Department of Anesthesiology, University of Wisconsin School of Medicine and Public Health, Madison, WI, United States.
Biochem Biophys Res Commun. 2012 Feb 24;418(4):603-8. doi: 10.1016/j.bbrc.2012.01.043. Epub 2012 Jan 24.
ERK5, a member of the mitogen activated protein kinase, expressed in the kidneys was smaller (∼80kDa) in apparent molecular mass compared to other organs (∼120kDa). A blocking peptide experiment confirmed that the ∼80kDa 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 ∼80kDa 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 ∼80kDa 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.
ERK5 是丝裂原活化蛋白激酶的一个成员,在肾脏中表达,其表观分子量(~80kDa)比其他器官(~120kDa)小。阻断肽实验证实,Western blot 上检测到的~80kDa 是抗 ERK5 抗体特异性检测到的条带。已知的 ERK5 变体 ERK5a、b、c 和 T 的表达证实,已知的剪接变体都没有编码肾脏特异性~80kDa 蛋白。然而,针对潜在剪接位点的 RT-PCR 并未在肾脏中发现新的转录本。肾脏特异性 ERK5 免疫反应性蛋白的较小分子量表明,这种细胞保护分子在肾脏中可能没有完全发挥功能。慢病毒介导的全长 ERK5 在小鼠肾脏中的体内过表达为肾脏缺血再灌注损伤提供了保护。肾脏特异性~80kDa ERK5 的身份仍不清楚,但对肾脏中 ERK5 的表达和翻译后加工的更好理解可能揭示一种新的肾脏保护策略。