期刊
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS
卷 418, 期 4, 页码 603-608出版社
ACADEMIC PRESS INC ELSEVIER SCIENCE
DOI: 10.1016/j.bbrc.2012.01.043
关键词
MAPK; ERK5; Western blot; Mobility shift; Viral transduction; IR injury
资金
- NIH [RO1GM086401]
- Grants-in-Aid for Scientific Research [22791433] Funding Source: KAKEN
ERK5, a member of the mitogen activated protein kinase, expressed in the kidneys was smaller (similar to 80 kDa) in apparent molecular mass compared to other organs (similar to 120 kDa). A blocking peptide experiment confirmed that the similar to 80 kDa detected on Western blots was a specific band detected by the anti-ERK5 antibody. Expression of the known ERK5 variants ERK5a, b, c, and T confirmed that none of the known splice variants encoded for the renal-specific similar to 80 kDa protein. However, RT-PCR with primers targeting the potential splice sites did not reveal a novel transcript in the kidney. The smaller molecular mass of the kidney-specific ERK5-immunoreactive protein suggested that this cyto-protective molecule may not be fully functional in the kidneys. Lentivirus-mediated in vivo overexpression of full length ERK5 in the mouse kidneys provided protection against renal IR injury. The identity of the renal-specific similar to 80 kDa ERK5 remains unknown but a better understanding of the ERK5 expression and post-translational processing in the kidneys may reveal a novel strategy for renal protection. (C) 2012 Elsevier Inc. All rights reserved.
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