Skip NavigationSkip to Content

Metabolic but not transcriptional regulation by PKM2 is important for Natural Killer cell responses

  1. Author:
    Walls,Jessica
    Subleski,Jeff
    Palmieri,Erika
    Gonzalez-Cotto,Marieli
    Gardiner, Clair M
    McVicar,Daniel
    Finlay, David K [ORCID]
  2. Author Address

    Laboratory of Cancer Immunometabolism, National Cancer Institute, Frederick, United States., School of Biochemistry and Immunology, Trinity College Dublin, Dublin, Ireland., School of Biochemistry and Immunology and School of Pharmacy and Pharmaceutical Sciences, Trinity College Dublin, Dublin, Ireland.,
    1. Year: 2020
    2. Date: Aug 19
    3. Epub Date: 2020 08 19
  1. Journal: eLife
    1. 9
    2. Pages: pii: e59166
  2. Type of Article: Article
  3. Article Number: e59166
  4. ISSN: 2050-084X
  1. Abstract:

    Natural Killer (NK) cells have an important role in immune responses to viruses and tumours. Integrating changes in signal transduction pathways and cellular metabolism is essential for effective NK cells responses. The glycolytic enzyme Pyruvate Kinase Muscle 2 (PKM2) has described roles in regulating glycolytic flux and signal transduction, particularly gene transcription. While PKM2 expression is robustly induced in activated NK cells, mice lacking PKM2 in NK cells showed no defect in NK cell metabolism, transcription or anti-viral responses to MCMV infection. NK cell metabolism was maintained due to compensatory PKM1 expression in PKM2-null NK cells. To further investigate the role of PKM2 we used TEPP-46, which increases PKM2 catalytic activity while inhibiting any PKM2 signalling functions. NK cells activated with TEPP-46 had reduced effector function due to TEPP-46-induced increases in oxidative stress. Overall, PKM2-regulated glycolytic metabolism and redox status, not transcriptional control, facilitate optimal NK cells responses.

    See More

External Sources

  1. DOI: 10.7554/eLife.59166
  2. PMID: 32812866
  3. WOS: 000569146500001
  4. PII : 59166

Library Notes

  1. Fiscal Year: FY2019-2020
NCI at Frederick

You are leaving a government website.

This external link provides additional information that is consistent with the intended purpose of this site. The government cannot attest to the accuracy of a non-federal site.

Linking to a non-federal site does not constitute an endorsement by this institution or any of its employees of the sponsors or the information and products presented on the site. You will be subject to the destination site's privacy policy when you follow the link.

ContinueCancel