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1.
Biomacromolecules ; 13(5): 1259-68, 2012 May 14.
Article in English | MEDLINE | ID: mdl-22423652

ABSTRACT

Wound healing is a complex process initiated by the formation of fibrin fibers and endothelialization. Normally, this process is triggered in a wound by thrombin cleavage of fibrinopeptides on fibrinogen molecules, which allows them to self spontaneously-assemble into large fibers that provide the support structure of the clot and promote healing. We have found that the fibrous structures can also form without thrombin on most polymer or metal surfaces, including those commonly used for stents. We show that the relatively hydrophobic E and D regions of the fibrinogen molecule are adsorbed on these surfaces, exposing the αC domains, which in turn results in the formation of large fiber structures that promote endothelial cell adhesion. We show that the entire process can be suppressed when stents or other substrates are coated with polymers that are functionalized to bind the αC domains, leading to the development of potentially nonthrombogenic implant materials.


Subject(s)
Anticoagulants/chemical synthesis , Fibrin/chemistry , Fibrin/chemical synthesis , Fibrinogen/chemistry , Fibrinogen/chemical synthesis , Adsorption , Anticoagulants/chemistry , Cell Adhesion/drug effects , Endothelial Cells/drug effects , Particle Size , Protein Conformation , Surface Properties , Time Factors
2.
Biomaterials ; 32(31): 7831-8, 2011 Nov.
Article in English | MEDLINE | ID: mdl-21820169

ABSTRACT

We have investigated the effects of moderate static magnetic fields (SMFs) on murine MC3T3-E1 osteoblasts, and found that they enhance proliferations and promote differentiation. The increase in proliferation rates in response to SMFs was greater in cultures grown on partially sulfonated polytstyrene (SPS, degree of sulfonation: 33%) than in cultures grown on tissue culture plastic. We have previously shown that when the degree of sulfonation exceeded a critical value (12%) [1], spontaneous fibrillogenesis occured which allowed for direct observation of the ECM fibrillar organization under the influence of external fields. We found that the ECM produced in cultures grown on the SPS in the presence of the SMFs assembled into a lattice with larger dimensions than the ECM of the cultures grown in the absence of SMFs. During the early stages of the biomineralization process (day 7), the SMF exposed cultures also templated mineral deposition more rapidly than the control cultures. The rapid response is attributed to orientation of diamagnetic ECM proteins already present in the serum, which could then initiate further cellular signaling. SMFs also influenced late stage osteoblast differentiation as measured by the increased rate of osteocalcin secretion and gene expression beginning 15 days after SFM exposure. This correlated with a large increase in mineral deposition, and in cell modulus. GIXD and EDXS analysis confirmed early deposition of crystalline hydroxyapatite. Previous studies on the effects of moderate SMF had focused on cellular gene and protein expression, but did not consider the organization of the ECM fibers. Our ability to form these fibers has allowed us explore this additional effect and highlight its significance in the initiation of the biomineralization process.


Subject(s)
Calcification, Physiologic/drug effects , Magnetic Fields , Osteoblasts/drug effects , Osteoblasts/metabolism , Polystyrenes/pharmacology , Sulfonic Acids/pharmacology , Animals , Biomechanical Phenomena/drug effects , Cell Line , Cell Proliferation/drug effects , Cell Shape/drug effects , Crystallization , Extracellular Matrix/drug effects , Extracellular Matrix/metabolism , Extracellular Matrix/ultrastructure , Gene Expression Regulation/drug effects , Mice , Microscopy, Scanning Probe , Osteoblasts/cytology , Osteoblasts/ultrastructure , Synchrotrons
3.
J Struct Biol ; 170(1): 83-92, 2010 Apr.
Article in English | MEDLINE | ID: mdl-20035875

ABSTRACT

The extracellular matrix (ECM) is composed of mixed protein fibers whose precise composition affects biomineralization. New methods are needed to probe the interactions of these proteins with calcium phosphate mineral and with each other. Here we follow calcium phosphate mineralization on protein fibers self-assembled in vitro from solutions of fibronectin, elastin and their mixture. We probe the surface morphology and mechanical properties of the protein fibers during the early stages. The development of mineral crystals on the protein matrices is also investigated. In physiological mineralization solution, the elastic modulus of the fibers in the fibronectin-elastin mixture increases to a greater extent than that of the fibers from either pure protein. In the presence of fibronectin, longer exposure in the mineral solution leads to the formation of amorphous calcium phosphate particles templated along the self-assembled fibers, while elastin fibers only collect calcium without any mineral observed during early stage. TEM images confirm that small needle-shape crystals are confined inside elastin fibers which suppress the release of mineral outside the fibers during late stage, while hydroxyapatite crystals form when fibronectin is present. These results demonstrate complementary actions of the two ECM proteins fibronectin and elastin to collect cations and template mineral, respectively.


Subject(s)
Calcification, Physiologic/physiology , Calcium Phosphates/metabolism , Elastin/metabolism , Extracellular Matrix Proteins/metabolism , Fibronectins/metabolism , Microscopy, Confocal , Microscopy, Electron , X-Ray Diffraction
4.
Tissue Eng Part A ; 15(2): 355-66, 2009 Feb.
Article in English | MEDLINE | ID: mdl-18759666

ABSTRACT

Understanding how biomineralization occurs in the extracellular matrix (ECM) of bone cells is crucial to the understanding of bone formation and the development of a successfully engineered bone tissue scaffold. It is still unclear how ECM mechanical properties affect protein-mineral interactions in early stages of bone mineralization. We investigated the longitudinal mineralization properties of MC3T3-E1 cells and the elastic modulus of their ECM using shear modulation force microscopy, synchrotron grazing incidence X-ray diffraction (GIXD), scanning electron microscopy, energy dispersive X-ray spectroscopy, and confocal laser scanning microscopy (CLSM). The elastic modulus of the ECM fibers underwent significant changes for the mineralizing cells, which were not observed in the nonmineralizing cells. On substrates conducive to ECM network production, the elastic modulus of mineralizing cells increased at time points corresponding to mineral production, whereas that of the nonmineralizing cells did not vary over time. The presence of hydroxyapatite in mineralizing cells and the absence thereof in the nonmineralizing ones were confirmed by GIXD, and CLSM showed that a restructuring of actin occurred only for mineral-producing cells. These results show that the correct and complete development of the ECM network is required for osteoblasts to mineralize. This in turn requires a suitably prepared synthetic substrate for bone development to succeed in vitro.


Subject(s)
Bone and Bones/physiology , Calcification, Physiologic/physiology , Extracellular Matrix/metabolism , Tissue Engineering , Animals , Bone and Bones/cytology , Calcium/metabolism , Cell Line , Cell Nucleus/metabolism , Cell Shape , Elastic Modulus , Mice , Microscopy, Atomic Force , Microscopy, Confocal , Osteoblasts/cytology , Osteoblasts/metabolism , Osteoblasts/ultrastructure , Phosphates/metabolism , Synchrotrons
5.
Sheng Wu Yi Xue Gong Cheng Xue Za Zhi ; 22(4): 857-9, 2005 Aug.
Article in Chinese | MEDLINE | ID: mdl-16156290

ABSTRACT

Glass ionomer Cement (GIC) is a kind of new dental restorative material. At present, GIC is finding wider use in dental clinical practice such as restoration, adhesion, cavity liner, cure of dental sensitivity and temporary restoration of cavity, because it has several excellent advantages of strong adhesive strength, low stimulation, inhibition of carious teeth. In this paper, the history of glass ionomer cement is introduced and the researching development and perspective of modified glass ionomer cement is elaborated.


Subject(s)
Dental Restoration, Permanent/methods , Glass Ionomer Cements/chemistry , Dental Bonding , Humans , Root Canal Filling Materials/chemistry , Tensile Strength
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