Literature DB >> 10383731

Fibrin microbeads (FMB) as biodegradable carriers for culturing cells and for accelerating wound healing.

R Gorodetsky1, R A Clark, J An, J Gailit, L Levdansky, A Vexler, E Berman, G Marx.   

Abstract

We have developed biodegradable fibrin-derived microbeads as potent cell carriers. The fibrin-derived microbeads, 50-200 microm in diameter, were tested for their attachment to a wide range of cell types. Fibrin-derived microbeads were shown to be greatly haptotactic to cells (such as endothelial cells, smooth muscle cells and fibroblasts), which respond to fibrinogen in contrast to keratinocytes and different cell lines derived from leukocytic lineage. The cells on fibrin-derived microbeads could be maintained for more than 10 d and achieved a high density. 31P-nuclear magnetic resonance was employed to monitor phosphate metabolism in cells, with densities on the order of 100 million cells per g of fibrin-derived microbeads. The 31P-nuclear magnetic resonance adenosine triphosphate and phosphocreatine signals, equivalent to the signal obtained with perfused normal skin, indicated that metabolism of cells on fibrin-derived microbeads was responsive to oxygenation and nutrients. Light, fluorescent, and confocal laser microscopy revealed that the porous fibrin-derived microbeads accommodate up to 200-300 cells due to their high surface area which minimized contact inhibition. Cells could degrade the fibrin-derived microbeads and be transferred to seed culture flasks without trypsinization. In a pig skin wound healing model, fibrin-derived microbeads + fibroblasts were transplanted into full thickness punch wounds. This procedure was compared with other treatment modalities, such as the addition of human platelet-derived growth factor BB or fibrin-derived microbeads alone. By the third day after wounding, only the wounds in which fibroblasts on fibrin-derived microbeads were added showed significant formation of granulation tissue. Based on the above, we project many uses of our novel fibrin-derived microbead technology for cell culturing, wound healing and tissue engineering.

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Year:  1999        PMID: 10383731     DOI: 10.1046/j.1523-1747.1999.00600.x

Source DB:  PubMed          Journal:  J Invest Dermatol        ISSN: 0022-202X            Impact factor:   8.551


  21 in total

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3.  Temporal and spatial patterning of transgene expression by near-infrared irradiation.

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4.  Fibrin microbeads loaded with mesenchymal cells support their long-term survival while sealed at room temperature.

Authors:  Raphael Gorodetsky; Lilia Levdansky; Elena Gaberman; Olga Gurevitch; Esther Lubzens; William H McBride
Journal:  Tissue Eng Part C Methods       Date:  2011-05-25       Impact factor: 3.056

5.  Phase-separated chitosan-fibrin microbeads for cell delivery.

Authors:  Zhewei Chen; Limin Wang; Jan P Stegemann
Journal:  J Microencapsul       Date:  2011       Impact factor: 3.142

6.  Physical and biological characterization of ferromagnetic fiber networks: effect of fibrin deposition on short-term in vitro responses of human osteoblasts.

Authors:  Rose L Spear; Brajith Srigengan; Suresh Neelakantan; Wolfram Bosbach; Roger A Brooks; Athina E Markaki
Journal:  Tissue Eng Part A       Date:  2014-10-03       Impact factor: 3.845

7.  Fibrin concentration affects ACL fibroblast proliferation and collagen synthesis.

Authors:  Patrick Vavken; Shilpa M Joshi; Martha M Murray
Journal:  Knee       Date:  2010-01-18       Impact factor: 2.199

8.  Aqueous two-phase deposition and fibrinolysis of fibroblast-laden fibrin micro-scaffolds.

Authors:  Stephen Robinson; Jonathan Chang; Eric Parigoris; Louise Hecker; Shuichi Takayama
Journal:  Biofabrication       Date:  2021-04-07       Impact factor: 9.954

9.  Marrow-derived stromal cell delivery on fibrin microbeads can correct radiation-induced wound-healing deficits.

Authors:  Michael W Xie; Raphael Gorodetsky; Ewa D Micewicz; Ewa D Micevicz; Natalia C Mackenzie; Elena Gaberman; Lilia Levdansky; William H McBride
Journal:  J Invest Dermatol       Date:  2012-09-06       Impact factor: 8.551

10.  Bone progenitors produced by direct osteogenic differentiation of the unprocessed bone marrow demonstrate high osteogenic potential in vitro and in vivo.

Authors:  Irene Ginis; Miron Weinreb; Natalie Abramov; Doron Shinar; Shoshana Merchav; Aharon Schwartz; Mitchell Shirvan
Journal:  Biores Open Access       Date:  2012-04
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