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Innate immunity and Inflammophagy: Balancing the Defence and Immune Homeostasis.

Swati ChauhanKautilya Kumar JenaSubhash MehtoNishant Ranjan ChauhanRinku SahuKollori DharRina YadavSivaram KrishnaPundrik JaiswalSantosh Chauhan
Published in: The FEBS journal (2021)
Extensive crosstalk exists between autophagy and innate immune signaling pathways. The stimuli that induce pattern recognition receptor (PRR)-mediated innate immune signaling pathways, also upregulate autophagy. The purpose of this increased autophagy is to eliminate the stimuli and/or suppress the inflammatory pathways by targeted degradation of PRRs or intermediary proteins (termed "inflammophagy"). By executing these functions, autophagy dampens excess inflammation triggered by the innate immune signaling pathways. Thus, autophagy helps in the maintenance of the body's innate immune homeostasis to protect from inflammatory and autoimmune diseases. Many autophagy-dependent mechanisms that could control innate immune signaling have been studied over the last few years. However, still, the understanding is incomplete, and studies that are more systematic should be undertaken to delineate the mechanisms of inflammophagy. Here, we discuss the available knowledge of crosstalk between autophagy and PRR signaling pathways.
Keyphrases
  • innate immune
  • signaling pathway
  • oxidative stress
  • cell death
  • endoplasmic reticulum stress
  • induced apoptosis
  • pi k akt
  • epithelial mesenchymal transition
  • healthcare
  • cell proliferation
  • case control