Bone marrow mesenchymal stem cells and type Ⅱ collagen-modified PLGA observation of adhesion.docVIP
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Bone marrow mesenchymal stem cells and type Ⅱ collagen-modified PLGA observation of adhesion
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Bone marrow mesenchymal stem cells and type Ⅱ collagen-modified PLGA observation of adhesion
Abstract Optimization of bone marrow mesenchymal stem cells (bone marrow mesenchymal stem cells, BMSCs) in vitro isolation and culture techniques, improved bio-poly glycolic acid - lactic acid copolymers (poly lactide co glycolide, PLGA) of the cell adhesion was observed BMSCs and Ⅱ type I collagen-modified PLGA of adhesion. [Methods] density gradient centrifugation BMSCs, flow cytometry analysis (FACS) on the cell surface antigen, cell viability, cell cycle detection, phase-contrast microscope observation of cell morphology. Phase separation method to do PLGA, Ⅱ collagen surface modification, taking the third generation of stem cells and PLGA echo, scanning electron microscopy of cell adhesion and materials. [Results] BMSCs can be isolated in vitro amplification, expression CD29, CD44 and CD106, did not express CD34 and CD45, cell viability of 88.96%, G0 G1 cells accounted for 90.32%. The length of spindle cell morphology, Ⅱ collagen surface modification of PLGA average pore size of 100 μm, with BMSCs have better adhesion. [Conclusion] BMSCs in vitro long-term, stable and training, is an ideal seed cells for tissue engineering. Type Ⅱ collagen-modified PLGA surface with the stem cells have better adhesion can be used for tissue engineering of biological materials.
Keywords: bone marrow mesenchymal stem cells in PLGA tissue engineering
Abstract: [Objective] To explore a method for isolating and culturing bone marrow mesenchymal stem cell (BMSCs) in vitro, and improve the cellular conglutination ability of biomaterial poly lactide co glycolic acid (PLGA), and observer the adhesion of BMSCs cultured on PLGA modified with Ⅱ collagen. [Method] BMSCs were isolated and cultured in vitro.The cell exterior antigen, cell livingness and cell cycle were analyzed by flow cytometry method, and cellular configuration was obser
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