4.6 Article

Bradykinin increased the permeability of BTB via NOS/NO/ZONAB-mediating down-regulation of claudin-5 and occludin

期刊

出版社

ACADEMIC PRESS INC ELSEVIER SCIENCE
DOI: 10.1016/j.bbrc.2015.06.082

关键词

Bradykinin; Blood-tumor barrier; NOS; ZONAB; Claudin-5; Occludin

资金

  1. Natural Science Foundation of China [81402573, 81372484, 81372682, 81272795, 81272564, 81171131, 81172197]
  2. Shenyang Science and Technology Plan Projects [F13-318-1-16, F13-220-9-15]

向作者/读者索取更多资源

After demonstrating bradykinin (BK) could increase the permeability of blood-tumor barrier (BTB) via opening the tight junction (TJ), and that the possible mechanism is unclear, we demonstrated that BK could increase the expressions of eNOS and nNOS and promote ZONAB translocation into nucleus. NOS inhibitors L-NAME and 7-NI could effectively block the effect of BK on increasing BTB permeability, decreasing the expressions of claudin-5 and occludin and promoting the translocation of ZONAB. Overexpression of ZONAB could significantly enhance BK-mediating BTB permeability. Meanwhile, chromatin immunoprecipitation verified ZONAB interacted with the promoter of claudin-5 and occludin respectively. This study indicated NOS/NO/ZONAB pathway might be involved in BK's increasing the permeability of BTB. (C) 2015 Elsevier Inc. All rights reserved.

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