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Cell biology of inflammasome activation

期刊

TRENDS IN CELL BIOLOGY
卷 31, 期 11, 页码 924-939

出版社

CELL PRESS
DOI: 10.1016/j.tcb.2021.06.010

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资金

  1. Australian National University
  2. National Health and Medical Research Council of Australia [APP1141504, APP1162103, APP1163358, APP2002686]
  3. Gretel and Gordon Bootes Medical Research Foundation
  4. John Curtin School of Medical Research International Ph.D. scholarships
  5. CSL Centenary Fellowship

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Organelles play a critical role in regulating and activating inflammasomes in cells, leading to inflammation and cell death. NLRP3 and Pyrin inflammasome sensors may aggregate at the microtubule-organizing center, activating various pathways that result in pyroptosis, cellular disintegration, and inflammation.
Organelles are critical structures in mediating the assembly and activation of inflammasomes in mammalian cells, resulting in inflammation and cell death. Assembly of inflammasomes can occur at the mitochondria, endoplasmic reticulum, nucleus, trans-Golgi network, or pathogen surface, facilitated by the overarching architecture of the cytoskeleton. NLRP3 and Pyrin inflammasome sensors may form smaller speckles and converge on a single larger speck at the microtubule-organizing center (MTOC). This signaling hub activates multiple mammalian inflammatory and apoptotic caspases, cytokine substrates, the pore-forming protein gasdermin D, and the plasma membrane rupture protein ninjurin-1 (NINJ1), allowing pyroptosis, cellular disintegration, and inflammation to ensue. In this review, we highlight the role of mammalian cell types and organellar architectures in executing inflammasome responses.

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