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Metabolites released from apoptotic cells act as tissue messengers

(2020) NATURE. 580(7801). p.130-135
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Abstract
Caspase-dependent apoptosis accounts for approximately 90% of homeostatic cell turnover in the body(1), and regulates inflammation, cell proliferation, and tissue regeneration(2-4). How apoptotic cells mediate such diverse effects is not fully understood. Here we profiled the apoptotic metabolite secretome and determined its effects on the tissue neighbourhood. We show that apoptotic lymphocytes and macrophages release specific metabolites, while retaining their membrane integrity. A subset of these metabolites is also shared across different primary cells and cell lines after the induction of apoptosis by different stimuli. Mechanistically, the apoptotic metabolite secretome is not simply due to passive emptying of cellular contents and instead is a regulated process. Caspase-mediated opening of pannexin 1 channels at the plasma membrane facilitated the release of a select subset of metabolites. In addition, certain metabolic pathways continued to remain active during apoptosis, with the release of only select metabolites from a given pathway. Functionally, the apoptotic metabolite secretome induced specific gene programs in healthy neighbouring cells, including suppression of inflammation, cell proliferation, and wound healing. Furthermore, a cocktail of apoptotic metabolites reduced disease severity in mouse models of inflammatory arthritis and lung-graft rejection. These data advance the concept that apoptotic cells are not inert cells waiting for removal, but instead release metabolites as 'good-bye' signals to actively modulate outcomes in tissues. Apoptotic cells communicate with neighbouring cells by the regulated release of specific metabolites, and a cocktail of select apoptotic metabolites reduces disease severity in mouse models of inflammatory arthritis and lung transplant rejection.
Keywords
PANNEXIN 1 CHANNELS, FIND-ME SIGNAL, EXPRESSION, DISEASE, DEATH, BAX

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MLA
Medina, Christopher B., et al. “Metabolites Released from Apoptotic Cells Act as Tissue Messengers.” NATURE, vol. 580, no. 7801, 2020, pp. 130–35, doi:10.1038/s41586-020-2121-3.
APA
Medina, C. B., Mehrotra, P., Arandjelovic, S., Perry, J. S. A., Guo, Y., Morioka, S., … Ravichandran, K. (2020). Metabolites released from apoptotic cells act as tissue messengers. NATURE, 580(7801), 130–135. https://doi.org/10.1038/s41586-020-2121-3
Chicago author-date
Medina, Christopher B., Parul Mehrotra, Sanja Arandjelovic, Justin S.A. Perry, Yizhan Guo, Sho Morioka, Brady Barron, et al. 2020. “Metabolites Released from Apoptotic Cells Act as Tissue Messengers.” NATURE 580 (7801): 130–35. https://doi.org/10.1038/s41586-020-2121-3.
Chicago author-date (all authors)
Medina, Christopher B., Parul Mehrotra, Sanja Arandjelovic, Justin S.A. Perry, Yizhan Guo, Sho Morioka, Brady Barron, Scott F. Walk, Bart Ghesquiere, Ulrike Lorenz, Alexander S. Krupnick, and Kodi Ravichandran. 2020. “Metabolites Released from Apoptotic Cells Act as Tissue Messengers.” NATURE 580 (7801): 130–135. doi:10.1038/s41586-020-2121-3.
Vancouver
1.
Medina CB, Mehrotra P, Arandjelovic S, Perry JSA, Guo Y, Morioka S, et al. Metabolites released from apoptotic cells act as tissue messengers. NATURE. 2020;580(7801):130–5.
IEEE
[1]
C. B. Medina et al., “Metabolites released from apoptotic cells act as tissue messengers,” NATURE, vol. 580, no. 7801, pp. 130–135, 2020.
@article{8663047,
  abstract     = {{Caspase-dependent apoptosis accounts for approximately 90% of homeostatic cell turnover in the body(1), and regulates inflammation, cell proliferation, and tissue regeneration(2-4). How apoptotic cells mediate such diverse effects is not fully understood. Here we profiled the apoptotic metabolite secretome and determined its effects on the tissue neighbourhood. We show that apoptotic lymphocytes and macrophages release specific metabolites, while retaining their membrane integrity. A subset of these metabolites is also shared across different primary cells and cell lines after the induction of apoptosis by different stimuli. Mechanistically, the apoptotic metabolite secretome is not simply due to passive emptying of cellular contents and instead is a regulated process. Caspase-mediated opening of pannexin 1 channels at the plasma membrane facilitated the release of a select subset of metabolites. In addition, certain metabolic pathways continued to remain active during apoptosis, with the release of only select metabolites from a given pathway. Functionally, the apoptotic metabolite secretome induced specific gene programs in healthy neighbouring cells, including suppression of inflammation, cell proliferation, and wound healing. Furthermore, a cocktail of apoptotic metabolites reduced disease severity in mouse models of inflammatory arthritis and lung-graft rejection. These data advance the concept that apoptotic cells are not inert cells waiting for removal, but instead release metabolites as 'good-bye' signals to actively modulate outcomes in tissues.
Apoptotic cells communicate with neighbouring cells by the regulated release of specific metabolites, and a cocktail of select apoptotic metabolites reduces disease severity in mouse models of inflammatory arthritis and lung transplant rejection.}},
  author       = {{Medina, Christopher B. and Mehrotra, Parul and Arandjelovic, Sanja and Perry, Justin S.A. and Guo, Yizhan and Morioka, Sho and Barron, Brady and Walk, Scott F. and Ghesquiere, Bart and Lorenz, Ulrike and Krupnick, Alexander S. and Ravichandran, Kodi}},
  issn         = {{0028-0836}},
  journal      = {{NATURE}},
  keywords     = {{PANNEXIN 1 CHANNELS,FIND-ME SIGNAL,EXPRESSION,DISEASE,DEATH,BAX}},
  language     = {{eng}},
  number       = {{7801}},
  pages        = {{130--135}},
  title        = {{Metabolites released from apoptotic cells act as tissue messengers}},
  url          = {{http://doi.org/10.1038/s41586-020-2121-3}},
  volume       = {{580}},
  year         = {{2020}},
}

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