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First we eat, then we do everything else: The dynamic metabolic regulation of efferocytosis

期刊

CELL METABOLISM
卷 33, 期 11, 页码 2126-2141

出版社

CELL PRESS
DOI: 10.1016/j.cmet.2021.08.001

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资金

  1. NIH NCI [5R00CA237728-03]
  2. Parker Institute for Cancer Immuno-therapy Career Development Award
  3. V Foundation Scholars Grant
  4. MSKCC Cancer Center Support Grant [P30CA008748]

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Clearance of apoptotic cells, known as efferocytosis, is essential for processes like embryonic development and immune cell development. This process poses intriguing cell metabolism problems where phagocytes like macrophages play a crucial role.
Clearance of apoptotic cells, or efferocytosis,is essential for diverse processes including embryonic development, tissue turnover, organ regeneration, and immune cell development. The human body is estimated to remove approximately 1% of its body mass via apoptotic cell clearance daily. This poses several intriguing cell metabolism problems. For instance, phagocytes such as macrophages must induce or suppress metabolic pathways to find, engulf, and digest apoptotic cells. Then, phagocytes must manage the potentially burdensome biomass of the engulfed apoptotic cell. Finally, phagocytes reside in complex tissue architectures that vary in nutrient availability, the types of dying cells or debris that require clearance, and the neighboring cells they interact with. Here, we review advances in our understanding of these three key areas of phagocyte metabolism. We end by proposing a model of efferocytosis that integrates recent findings and establishes a new paradigm for testing how efferocytosis prevents chronic inflammatory disease and autoimmunity.

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