peptide derived from the PA22-2 region of laminin are described. Surface activity studies indicate that this peptide is able to spread at the air-water interface being the maximal spreading pressure 20 mN/m at subphase concentrations around 10 micro M. Besides, these peptide molecules are also able to form stable monolayers. Physicochemical studies concerning the interaction of this peptide with lipids, organized in mono and bilayers, were carried out using Langmuir balance experiments and polarization fluorescence techniques. The peptide penetrates better in monolayers of DPPC than in those of PC and forms condensed mixed monolayers with DPPC. Energies of mixing are small thus indicating that deviations from ideality were almost negligible. Interactions with bilayers were studied through microviscosity changes (DPH and TMA-DPH probes), membrane permeability alterations (CF, NBD-PE/dithionite), and fusion promotion (NBD-PE/Rh-PE, resonance energy transfer). Results indicate that this sequence interacts very softly with bilayers without promoting changes in their organization. These data as well as the lack of interaction with erythrocytes suggest that coating liposomes with this peptide through chemical amide bonds can render stable inmunoliposomes for further biological applications.


Subject(s)
Laminin/chemical synthesis , Laminin/physiology , 1,2-Dipalmitoylphosphatidylcholine/chemistry , Air , Animals , Biophysical Phenomena , Biophysics , Chromatography, High Pressure Liquid , Dose-Response Relationship, Drug , Erythrocytes/metabolism , Fluorescence Resonance Energy Transfer , Kinetics , Laminin/chemistry , Lipid Bilayers/chemistry , Lipids/chemistry , Liposomes/chemistry , Liposomes/metabolism , Models, Statistical , Peptide Biosynthesis , Peptides/chemistry , Pressure , Rabbits , Temperature , Time Factors , Water/chemistry
11.
J Neurosci Res ; 72(5): 646-59, 2003 Jun 01.
Article in English | MEDLINE | ID: mdl-12749030

ABSTRACT

We have developed tendon chitosan tubes having the ability to bind peptides covalently, and the effectiveness of laminin peptides coupled to these tubular wall on nerve regeneration was examined in vivo. Bridge graft implantation (15 mm) into the sciatic nerve of SD rats was carried out using chitosan tubes having a triangular cross section containing either covalently bound intact laminin or the laminin peptides CDPGYIGSR or CSRARKQAASIKVAVSAD or being nontreated (N = 20 in each group). As a control, isografting (N = 5) was carried out. Three rats in each experimental group were sacrificed for histology observations after 1, 2, 4, 6, and 8 weeks. The total area of regenerating tissue in the tube and the length of the area where regenerating tissue attached to the inner surface of the tube were measured. In five rats from each experimental and control group, the latency quotient between the implanted and the nontreated site was determined 12 weeks after implantation. Furthermore, the percentage of myelinated axon area was measured at a 10-mm distance from the distal anastomosed site. Histological findings suggest that the immobilized laminin, confirmed by immunostaining as long as 12 weeks postoperatively, as well as laminin oligopeptides may effectively assist nerve tissue extension. According to statistical analysis of the percentage neural tissue found in relation to evoked action potentials, the sequential treatments with YIGSR first followed by IKVAV matched the effectiveness of intact laminin in enhancing nerve regeneration. However, when compared with that after isografting, the enhancement of regenerated axon growth was less sufficient.


Subject(s)
Absorbable Implants/standards , Chitin/analogs & derivatives , Chitin/pharmacology , Laminin/pharmacology , Nerve Regeneration/drug effects , Sciatic Nerve/surgery , Sciatic Neuropathy/surgery , Absorbable Implants/trends , Action Potentials/drug effects , Action Potentials/physiology , Animals , Axons/drug effects , Axons/metabolism , Axons/ultrastructure , Brachyura , Chitin/therapeutic use , Chitosan , Laminin/chemical synthesis , Laminin/therapeutic use , Male , Microscopy, Electron , Myelin Sheath/drug effects , Myelin Sheath/metabolism , Myelin Sheath/ultrastructure , Nerve Regeneration/physiology , Peptides/chemical synthesis , Peptides/pharmacology , Peptides/therapeutic use , Rats , Rats, Sprague-Dawley , Recovery of Function/drug effects , Recovery of Function/physiology , Schwann Cells/drug effects , Schwann Cells/metabolism , Schwann Cells/ultrastructure , Sciatic Nerve/drug effects , Sciatic Nerve/ultrastructure , Sciatic Neuropathy/drug therapy , Tendons/chemistry , Tendons/transplantation , Treatment Outcome
12.
Exp Cell Res ; 277(1): 95-106, 2002 Jul 01.
Article in English | MEDLINE | ID: mdl-12061820

ABSTRACT

The laminins consist of at least 11 polypeptides (5 alpha-chains, 3 beta-chains, and 3 gamma-chains) specific to basement membranes. Here we investigate the biological activity associated with the G domain of the newly identified laminin alpha5-chain using 113 overlapping synthetic peptides (positions 2679-3635). Using HT-1080 cells, 21 peptides showed attachment activity either on peptide-coated tissue culture plates or to peptide-conjugated Sepharose beads. Heparin inhibited cell attachment to 16 peptides, while ethylenediaminetetraacetic acid exhibited no inhibitory activity. Peptides A5G-27, A5G-65, and A5G-71 showed the strongest cell attachment, with the minimum active core sequences of the peptides being GIIFFL, HQNMGSVNVSV, and YLQFVG, respectively. Furthermore, these 16 peptides were tested for their ability to stimulate neurite outgrowth in the PC12 cells. A5G-3, A5G-33, A5G-71, A5G-73, A5G-81, and A5G-101 were the only peptides of the 16 that demonstrated the ability to promote neurite outgrowth. These results demonstrate that synthetic peptides with alpha5-chain G domain primary amino acid sequences possess some of the same biological activities attributable to the whole laminin and the alpha5-chain G domain. Therefore, these peptides may be useful in the investigation of laminin-receptor interactions and possibly mechanisms of laminin signal transduction.


Subject(s)
Laminin/metabolism , Peptides/metabolism , Amino Acid Sequence , Animals , Binding Sites , Cell Division/drug effects , Humans , Laminin/chemical synthesis , Molecular Sequence Data , Neurites/drug effects , Neurites/physiology , PC12 Cells , Peptides/chemical synthesis , Plastics , Protein Structure, Tertiary , Rats , Recombinant Fusion Proteins/metabolism , Sepharose , Tumor Cells, Cultured
13.
Chem Pharm Bull (Tokyo) ; 49(4): 488-91, 2001 Apr.
Article in English | MEDLINE | ID: mdl-11310682

ABSTRACT

Poly(ethylene glycol) (PEG) has been studied as a drug-carrier for proteins, but not for small peptides. Laminin, a cell adhesive protein, has Tyr-Ile-Gly-Ser-Arg (YIGSR) sequence and peptides containing this sequence inhibit experimental metastasis. We have studied PEG hybrids of YIGSR and other small laminin-related peptides. In a previous paper, we reported preparation of YIGSR-PEG hybrids by combination of the solid phase method and the solution method, but the synthetic procedure was problematic. Here we report a facile synthesis of PEG hybrids of YIGSR (PEG-YIGSR, YIGSR-PEG, PEG-YIGSR-PEG) by the solid phase method.


Subject(s)
Antineoplastic Agents/chemical synthesis , Laminin/chemical synthesis , Peptides/chemical synthesis , Polyethylene Glycols/chemistry , Animals , Antineoplastic Agents/pharmacology , Drug Carriers/chemistry , Laminin/pharmacology , Melanoma, Experimental/drug therapy , Mice , Mice, Inbred C57BL , Neoplasm Metastasis/pathology , Neoplasm Metastasis/prevention & control , Peptides/pharmacology , Tumor Cells, Cultured
14.
Biochim Biophys Acta ; 1481(1): 25-36, 2000 Aug 31.
Article in English | MEDLINE | ID: mdl-10962089

ABSTRACT

An antagonist of cellular adhesion and motility, acetyl-C-[S-Acm]-VIGYSGDRC-[S-Acm]-NH(2) (mEGF(33-42)), shares homology with the agonist sequence CDPGYIGSR-NH(2). It has been proposed that the latter peptide binds to the high affinity 67 kDa laminin receptor. Both peptides have equal affinities for the receptor and similar conformations have been derived for both. We have examined the importance of individual non-homologous residues with respect to receptor binding and antagonistic properties of mEGF(33-42). Alanine scanning of non-conserved residues in the N-terminal half of mEGF(33-42) caused loss of biological activity with respect to cell attachment, receptor binding and migratory response. Substitution of alanine for serine (position 6) caused loss of laminin-specific cell attachment and receptor binding activities. However, the peptide did stimulate migration suggesting that this peptide may be a non-specific stimulator of migration. In contrast, alanine substitution for the C-terminal Cys-S-Acm had no apparent effect on the attachment or receptor binding activities of the peptide but generated an agonist from the antagonist parent. Comparison of the modelled folds of the alanine containing peptides revealed the presence of significant helical content in those peptides capable of stimulating migration and suggests that a reduction in bulk in the N-terminal residues is not conducive to adopting a productive binding conformation.


Subject(s)
Alanine/analysis , Peptides/chemical synthesis , Receptors, Laminin/agonists , Amino Acid Sequence , Animals , Drug Design , Epidermal Growth Factor/chemistry , Laminin/chemical synthesis , Mice , Models, Molecular , Molecular Weight , Protein Binding , Protein Conformation , Protein Isoforms/chemical synthesis , Receptors, Laminin/chemistry , Structure-Activity Relationship
15.
J Biomater Sci Polym Ed ; 10(9): 931-55, 1999.
Article in English | MEDLINE | ID: mdl-10574609

ABSTRACT

In this study, we synthesized a biomaterial whose surface inhibits non-specific protein and cell attachment. The polymer was designed to mimic the external cell plasma membrane properties through the introduction of particular chemical constituents of the cell membrane: phospholipid polar headgroups. This was done by copolymerizing phosphorylcholine (PC) groups into a polyurethane polymer backbone (PCPUR). Peptides known to induce specific cell attachment were subsequently bound to the surface of this copolymer in a photoadressible manner to obtain surfaces that allowed the attachment of cells in a specific pattern. Two polymers with different phosphorylcholine concentrations were synthesized and their bulk and surface properties were characterized through differential scanning calorimetry, wettability measurements, angle-resolved X-ray photoelectron spectroscopy and time-of-flight secondary ion mass spectrometry. Protein and lipid adsorption investigation using optical waveguide light mode spectroscopy showed that the irreversible adsorption of both proteins and lipids is drastically reduced as a result of simultaneous contributions of the PC groups, molecular mobility and strong hydrophilicity of the polymers. Consequently, this leads to a marked reduction in the cellular attachment response, which further decreases with increasing PC concentration. Finally, when the polymer surface was photo-derivatized, attachment of the neural NG108-15 cell line occurred only on the areas of the PCPUR where the laminin CDPGYIGSR peptide sequence was photoimmobilized. Cell attachment was nevertheless found to be non-specific with respect to the peptide sequence used and reasons for such results are therefore discussed.


Subject(s)
Biocompatible Materials/chemistry , Biocompatible Materials/chemical synthesis , Cell Adhesion , Polyurethanes/chemistry , Polyurethanes/chemical synthesis , Proteins/metabolism , Adsorption , Amino Acid Sequence , Animals , Cattle , Cell Line , Humans , In Vitro Techniques , Laminin/chemical synthesis , Laminin/chemistry , Lipid Metabolism , Materials Testing , Mice , Oligopeptides/chemical synthesis , Oligopeptides/chemistry , Phosphorylcholine/chemical synthesis , Phosphorylcholine/chemistry , Rats , Surface Properties
16.
FASEB J ; 13(1): 53-62, 1999 Jan.
Article in English | MEDLINE | ID: mdl-9872929

ABSTRACT

Laminin-1 is a basement membrane glycoprotein that promotes several biological activities including cell attachment, tumor metastasis, and angiogenesis. Angiogenesis plays an important role in tissue formation, reproduction, wound healing, and several pathological conditions. In this study, we screened 405 synthetic peptides from the alpha1 and beta1 chains to identify potential sites on laminin-1 active with endothelial cells. Peptides were initially screened by testing both endothelial cell adhesion to peptide-coated wells and tube formation on Matrigel in the presence of soluble peptide. Twenty active peptides were identified in these screens. A secondary screen using the rat aortic ring sprouting assay identified 13 of the 20 peptides that stimulated endothelial sprouting. Several of these active peptides were also found to stimulate human umbilical vein endothelial cell migration in Boyden chamber assays. Differences in the amount of peptide needed for the response and in the resultant morphologies/responses were observed between the peptides in all of the assays. Our results suggest that several active domains on laminin-1 may play important roles in stimulating different steps in angiogenesis.


Subject(s)
Cell Adhesion , Endothelium, Vascular/cytology , Laminin/physiology , Neovascularization, Physiologic/physiology , Amino Acid Sequence , Animals , Aorta/physiology , Cell Movement , Cells, Cultured , Humans , Laminin/chemical synthesis , Molecular Sequence Data , Peptides/chemical synthesis , Peptides/metabolism , Rats , Structure-Activity Relationship
17.
J Cell Sci ; 111 ( Pt 14): 1929-40, 1998 Jul 30.
Article in English | MEDLINE | ID: mdl-9645941

ABSTRACT

To study the mechanism of basement membrane formation, we determined by immunochemistry temporal and spatial expression of laminin-5 (Ln-5), laminin-1 (Ln-1) and their integrin receptors during early skin morphogenesis. A 3-dimensional skin culture was used that allows the study of the sequential molecular events of basement membrane formation at the epidermodermal interface. During early anchorage of keratinocytes to the extracellular matrix there is expression of Ln-5, BP-230 antigen and alpha3, beta1 integrin subunits. During epidermal stratification and prior to the formation of the lamina densa there is assembly of Ln-5, Ln-1, collagen IV and nidogen accompanied by keratinocyte basal clustering of alpha2, alpha3, alpha6, beta1, and beta4+ integrin subunits. The assembly pattern of Ln-1 and Ln-5 can be disturbed with functional antibodies against the beta1 (AIIB2) and alpha6 (GoH3) integrin subunits. Ln-1 assembly can also be disturbed with antibodies against its E8 domain and by competitive inhibition with a synthetic peptide (AG-73) derived from its G-4 domain. Quantitative RT-PCR showed that the dermis contributes about 80% of the laminin gamma)1 chain mRNA while 20% is produced by the epidermis which emphasizes its dual tissue origin and the major contribution of the mesenchyma in laminin production. The laminin gamma2 chain mRNA, present in Ln-5, was mostly of epidermal origin. This study presents evidence that during the initiation of basement membrane formation, laminins bind to keratinocyte plasma membrane receptors and thus may serve as nucleation sites for further polymerization of these compounds by a self-assembly process.


Subject(s)
Basement Membrane/physiology , Epidermis/physiology , Keratinocytes/physiology , Laminin/biosynthesis , Skin/cytology , Actin Cytoskeleton/physiology , Actin Cytoskeleton/ultrastructure , Amino Acid Sequence , Basement Membrane/cytology , Cell Communication , Cell Membrane/physiology , Cells, Cultured , Desmosomes/physiology , Desmosomes/ultrastructure , Epidermal Cells , Fibroblasts/cytology , Fibroblasts/physiology , Humans , Immunohistochemistry , Integrin beta1/biosynthesis , Keratinocytes/cytology , Laminin/chemical synthesis , Laminin/metabolism , Male , Morphogenesis , Peptide Fragments/chemical synthesis , Peptide Fragments/metabolism , Skin Physiological Phenomena
18.
Dev Dyn ; 212(3): 394-402, 1998 Jul.
Article in English | MEDLINE | ID: mdl-9671943

ABSTRACT

Active sequences from the laminin alpha1 and alpha2 chain carboxyl-terminal globular domains (G domain) have been identified by screening overlapping synthetic peptides in a number of biological assays (Nomizu et al. [1995] J. Biol. Chem. 270:20583-20590; Nomizu et al. [1996] FEBS Lett. 396:37-42). We have tested the activity of these peptides in submandibular gland explants of embryonic day 13 mice to determine the functional sites involved in organ development. The laminin alpha1 chain peptide, RKRLQVQLSIRT (residues 2719-2730 and designated AG-73), significantly inhibited epithelial branching morphogenesis. In contrast, other cell adhesive laminin alpha1 chain peptides including the AASIKVAVSADR and NRWHSIYITRFG failed to inhibit the branching. MG-73, a homologue of AG-73 from the laminin alpha2 chain, did not inhibit the branching. The alpha2 chain peptide had no effect, which may be due to the low levels of this laminin chain in day 13 mice. Laminin alpha2 chain-specific monoclonal antibodies strongly reacted with the basement membranes of developed acini but only weakly stained embryonic day 13 submandibular epithelium. The expression of E-cadherin and alpha6 integrin, as detected by immunofluorescence, were unchanged in both AG-73 and control scramble peptide-treated epithelial cells of the explants. In contrast, immunostaining of nidogen/entactin showed that explants treated with AG-73 for 3 days had a discontinuous basement membrane. Explants treated for 3 days with control peptide showed a normal basement membrane. These results suggest that the region containing the AG-73 sequence of the laminin alpha1 chain is crucial for development of submandibular gland at early embryonic stages. The discontinuous basement membrane in AG-73-treated explants may indicate an important role for this region in basement membrane assembly.


Subject(s)
Laminin/metabolism , Submandibular Gland/embryology , Submandibular Gland/metabolism , Animals , Basement Membrane , Culture Techniques , Epithelium/metabolism , Laminin/chemical synthesis , Laminin/pharmacology , Mice , Morphogenesis , Peptides/chemical synthesis , Peptides/pharmacology , Submandibular Gland/drug effects , Submandibular Gland/ultrastructure
19.
J Biomed Mater Res ; 41(2): 278-88, 1998 Aug.
Article in English | MEDLINE | ID: mdl-9638533

ABSTRACT

Interactions between cultured nerve cells and surfaces are of importance for the implantation of biocompatible electrode materials such as glassy carbon (GC). Since implants serve as recording sensors in prosthetic neuroscience, we investigated whether coating electrodes with certain laminin derivatives containing the peptide sequences SIKVAV, CDPGYIGSR, PDSGR, YFQRYLI, and RNIAEIIKDA influences neuronal adhesion and neurite outgrowth in vitro. The coating of GC was performed by electrochemical polymerization and, for comparison, by adsorption or covalent coupling. Electrochemical polymerization is suitable for the coupling of peptides to GC, as shown by amino acid analysis and sequencing. Embryonic chicken retinal ganglion cells and brain cells (days E7 or E17) were used for both attachment and growth studies. Surfaces made by electrochemical polymerization of peptides were more efficient than those made by adsorption or covalent coupling of peptides. Synthetic cyclic peptide derivatives of CDPGYIGSR and 18-mer SIKVAV were found to be more efficient than the linear peptides. Competitive effects that resulted in a decreased cell attachment could be found upon application of soluble peptides. Nevertheless, irrespective of the method of coating, peptides were less efficient compared with the whole laminin molecule, as expected from its multiple adhesion sites. When small GC pins were implanted into the brain of E17 chicken after coating with the 18-mer SIKVAV peptide, nerve cell attachment was observed in vivo. The results suggest that chronically implantable materials may exert a higher neurocompatibility when coated with synthetic peptides.


Subject(s)
Biocompatible Materials/chemistry , Brain/cytology , Carbon/chemistry , Laminin/pharmacology , Neurites/physiology , Peptide Fragments/pharmacology , Peptides, Cyclic/pharmacology , Prostheses and Implants , Retinal Ganglion Cells/cytology , Amino Acid Sequence , Animals , Biocompatible Materials/pharmacology , Brain/embryology , Carbon/pharmacology , Cell Adhesion/drug effects , Cell Division/drug effects , Chick Embryo , Laminin/chemical synthesis , Materials Testing , Molecular Sequence Data , Peptide Fragments/chemical synthesis , Peptides, Cyclic/chemical synthesis , Structure-Activity Relationship , Surface Properties
20.
Chem Pharm Bull (Tokyo) ; 46(2): 347-50, 1998 Feb.
Article in English | MEDLINE | ID: mdl-9501469

ABSTRACT

Analogs of a partial sequence peptide of laminin, i.e., Tyr-Ile-Gly-Ser-Arg (YIGSR) analogs and Cys-Asp-Pro-Gly-Tyr-Ile-Gly-Ser-Arg (CDPGYIGSR) analogs, were prepared by the solid-phase method and their inhibitory effects on experimental metastasis of B16-BL6 melanoma cells were examined. YIGSR analogs in which Ile was replaced by other hydrophobic amino acids (Met, Leu, Phe) were inhibitory. Cys-containing analogs of YIGSR were also prepared, but were less active than the parent peptide, YIGSR. Among them, CYIGSR was easily oxidized to form a disulfide bond. A Cys-containing YIGSR analog cyclized through a disulfide bond, cyclo(CYIGSRC)G, was prepared. The disulfide bond formation was performed on the resin by the silyl chloride-sulfoxide method and by the iodine oxidation method. The yield of the silyl chloride-sulfoxide method was much better than that of the iodine oxidation method.


Subject(s)
Antineoplastic Agents/adverse effects , Antineoplastic Agents/therapeutic use , Laminin/chemical synthesis , Laminin/therapeutic use , Lung Neoplasms/prevention & control , Lung Neoplasms/secondary , Melanoma, Experimental/prevention & control , Melanoma, Experimental/secondary , Oligopeptides/chemical synthesis , Oligopeptides/therapeutic use , Animals , Melanoma, Experimental/drug therapy , Mice , Mice, Inbred C57BL , Neoplasm Transplantation
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