Coating of Polystyrene Surface with REDV-Gelatin Conjugate for Selective Isolation of Endothelial Cells

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Endothelial cells (EC), which line the internal surface of blood vessels, play various essential roles in controlling vascular function. The mouse is an important animal model for the study of vascular biology and cardiovascular diseases. However, the isolation of primary EC from the murine aorta is challenging because they are readily contaminated by smooth muscle cells (SMC). A previous study developed a simple method to isolate murine EC from SMC. By taking advantage of the differential sedimentation rate between the two cells, the EC was selectively enriched with collagen-coated polystyrene surfaces. Our study further improved this method by introducing a biomimetic peptide REDV (Arg-Glu-Asp-Val), which may bind specifically to EC but not to SMC or fibroblasts. Firstly, REDV-gelatin conjugate was synthesized by using the amine-to-sulfhydryl crosslinker SMCC. REDV-gelatin coating was then prepared on polystyrene surfaces, and their affinities to EC and SMC were subsequently investigated. Fluorescence microscopy and flow cytometric analysis showed that EC adhesion to the gelatin coating was significantly promoted by REDV peptide conjugation. Moreover, cell migration assay and cell viability assay also showed that the conjugation of REDV does not affect EC migration, and this coating did not show cytotoxicity against EC. This gelatin-REDV coating provides a cost-effective and straightforward tool for isolating EC from SMC, which may facilitate in vitro investigations of EC from mice.

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287-292

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November 2021

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© 2021 Trans Tech Publications Ltd. All Rights Reserved

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[1] A. Bikfalvi. History and conceptual developments in vascular biology and angiogenesis research: a personal view. Angiogenesis, 2017, 20(4): 463-478.

DOI: 10.1007/s10456-017-9569-2

Google Scholar

[2] A.N. Stratman, G.E. Davis. Endothelial cell-pericyte interactions stimulate basement membrane matrix assembly: influence on vascular tube remodeling, maturation, and stabilization[J]. Microsc Microanal, 2012, 18(1): 68-80.

DOI: 10.1017/s1431927611012402

Google Scholar

[3] A.N. Stratman, K.M. Malotte, R.D. Mahan, et al. Pericyte recruitment during vasculogenic tube assembly stimulates endothelial basement membrane matrix formation[J]. Blood, 2009, 114(24): 5091-5101.

DOI: 10.1182/blood-2009-05-222364

Google Scholar

[4] K. Mika, I. Kenji, W. Eiji, et, al. A Simple Method of Isolating Mouse Aortic Endothelial Cells[J]. Journal of Atherosclerosis and Thrombosis,2004,12(3):139-142.

Google Scholar

[5] X. Hao, Q. Li, J. Lv, et al. CREDVW-Linked Polymeric Micelles As a Targeting Gene Transfer Vector for Selective Transfection and Proliferation of Endothelial Cells[J]. ACS applied materials & interfaces, 2015, 7(22): 12128-40.

DOI: 10.1021/acsami.5b02399

Google Scholar

[6] Y. Shan, B. Jia, M. Ye, et al. Application of Heparin/Collagen-REDV Selective Active Interface on ePTFE Films to Enhance Endothelialization and Anticoagulation[J]. Artificial organs, 2018, 42(8): 824-834.

DOI: 10.1111/aor.13131

Google Scholar

[7] Y. Wei, Y. Ji, L. Xiao, et al. Different complex surfaces of polyethyleneglycol (PEG) and REDV ligand to enhance the endothelial cells selectivity over smooth muscle cells[J]. Colloids and surfaces B, Biointerfaces, 2011, 84(2): 369-78.

DOI: 10.1016/j.colsurfb.2011.01.028

Google Scholar