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Necroptosis in development and diseases

期刊

GENES & DEVELOPMENT
卷 32, 期 5-6, 页码 327-340

出版社

COLD SPRING HARBOR LAB PRESS, PUBLICATIONS DEPT
DOI: 10.1101/gad.312561.118

关键词

apoptosis; MLKL; necroptosis; RIPK1; RIPK3

资金

  1. National Key R&D Program of China [2016YFA0501900]
  2. China National Natural Science Foundation [31530041]
  3. Chinese Academy of Sciences
  4. National Institute of Neurological Disorders and Stroke [1R01NS082257]
  5. National Institute on Aging [1R01AG047231, RF1AG055521]
  6. Natural Science Foundation of Shanghai [16ZR1443900]

向作者/读者索取更多资源

Necroptosis, a form of regulated necrotic cell death mediated by RIPK1 (receptor-interacting protein kinase 1) kinase activity, RIPK3, and MLKL (mixed-lineage kinase domain-like pseudokinase), can be activated under apoptosis-deficient conditions. Modulating the activation of RIPK1 by ubiquitination and phosphorylation is critical to control both necroptosis and apoptosis. Mutant mice with kinase-dead RIPK1 or RIPK3 and MLKL deficiency show no detrimental phenotype in regard to development and adult homeostasis. However, necroptosis and apoptosis can be activated in response to various mutations that result in the abortion of the defective embryos and human inflammatory and neurodegenerative pathologies. RIPK1 inhibition represents a key therapeutic strategy for treatment of diseases where blocking both necroptosis and apoptosis can be beneficial.

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