磷酸化
细胞生物学
化学
生物
分泌物
肿瘤坏死因子α
p38丝裂原活化蛋白激酶
蛋白激酶A
激酶
免疫学
生物化学
作者
Alexey Kotlyarov,Armin Neininger,Carola Schubert,R Eckert,Carmen Birchmeier,Hans‐Dieter Volk,Matthias Gaestel
摘要
MAPKAP kinase 2 (MK2) is one of several kinases that are regulated through direct phosphorylation by p38 MAP kinase. By introducing a targeted mutation into the mouse MK2 gene, we have determined the physiological function of MK2 in vivo. Mice that lack MK2 show increased stress resistance and survive LPS-induced endotoxic shock. This is due to a reduction of approximately 90% in the production of tumor necrosis factor-alpha (TNF-alpha) and not to a change in signalling from the TNF receptor. The level and stability of TNF-alpha mRNA is not reduced and TNF-alpha secretion is not affected. We conclude that MK2 is an essential component in the inflammatory response which regulates biosynthesis of TNF-alpha at a post-transcriptional level.
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