Abstract
ERK5, a member of the mitogen activated protein kinase, expressed in the kidneys was smaller (~80. kDa) in apparent molecular mass compared to other organs (~120. kDa). A blocking peptide experiment confirmed that the ~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 ~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 ~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.
Original language | English |
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Pages (from-to) | 603-608 |
Number of pages | 6 |
Journal | Biochemical and Biophysical Research Communications |
Volume | 418 |
Issue number | 4 |
DOIs | |
Publication status | Published - Feb 24 2012 |
Keywords
- ERK5
- IR injury
- MAPK
- Mobility shift
- Viral transduction
- Western blot
ASJC Scopus subject areas
- Biophysics
- Biochemistry
- Molecular Biology
- Cell Biology