Premium
Photochemical tissue bonding promotes the proliferation and migration of injured tenocytes through ROS/RhoA/NF‐κB/Dynamin 2 signaling pathway
Author(s) -
Yao Zuochao,
Wang Xi,
Zhang Wen,
Liu Yushu,
Ni Tao
Publication year - 2018
Publication title -
journal of cellular physiology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.529
H-Index - 174
eISSN - 1097-4652
pISSN - 0021-9541
DOI - 10.1002/jcp.26628
Subject(s) - rhoa , microbiology and biotechnology , chemistry , dynamin , nf κb , signal transduction , biology , receptor , endocytosis , biochemistry
Photochemical tissue bonding (PTB) has been found to promote the healing of Achilles tendon tissue injury and to reduce postoperative complications. However, the underlying cellular and molecular mechanisms are not clear. In this study, the cell proliferation, ROS generation, migration and the protein expression of DNM2, NF‐κB p65, TGF‐β1 and VEGF in tenocytes after PTB treatment were measured by CCK‐8, flow cytometry, Transwell and western blot assay, respectively. And those in tenocytes after DNM2 silencing or overexpressing or treatment with inhibitors of NF‐κB, ROS and RhoA were also measured. Our results showed that 10 mW PTB treatment for 80 and 120 s significantly increased cell proliferation and increased ROS generation in tenocytes. 10 mW PTB treatment for 40 and 80 s significantly activated RhoA and increased the protein expression of DNM2, NF‐κB p65, TGF‐β1 and VEGF, but 10 mW PTB treatment for 120 s decreased the protein expression of those. DNM2 silencing significantly suppressed cell migration and the expression of DNM2, TGF‐β1, and VEGF in tenocytes after PTB treatment (10 mW, 80 s), which was inhibited by DNM2 overexpression. Individual treatment with inhibitor of NF‐κB, ROS, and RhoA in tenocytes showed decreased protein expression of DNM2, TGF‐β1, and VEGF. Moreover, in vivo experiment found that PTB treatment significantly inhibited cell apoptosis and the expression of DNM2, NF‐κB p65, RhoA, TGF‐β1, and VEGF in a time‐dependent manner. Taken together, our results suggest that PTB promotes the proliferation and migration of injured tenocytes through ROS/RhoA/NF‐κB/DNM2 signaling pathway.