Original article (Basic research)

Effect of denatured collagen type Ⅰ on endothelial cell proliferation, migration and angiogenesis-related proteins

  • SU Rong-jia ,
  • WANG Zhi-yong ,
  • WANG Xi-qiao ,
  • LIU Ying-kai ,
  • DONG Jiao-yun ,
  • SONG Fei ,
  • LU Shu-liang
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  • 1. Shanghai Burns Institute, Shanghai 200025, China; 2. Department of Burns and Plastic Surgery, Ruijin Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai 200025, China

Online published: 2020-02-06

Supported by

National Natural Science Foundation of China, 81071567, 30872686, 81000838

Abstract

Objective · To reveal the effect of denatured collagen type Ⅰ on the endothelial cell proliferation, migration, and angiogenesis-related proteins . Methods · Human umbilical vein endothelial cells were cultured on the plates coated with normal collagen (normal collagen group), half concentration normal collagen (half collagen group) or denatured collagen (denatured collagen group). CCK-8 assay was performed to test cell proliferation ability two days later. The effect of collagen on cell migration was measuredscratch test. The s of membrane-type 1 matrix metalloproteinase (MT1-MMP) and vascular endothelial growth factor (VEGF) were detectedWestern blotting. The s of angiopoietin 1 (Ang-1) and Ang-2 were measuredELISA. Results · CCK-8 results showed that the proliferation activity of denatured collagen group was significantly higher than that of normal collagen group and half collagen group (PPPConclusion · Denatured collagen type Ⅰ can promote proliferation, migration and MT1-MMP, VEGF, and Ang-2 s in endothelial cells, suggesting that collagen denaturation may play an active role in the process of angiogenesis during wound healing.

Cite this article

SU Rong-jia , WANG Zhi-yong , WANG Xi-qiao , LIU Ying-kai , DONG Jiao-yun , SONG Fei , LU Shu-liang . Effect of denatured collagen type Ⅰ on endothelial cell proliferation, migration and angiogenesis-related proteins[J]. Journal of Shanghai Jiao Tong University (Medical Science), 2019 , 39(12) : 1348 . DOI: 10.3969/j.issn.1674-8115.2019.12.002

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