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1.
J Dent Res ; 103(7): 755-764, 2024 Jul.
Article in English | MEDLINE | ID: mdl-38715201

ABSTRACT

Although mesenchyme is essential for inducing the epithelium of ectodermal organs, its precise role in organ-specific epithelial fate determination remains poorly understood. To elucidate the roles of tissue interactions in cellular differentiation, we performed single-cell RNA sequencing and imaging analyses on recombined tissues, where mesenchyme and epithelium were switched ex vivo between two types of embryonic mouse salivary glands: the parotid gland (a serous gland) and the submandibular gland (a predominantly mucous gland). We found partial induction of molecules that define gland-specific acinar and myoepithelial cells in recombined salivary epithelium. The parotid epithelium recombined with submandibular mesenchyme began to express mucous acinar genes not intrinsic to the parotid gland. While myoepithelial cells do not normally line parotid acini, newly induced myoepithelial cells densely populated recombined parotid acini. However, mucous acinar and myoepithelial markers continued to be expressed in submandibular epithelial cells recombined with parotid mesenchyme. Consequently, some epithelial cells appeared to be plastic, such that their fate could still be modified in response to mesenchymal signaling, whereas other epithelial cells appeared to be already committed to a specific fate. We also discovered evidence for bidirectional induction: transcriptional changes were observed not only in the epithelium but also in the mesenchyme after heterotypic tissue recombination. For example, parotid epithelium induced the expression of muscle-related genes in submandibular fibroblasts that began to mimic parotid fibroblast gene expression. These studies provide the first comprehensive unbiased molecular characterization of tissue recombination approaches exploring the regulation of cell fate.


Subject(s)
Cell Differentiation , Mesoderm , Submandibular Gland , Animals , Mice , Submandibular Gland/embryology , Submandibular Gland/cytology , Mesoderm/cytology , Mesoderm/embryology , Parotid Gland/cytology , Parotid Gland/embryology , Parotid Gland/metabolism , Epithelial Cells , Salivary Glands/embryology , Salivary Glands/cytology , Cell Lineage , Acinar Cells , Epithelium/embryology
2.
J Dent Res ; 101(13): 1645-1653, 2022 12.
Article in English | MEDLINE | ID: mdl-36408969

ABSTRACT

Mitigation of irradiation injury to salivary glands was previously reported using a cell-free extract from mouse bone marrow. However, to bring this potential therapy a step closer to clinical application, a human bone marrow cell extract (BMCE) needs to be tested. Here, we report that irradiation-induced injury of salivary glands in immunocompetent mice treated with human BMCE secreted 50% more saliva than saline-injected mice, and BMCE did not cause additional acute inflammatory reaction. In addition, to identify the cell fraction in BMCE with the most therapeutic activity, we sorted human bone marrow into 3 cell fractions (mononuclear, granulocyte, and red blood cells) and tested their respective cell extracts. We identified that the mononuclear cell extract (MCE) provided the best therapeutic efficacy. It increased salivary flow 50% to 73% for 16 wk, preserved salivary parenchymal and stromal cells, and doubled cell proliferation rates while producing less inflammatory response. In contrast, the cell extract of granulocytes was of shorter efficacy and induced an acute inflammatory response, while that from red blood cells was not therapeutically effective for salivary function. Several proangiogenic (MMP-8, MMP-9, VEGF, uPA) and antiangiogenic factors (TSP-1, PF4, TIMP-1, PAI-1) were identified in MCE. Added advantages of BMCE and MCE for potential clinical use were that cell extracts from both male and female donors were comparably bioactive and that cell extracts could be stored and transported much more conveniently than cells. These findings suggest human BMCE, specifically the MCE fraction, is a promising therapy against irradiation-induced salivary hypofunction.


Subject(s)
Radiation Injuries , Salivary Glands , Humans , Male , Female , Mice , Animals , Cell Extracts/pharmacology , Salivary Glands/radiation effects , Bone Marrow Cells , Saliva
3.
J Dent Res ; 101(5): 495-504, 2022 05.
Article in English | MEDLINE | ID: mdl-34875908

ABSTRACT

The extracellular matrix (ECM) is a highly dynamic amalgamation of structural and signaling molecules whose quantitative and qualitative modifications drive the distinct programmed morphologic changes required for tissues to mature into their functional forms. The craniofacial complex houses a diverse array of tissues, including sensory organs, glands, and components of the musculoskeletal, neural, and vascular systems, alongside several other highly specialized tissues to form the most complex part of the vertebrate body. Through cell-ECM interactions, the ECM coordinates the cell movements, shape changes, differentiation, gene expression changes, and other behaviors that sculpt developing organs. In this review, we focus on several common key roles of the ECM to shape developing craniofacial organs and tissues. We summarize recent advances in our understanding of the ability of the ECM to biochemically and biomechanically orchestrate major events of craniofacial development, and we discuss how dysregulated ECM dynamics contributes to disease and disorders. As we expand our understanding of organ-specific matrix functionality and composition, we will improve our ability to rationally modify matrices to promote regeneration and/or prevent degenerative outcomes in vitro and in vivo.


Subject(s)
Extracellular Matrix , Cell Differentiation , Cell Movement , Extracellular Matrix/metabolism , Humans
4.
J Dent Res ; 99(1): 69-78, 2020 01.
Article in English | MEDLINE | ID: mdl-31644367

ABSTRACT

Branching organs, including the salivary and mammary glands, lung, and kidney, arise as epithelial buds that are morphologically very similar. However, the mesenchyme is known to guide epithelial morphogenesis and to help govern cell fate and eventual organ specificity. We performed single-cell transcriptome analyses of 14,441 cells from embryonic day 12 submandibular and parotid salivary glands to characterize their molecular identities during bud initiation. The mesenchymal cells were considerably more heterogeneous by clustering analysis than the epithelial cells. Nonetheless, distinct clusters were evident among even the epithelial cells, where unique molecular markers separated presumptive bud and duct cells. Mesenchymal cells formed separate, well-defined clusters specific to each gland. Neuronal and muscle cells of the 2 glands in particular showed different markers and localization patterns. Several gland-specific genes were characteristic of different rhombomeres. A muscle cluster was prominent in the parotid, which was not myoepithelial or vascular smooth muscle. Instead, the muscle cluster expressed genes that mediate skeletal muscle differentiation and function. Striated muscle was indeed found later in development surrounding the parotid gland. Distinct spatial localization patterns of neuronal and muscle cells in embryonic stages appear to foreshadow later differences in adult organ function. These findings demonstrate that the establishment of transcriptional identities emerges early in development, primarily in the mesenchyme of developing salivary glands. We present the first comprehensive description of molecular signatures that define specific cellular landmarks for the bud initiation stage, when the neural crest-derived ectomesenchyme predominates in the salivary mesenchyme that immediately surrounds the budding epithelium. We also provide the first transcriptome data for the largely understudied embryonic parotid gland as compared with the submandibular gland, focusing on the mesenchymal cell populations.


Subject(s)
Salivary Glands , Submandibular Gland , Animals , Epithelial Cells , Mice , Mice, Inbred ICR , Morphogenesis , Salivary Glands/cytology , Salivary Glands/embryology , Sequence Analysis, RNA
5.
J Dent Res ; 95(13): 1518-1527, 2016 Dec.
Article in English | MEDLINE | ID: mdl-27542391

ABSTRACT

Cells engage in bidirectional communication with their surroundings. This reciprocal dialogue between cells and their cellular microenvironments often governs the maintenance and differentiation of stem/progenitor cells. Here, the authors present evidence that in developing salivary gland explants, a single posttranslational change in microtubules in mesenchymal cells alters the mesenchymal microenvironment and promotes the maintenance and differentiation of a subset of epithelial progenitor cells that impairs branching morphogenesis. Specifically, the authors report that hyperacetylation of microtubules in mesenchymal cells increased cytokeratin 14-positive (K14+) progenitors and their differentiated progeny, myoepithelial cells, in epithelial basal and suprabasal layers in the distal endbud region of developing salivary glands. Mechanistically, this process engages the transforming growth factor ß1 protein and Notch signaling pathways. This report establishes that a simple posttranslational change in the cytoskeletal system of mesenchyme dictates the maintenance and differentiation of adjacent epithelial progenitor cells to alter branching morphogenesis of the epithelium.


Subject(s)
Keratin-14/metabolism , Mesenchymal Stem Cells/metabolism , Microtubules/metabolism , Salivary Glands/embryology , Acetylation , Animals , Cell Communication , Cell Differentiation , Extracellular Matrix/metabolism , Fibronectins/pharmacology , Manganese/pharmacology , Mice , Organ Culture Techniques , Receptors, Notch/metabolism , Signal Transduction , Transforming Growth Factor beta/metabolism
6.
J Dent Res ; 91(2): 197-202, 2012 Feb.
Article in English | MEDLINE | ID: mdl-22095070

ABSTRACT

Branching morphogenesis is essential for the formation of salivary glands, kidneys, lungs, and many other organs during development, but the mechanisms underlying this process are not adequately understood. Microarray and other gene expression methods have been powerful approaches for identifying candidate genes that potentially regulate branching morphogenesis. However, functional validation of the proposed roles for these genes has been severely hampered by the absence of efficient techniques to genetically manipulate cells within embryonic organs. Using ex vivo cultured embryonic mouse submandibular glands (SMGs) as models to study branching morphogenesis, we have identified new vectors for viral gene transfer with high efficiency and cell-type specificity to developing SMGs. We screened adenovirus, lentivirus, and 11 types of adeno-associated viruses (AAV) for their ability to transduce embryonic day 12 or 13 SMGs. We identified two AAV types, AAV2 and bovine AAV (BAAV), that are selective in targeting expression differentially to SMG epithelial and mesenchymal cell populations, respectively. Transduction of SMG epithelia with self-complementary (sc) AAV2 expressing fibroblast growth factor 7 (Fgf7) supported gland survival and enhanced SMG branching morphogenesis. Our findings represent, to our knowledge, the first successful selective gene targeting to epithelial vs. mesenchymal cells in an organ undergoing branching morphogenesis.


Subject(s)
Genes, Viral/genetics , Salivary Glands/embryology , Adenoviridae/genetics , Animals , Cattle , Cell Culture Techniques , Cell Line , Dependovirus/genetics , Epithelial Cells/physiology , Feasibility Studies , Fibroblast Growth Factor 7/genetics , Gene Expression Regulation, Developmental/genetics , Gene Transfer Techniques , Genes, Reporter/genetics , Genetic Vectors/genetics , Green Fluorescent Proteins/genetics , HEK293 Cells , Humans , Lentivirus/genetics , Luminescent Agents , Mesoderm/cytology , Mice , Morphogenesis/genetics , Organ Culture Techniques , Plasmids/genetics , Tissue Survival/genetics , Transduction, Genetic/methods , Transfection
7.
J Dent Res ; 90(9): 1078-84, 2011 Sep.
Article in English | MEDLINE | ID: mdl-21709141

ABSTRACT

During organ development, local changes in gene expression govern morphogenesis and cell fate. We have generated a microanatomical atlas of epithelial gene expression of embryonic salivary glands. The mouse submandibular salivary gland first appears as a single mass of epithelial cells surrounded by mesenchyme, and it undergoes rapid branching morphogenesis to form a complex secretory organ with acini connected to an extensive ductal system. Using laser capture microdissection, we collected samples from 14 distinct epithelial locations at embryonic days 12.5, 13.5, 14, and 15, and characterized their gene expression by microarray analysis. These microarray results were evaluated by qPCR of biological replicates and by comparisons of the gene expression dataset with published expression data. Using this gene expression atlas to search for novel regulators of branching morphogenesis, we found a substantial reduction in mRNA levels of GSK3ß at the base of forming clefts. This unexpected finding was confirmed by immunostaining, and inhibition of GSK3ß activity enhanced salivary gland branching. This first microanatomical expression atlas of a developing gland characterizes changes in local gene expression during salivary gland development and differentiation, which should facilitate the identification of key genes involved in tissue morphogenesis.


Subject(s)
Databases, Genetic , Gene Expression Regulation, Developmental , Glycogen Synthase Kinase 3/physiology , Organogenesis/genetics , Submandibular Gland/embryology , Animals , Chromosome Mapping , Down-Regulation , Epithelial Cells/physiology , Gene Expression Profiling , Glycogen Synthase Kinase 3/genetics , Glycogen Synthase Kinase 3 beta , Mice , Mice, Inbred ICR , Microdissection/methods , Oligonucleotide Array Sequence Analysis , Organ Culture Techniques , Signal Transduction
8.
J Dent Res ; 90(9): 1070-7, 2011 Sep.
Article in English | MEDLINE | ID: mdl-21487116

ABSTRACT

Salivary glands form during embryonic development by a complex process that creates compact, highly organized secretory organs with functions essential for oral health. The architecture of these glands is generated by branching morphogenesis, revealed by recent research to involve unexpectedly dynamic cell motility and novel regulatory pathways. Numerous growth factors, extracellular matrix molecules, gene regulatory pathways, and mechanical forces contribute to salivary gland morphogenesis, but local gene regulation and morphological changes appear to play particularly notable roles. Here we review these recent advances and their potential application to salivary gland tissue engineering.


Subject(s)
Organogenesis/physiology , Salivary Glands/embryology , Animals , Cell Adhesion Molecules/physiology , Cell Movement , Epithelial Cells/physiology , Extracellular Matrix Proteins/physiology , Fibronectins/physiology , Gene Expression Regulation, Developmental , Growth Substances/physiology , Humans , Intracellular Signaling Peptides and Proteins/physiology , Matrix Metalloproteinase 15/metabolism , Tissue Engineering , Transcription Factors/physiology , rho-Associated Kinases/metabolism
9.
J Chem Phys ; 127(1): 014313, 2007 Jul 07.
Article in English | MEDLINE | ID: mdl-17627352

ABSTRACT

High resolution infrared spectra of the nu(4) fundamental antisymmetric stretching mode and associated hot bands of the linear carbon cluster C(7) were recorded using a tunable diode laser spectrometer in the frequency range of 2135-2141 cm(-1). Spectra of the nu(4) fundamental, nu(4)+nu(11)-nu(11), nu(4)+2nu(11)-2nu(11), and nu(4)+nu(8)-nu(8), bands have been analyzed and are compared to recent experimental results and high level ab initio calculations. In particular, the presented results give experimental evidence for the rigidity of C(7) and confirm theoretical predictions of a rather regular chain molecule, similar to the cases of C(4), C(5), and C(9). For the two energetically low-lying bending modes, nu(8) and nu(11), the rotational constants differ by less than 0.2%, from the ground state value, B(0)=0.030 624 4(28) cm(-1), in good agreement with the recent calculations by Botschwina [Chem. Phys. Lett. 354, 148 (2002)]. From the hot band analysis and the [script-l]-type doubling constant q, experimental values for the band origins of the nu(8) and nu(11) fundamentals have been derived.

10.
Braz. j. med. biol. res ; 36(8): 959-966, Aug. 2003. ilus, tab
Article in English | LILACS | ID: lil-340797

ABSTRACT

Integrins play crucial roles in cell adhesion, migration, and signaling by providing transmembrane links between the extracellular matrix and the cytoskeleton. Integrins cluster in macromolecular complexes to generate cell-matrix adhesions such as focal adhesions. In this mini-review, we compare certain integrin-based biological responses and signaling during cell interactions with standard 2D cell culture versus 3D matrices. Besides responding to the composition of the matrix, cells sense and react to physical properties that include three-dimensionality and rigidity. In routine cell culture, fibroblasts and mesenchymal cells appear to use focal adhesions as anchors. They then use intracellular actomyosin contractility and dynamic, directional integrin movements to stretch cell-surface fibronectin and to generate characteristic long fibrils of fibronectin in "fibrillar adhesions". Some cells in culture proceed to produce dense, three-dimensional matrices similar to in vivo matrix, as opposed to the flat, rigid, two-dimensional surfaces habitually used for cell culture. Cells within such more natural 3D matrices form a distinctive class of adhesion termed "3D-matrix adhesions". These 3D adhesions show distinctive morphology and molecular composition. Their formation is heavily dependent on interactions between integrin alpha5ß1 and fibronectin. Cells adhere much more rapidly to 3D matrices. They also show more rapid morphological changes, migration, and proliferation compared to most 2D matrices or 3D collagen gels. Particularly notable are low levels of tyrosine phosphorylation of focal adhesion kinase and moderate increases in activated mitogen-activated protein kinase. These findings underscore the importance of the dimensionality and dynamics of matrix substrates in cellular responses to the extracellular matrix


Subject(s)
Extracellular Matrix , Integrins , Signal Transduction , Cell Adhesion , Cell Culture Techniques , Cell Division , Cell Movement , Fibronectins
11.
Braz J Med Biol Res ; 36(8): 959-66, 2003 Aug.
Article in English | MEDLINE | ID: mdl-12886449

ABSTRACT

Integrins play crucial roles in cell adhesion, migration, and signaling by providing transmembrane links between the extracellular matrix and the cytoskeleton. Integrins cluster in macromolecular complexes to generate cell-matrix adhesions such as focal adhesions. In this mini-review, we compare certain integrin-based biological responses and signaling during cell interactions with standard 2D cell culture versus 3D matrices. Besides responding to the composition of the matrix, cells sense and react to physical properties that include three-dimensionality and rigidity. In routine cell culture, fibroblasts and mesenchymal cells appear to use focal adhesions as anchors. They then use intracellular actomyosin contractility and dynamic, directional integrin movements to stretch cell-surface fibronectin and to generate characteristic long fibrils of fibronectin in "fibrillar adhesions". Some cells in culture proceed to produce dense, three-dimensional matrices similar to in vivo matrix, as opposed to the flat, rigid, two-dimensional surfaces habitually used for cell culture. Cells within such more natural 3D matrices form a distinctive class of adhesion termed "3D-matrix adhesions". These 3D adhesions show distinctive morphology and molecular composition. Their formation is heavily dependent on interactions between integrin alpha 5 beta 1 and fibronectin. Cells adhere much more rapidly to 3D matrices. They also show more rapid morphological changes, migration, and proliferation compared to most 2D matrices or 3D collagen gels. Particularly notable are low levels of tyrosine phosphorylation of focal adhesion kinase and moderate increases in activated mitogen-activated protein kinase. These findings underscore the importance of the dimensionality and dynamics of matrix substrates in cellular responses to the extracellular matrix.


Subject(s)
Extracellular Matrix/physiology , Integrins/physiology , Signal Transduction/physiology , Cell Adhesion/physiology , Cell Culture Techniques/methods , Cell Division/physiology , Cell Movement/physiology , Fibronectins/physiology , Humans , Imaging, Three-Dimensional
12.
Tissue Eng ; 8(5): 871-8, 2002 Oct.
Article in English | MEDLINE | ID: mdl-12459066

ABSTRACT

An essential structural feature of fluid-secreting epithelial tissues is the presence of tight junctions. To develop a tissue-engineered organ capable of fluid secretion, the cellular component must establish these structures. As part of efforts to create an engineered artificial salivary gland, we have examined the ability of a candidate allogeneic graft cell line, HSG, to produce several key tight junction proteins, as well as to exhibit functional activities consistent with effective tight junction strand formation. In contrast to results obtained with a control kidney cell line, MDCK-II, HSG cells were unable to synthesize four important tight junction-associated proteins: ZO-1, occludin, claudin-1, and claudin-2. In addition, unlike MDCK-II cells, HSG cell monolayers could not restrict paracellular permeability. HSG cells were, thus, unable to generate significant transepithelial electrical resistance or serve as an effective barrier to osmotically imposed fluid movement. Furthermore, these two functional activities could not be reconstituted via the stable transfection of HSG cells with cDNAs encoding either claudin-1 or claudin-2. We conclude that because of their inability to form tight junctions, HSG cells are unsuitable for use as an allogeneic graft cell in an artificial salivary fluid secretory device. These studies also emphasize the importance of graft cell selection in artificial organ development, as certain required characteristics may be difficult to reengineer.


Subject(s)
Salivary Glands , Tight Junctions , Tissue Engineering , Cell Line , Cell Transplantation , Claudin-1 , Claudins , Humans , Membrane Proteins/metabolism , Microscopy, Confocal , Microscopy, Fluorescence , Salivary Glands/metabolism , Salivary Glands/transplantation , Salivary Glands/ultrastructure , Tight Junctions/metabolism , Tight Junctions/ultrastructure , Transplantation, Homologous
13.
Tissue Eng ; 8(4): 649-59, 2002 Aug.
Article in English | MEDLINE | ID: mdl-12202004

ABSTRACT

Radiation therapy for cancer in the head and neck region leads to a marked loss of salivary gland parenchyma, resulting in a severe reduction of salivary secretions. Currently, there is no satisfactory treatment for these patients. To address this problem, we are using both tissue engineering and gene transfer principles to develop an orally implantable, artificial fluid-secreting device. In the present study, we examined the tissue compatibility of two biodegradable substrata potentially useful in fabricating such a device. We implanted in Balb/c mice tubular scaffolds of poly-L-lactic acid (PLLA), poly-glycolic acid coated with PLLA (PGA/PLLA), or nothing (sham-operated controls) either beneath the skin on the back, a site widely used in earlier toxicity and biocompatibility studies, or adjacent to the buccal mucosa, a site quite different functionally and immunologically. At 1, 3, 7, 14, and 28 days postimplantation, implant sites were examined histologically, and systemic responses were assessed by conventional clinical chemistry and hematology analyses. Inflammatory responses in the connective tissue were similar regardless of site or type of polymer implant used. However, inflammatory reactions were shorter and without epithelioid and giant cells in sham-operated controls. Also, biodegradation proceeded more slowly with the PLLA tubules than with the PGA/PLLA tubules. No significant changes in clinical chemistry and hematology were seen due to the implantation of tubular scaffolds. These results indicate that the tissue responses to PLLA and PGA/PLLA scaffolds are generally similar in areas subjacent to skin in the back and oral cavity. However, these studies also identified several potentially significant concerns that must be addressed prior to initiating any clinical applications of this device.


Subject(s)
Biocompatible Materials , Lactic Acid/pharmacology , Mouth Mucosa , Polyglycolic Acid/pharmacology , Polymers/pharmacology , Prostheses and Implants , Skin , Animals , Drug Implants , Female , Inflammation/metabolism , Mice , Mice, Inbred BALB C , Mouth Mucosa/cytology , Mouth Mucosa/drug effects , Polyesters , Skin/cytology , Skin/drug effects
14.
Nat Rev Mol Cell Biol ; 2(11): 793-805, 2001 Nov.
Article in English | MEDLINE | ID: mdl-11715046

ABSTRACT

Integrin-mediated cell adhesions provide dynamic, bidirectional links between the extracellular matrix and the cytoskeleton. Besides having central roles in cell migration and morphogenesis, focal adhesions and related structures convey information across the cell membrane, to regulate extracellular-matrix assembly, cell proliferation, differentiation, and death. This review describes integrin functions, mechanosensors, molecular switches and signal-transduction pathways activated and integrated by adhesion, with a unifying theme being the importance of local physical forces.


Subject(s)
Cell Adhesion , Cell Membrane/metabolism , Cell Membrane/physiology , Cytoskeleton/metabolism , Cytoskeleton/physiology , Extracellular Matrix/metabolism , Extracellular Matrix/physiology , Animals , Cell Differentiation , Cell Division , Cell Line , Cells, Cultured , Humans , Microscopy, Fluorescence , Models, Biological , Phosphorylation , Protein Binding , Signal Transduction
15.
Science ; 294(5547): 1708-12, 2001 Nov 23.
Article in English | MEDLINE | ID: mdl-11721053

ABSTRACT

Adhesions between fibroblastic cells and extracellular matrix have been studied extensively in vitro, but little is known about their in vivo counterparts. Here, we characterized the composition and function of adhesions in three-dimensional (3D) matrices derived from tissues or cell culture. "3D-matrix adhesions" differ from focal and fibrillar adhesions characterized on 2D substrates in their content of alpha5beta1 and alphavbeta3 integrins, paxillin, other cytoskeletal components, and tyrosine phosphorylation of focal adhesion kinase (FAK). Relative to 2D substrates, 3D-matrix interactions also display enhanced cell biological activities and narrowed integrin usage. These distinctive in vivo 3D-matrix adhesions differ in structure, localization, and function from classically described in vitro adhesions, and as such they may be more biologically relevant to living organisms.


Subject(s)
Cell Adhesion , Fibroblasts/cytology , Fibroblasts/metabolism , Imaging, Three-Dimensional/methods , 3T3 Cells , Animals , Cell Adhesion/drug effects , Cell Culture Techniques/methods , Cell Division , Cell Movement , Cell Size , Cells, Cultured , Culture Techniques/methods , Cycloheximide/pharmacology , Cytoskeletal Proteins/metabolism , Extracellular Matrix/chemistry , Extracellular Matrix/metabolism , Fibroblasts/chemistry , Fibronectins/metabolism , Fluorescent Antibody Technique, Indirect , Focal Adhesion Kinase 1 , Focal Adhesion Protein-Tyrosine Kinases , Focal Adhesions/chemistry , Focal Adhesions/metabolism , Glutaral/metabolism , Humans , Integrins/metabolism , Mice , Mitogen-Activated Protein Kinases/metabolism , Molecular Conformation , Phosphorylation , Protein-Tyrosine Kinases/metabolism , Time Factors
16.
J Cell Physiol ; 189(1): 1-13, 2001 Oct.
Article in English | MEDLINE | ID: mdl-11573199

ABSTRACT

Cell proliferation is controlled not only by soluble mitogens but also by components of the extracellular matrix (ECM) such as fibronectin, to which cells adhere via the integrin family of transmembrane receptors. Input from both growth factor receptors and integrins is required to stimulate progression through the G1 phase of the cell cycle, via induction of G1 cyclins and suppression of inhibitors of the G1 cyclin-dependent kinases. Extensive crosstalk takes place between integrin and growth factor receptor signaling pathways, and mitogenic signaling is weak and transient in the absence of integrin-mediated cell adhesion. In normal untransformed cells, all of the important mitogenic signal transduction cascades, namely those downstream of the Ras and Rho family small GTPases and the phosphoinositide 3-OH kinase-PKB/Akt pathway, are regulated by integrin-mediated cell adhesion. As a result, these cells are anchorage-dependent for growth. In contrast, constitutive activity of each of these pathways has been reported in cancer cells, which not only reduces their mitogen dependence but also allows these cells to grow in an anchorage-independent fashion.


Subject(s)
Fibronectins/physiology , Integrins/physiology , Animals , Cell Adhesion , Cell Cycle , Cell Division , Cyclin D1/biosynthesis , Cyclin D1/genetics , Humans , Mitogens/physiology , Neoplasms/etiology , Receptors, Growth Factor/physiology , Signal Transduction , Transcription, Genetic , rho GTP-Binding Proteins
17.
J Cell Physiol ; 189(1): 79-90, 2001 Oct.
Article in English | MEDLINE | ID: mdl-11573207

ABSTRACT

Adhesion of human salivary gland (HSG) epithelial cells to fibronectin- or collagen I gel-coated substrates, mediated by beta1 integrins, has been shown to upregulate the expression of more than 30 genes within 3-6 h. Adhesion of HSG cells to fibronectin or collagen I for 6 h also enhanced total protein kinase C (PKC) activity by 1.8-2.3-fold. HSG cells expressed PKC-alpha, gamma, delta, epsilon, mu, and zeta. Adhesion of HSG cells to fibronectin or collagen I specifically activated PKC-gamma and PKC-delta. Cytoplasmic PKC-gamma and PKC-delta became membrane-associated, and immunoprecipitated PKC-gamma and PKC-delta kinase activities were enhanced 2.5-4.0-fold in HSG cells adherent to fibronectin or collagen I. In addition, adhesion of fibronectin-coated beads to HSG monolayers co-aggregated beta1 integrin and PKC-gamma and PKC-delta but not other PKC isoforms. Thus, integrin-dependent adhesion of HSG cells to fibronectin or collagen I activated PKC-gamma and PKC-delta. The role of this PKC upregulation on adhesion-responsive gene expression was then tested. HSG cells were treated with the specific PKC inhibitor bisindolylmaleimide I, cultured on non-precoated, fibronectin- or collagen I-coated substrates, and analyzed for changes in adhesion-responsive gene expression. Bisindolylmaleimide I strongly inhibited the expression of seven adhesion-responsive genes including calnexin, decorin, S-adenosylmethionine decarboxylase, steroid sulfatase, and 3 mitochondrial genes. However, the expression of two adhesion-responsive genes was not affected by bisindolylmaleimide I. Treatment with bisindolylmaleimide I did not affect cell spreading and did not significantly affect the actin cytoskeleton. These data suggest that adhesion of HSG cells to fibronectin or collagen I induces PKC activity and that this induction contributes to the upregulation of a variety of adhesion-responsive genes.


Subject(s)
Cell Adhesion , Collagen/pharmacology , Epithelial Cells/metabolism , Epithelial Cells/physiology , Fibronectins/pharmacology , Protein Kinase C/physiology , Cells, Cultured , Cytoskeleton/ultrastructure , Enzyme Inhibitors/pharmacology , Epithelial Cells/ultrastructure , Extracellular Matrix/metabolism , Focal Adhesions/metabolism , Humans , Indoles/pharmacology , Integrin beta1/physiology , Maleimides/pharmacology , Protein Isoforms/metabolism , Protein Kinase C/antagonists & inhibitors , RNA, Messenger/biosynthesis , Transcriptional Activation , Up-Regulation
18.
J Cell Sci ; 114(Pt 13): 2375-82, 2001 Jul.
Article in English | MEDLINE | ID: mdl-11559746

ABSTRACT

PTEN (also known as MMAC-1 or TEP-1) is one of the most frequently mutated tumor suppressors in human cancer. It is also essential for embryonic development. PTEN functions primarily as a lipid phosphatase to regulate crucial signal transduction pathways; a key target is phosphatidylinositol 3,4,5-trisphosphate. In addition, it displays weak tyrosine phosphatase activity, which may downmodulate signaling pathways that involve focal adhesion kinase (FAK) or Shc. Levels of PTEN are regulated in embryos and adult organisms, and gene-targeting studies demonstrate that it has a crucial role in normal development. Functions for PTEN have been identified in the regulation of many normal cell processes, including growth, adhesion, migration, invasion and apoptosis. PTEN appears to play particularly important roles in regulating anoikis (apoptosis of cells after loss of contact with extracellular matrix) and cell migration. Gene targeting and transient expression studies have provided insight into the specific signaling pathways that regulate these processes. Characterization of the diverse signaling networks modulated by PTEN, as well as the regulation of PTEN concentration, enzymatic activity, and coordination with other phosphatases, should provide intriguing new insight into the biology of normal and malignant cells.


Subject(s)
Phosphoric Monoester Hydrolases/physiology , Tumor Suppressor Proteins/physiology , Apoptosis , Cell Adhesion , Cell Division , Cell Movement , Gene Expression Regulation, Developmental , Humans , PTEN Phosphohydrolase , Phosphoric Monoester Hydrolases/chemistry , Signal Transduction , Tumor Suppressor Proteins/chemistry
19.
Tissue Eng ; 7(4): 405-13, 2001 Aug.
Article in English | MEDLINE | ID: mdl-11506730

ABSTRACT

Extreme salivary hypofunction is a result of tissue damage caused by irradiation therapy for cancer in the head and neck region. Unfortunately, there is no currently satisfactory treatment for this condition that affects up to 40,000 people in the United States every year. As a novel approach to managing this problem, we are attempting to develop an orally implantable, fluid-secreting device (an artificial salivary gland). We are using the well-studied HSG salivary cell line as a potential allogeneic graft cell for this device. One drawback of using a cell line is the potential for malignant transformation. If such an untoward response occurred, the device could be removed. However, in the event that any HSG cells escaped, we wished to provide additional patient protection. Accordingly, we have engineered HSG cells with a hybrid adeno-retroviral vector, AdLTR.CMV-tk, to express the herpes simplex virus thymidine kinase (HSV-tk) suicide gene as a novel safety factor. Cells were grown on plastic plates or on poly-L-lactic acid disks and then transduced with different multiplicities of infection (MOIs) of the hybrid vector. Thereafter, various concentrations of ganciclovir (GCV) were added, and cell viability was tested. Transduced HSG cells expressed HSV-tk and were sensitive to GCV treatment. Maximal effects were seen at a MOI of 10 with 50 microM of GCV, achieving 95% cell killing on the poly-L-lactic acid substrate. These results suggest that engineering the expression of a suicide gene in an allogeneic graft cell may provide additional safety for use in an artificial salivary gland device.


Subject(s)
Artificial Organs , Cell Line , Salivary Glands/transplantation , Tissue Engineering , Bioprosthesis , Genetic Vectors , Humans , Simplexvirus , Thymidine Kinase/genetics , Transplantation, Homologous
20.
J Immunol ; 167(2): 641-5, 2001 Jul 15.
Article in English | MEDLINE | ID: mdl-11441066

ABSTRACT

Chemokine-induced polarization of lymphocytes involves the rapid collapse of vimentin intermediate filaments (IFs) into an aggregate within the uropod. Little is known about the interactions of lymphocyte vimentin with other cytoskeletal elements. We demonstrate that human peripheral blood T lymphocytes express plectin, an IF-binding, cytoskeletal cross-linking protein. Plectin associates with a complex of structural proteins including vimentin, actin, fodrin, moesin, and lamin B in resting peripheral blood T lymphocytes. During chemokine-induced polarization, plectin redistributes to the uropod associated with vimentin and fodrin; their spatial distribution indicates that this vimentin-plectin-fodrin complex provides a continuous linkage from the nucleus (lamin B) to the cortical cytoskeleton. Overexpression of the plectin IF-binding domain in the T cell line Jurkat induces the perinuclear aggregation of vimentin IFs. Plectin is therefore likely to serve as an important organizer of the lymphocyte cytoskeleton and may regulate changes of lymphocyte cytoarchitecture during polarization and extravasation.


Subject(s)
Cytoskeleton/metabolism , Intermediate Filament Proteins/physiology , T-Lymphocytes/cytology , T-Lymphocytes/metabolism , Actins/metabolism , Alternative Splicing , Carrier Proteins/metabolism , Cell Polarity , HeLa Cells , Humans , Intermediate Filament Proteins/biosynthesis , Intermediate Filament Proteins/blood , Intermediate Filament Proteins/genetics , Intermediate Filaments/genetics , Intermediate Filaments/metabolism , Jurkat Cells/metabolism , Lamin Type B , Lamins , Microfilament Proteins/metabolism , Nuclear Proteins/metabolism , Plectin , Pseudopodia/metabolism , Transfection , Vimentin/metabolism
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