4.5 Article

A novel coculture model of HUVECs and HUASMCs by hyaluronic acid micropattern on titanium surface

期刊

JOURNAL OF BIOMEDICAL MATERIALS RESEARCH PART A
卷 102, 期 6, 页码 1950-1960

出版社

WILEY-BLACKWELL
DOI: 10.1002/jbm.a.34867

关键词

coculture; endothelial cells; smooth muscle cells; micropattern; biomaterials

资金

  1. Key Basic Research Project [2011CB606204]
  2. National Natural Science Foundation of China [30870629, 50971107]
  3. Fundamental Research Funds for the Central Universities [SWJTU11ZT11, SWJTU11CX054]
  4. Open Research Fund of State Key Laboratory of Bioelectronics, Southeast University

向作者/读者索取更多资源

Orientation smooth muscle cell environment plays a positive role in the development of a functional, adherent endothelium. Therefore, building an orientation coculture model of endothelial cells (ECs) and smooth muscle cells (SMCs) on biomaterials surface may provide more help for understanding the interaction between the two cells in vitro. In the present study, a SMCs-ColIV-ECs coculture model was built on the hyaluronic acid (HA) patterned titanium (Ti) surface, and compared with the previous SMCs-HAa-ECs model on endothelial cell number, morphology index, nitric oxide (NO), and prostacyclin(2) (PGI(2)) release, anticoagulation property, human umbilical artery smooth muscle cells (HUASMCs) inhibition property and retention under fluid flow shear stress. The result indicated that SMCs-ColIV-ECs model could enhance the number, spreading area, and major/minor index of human umbilical vein endothelial cells (HUVECs), which contributed to the retention of HUVECs on the surface. Greater major/minor index may produce more NO and PGI(2) release, contributing to the anticoagulation property and HUASMCs inhibition property. In summary, this novel SMCs-ColIV-ECs coculture model improved the previous SMCs-HAa-ECs model, and may provide more inspiration for the human vascular intima building on the biomaterials in vitro. (c) 2013 Wiley Periodicals, Inc. J Biomed Mater Res Part A: 102A: 1950-1960, 2014.

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