4.8 Article

Lactate dehydrogenase activity drives hair follicle stem cell activation

Journal

NATURE CELL BIOLOGY
Volume 19, Issue 9, Pages 1017-+

Publisher

NATURE PUBLISHING GROUP
DOI: 10.1038/ncb3575

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Funding

  1. Eli and Edythe Broad Center for Regenerative Medicine at UCLA
  2. Tumor Cell Biology programme at UCLA (NIH)
  3. CIRM
  4. New Idea Award from the Leukemia Lymphoma Society
  5. Jonsson Comprehensive Cancer Center
  6. UCLA Clinical Translational Science Institute [UL1TR000124]
  7. Prostate Cancer SPORE at UCLA [P50 CA092131]
  8. Eli & Edythe Broad Center for Regenerative Medicine & Stem Cell Research
  9. UCLA Scholars in Oncologic Molecular Imagining program (NCI/NIH) [R25T CA098010]
  10. UCLA Dissertation Year Fellowship
  11. National Institute of General Medical Sciences [R01-GM081686, R01-GM0866465]
  12. NIH [RO1GM094232]
  13. American Cancer Society [RSG-16-111-01-MPC]
  14. Eli & Edythe Broad Center of Regenerative Medicine and Stem Cell Research at UCLA
  15. Rose Hills Foundation Research Award
  16. NIH-NIAMS [5R01AR57409]
  17. Impact award from CTSI
  18. Jonsson Comprehensive Cancer Foundation
  19. Gaba Fund through the Eli & Edythe Broad Center of Regenerative Medicine at UCLA

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Although normally dormant, hair follicle stem cells (HFSCs) quickly become activated to divide during a new hair cycle. The quiescence of HFSCs is known to be regulated by a number of intrinsic and extrinsic mechanisms. Here we provide several lines of evidence to demonstrate that HFSCs utilize glycolytic metabolism and produce significantly more lactate than other cells in the epidermis. Furthermore, lactate generation appears to be critical for the activation of HFSCs as deletion of lactate dehydrogenase (Ldha) prevented their activation. Conversely, genetically promoting lactate production in HFSCs through mitochondrial pyruvate carrier 1 (Mpc1) deletion accelerated their activation and the hair cycle. Finally, we identify small molecules that increase lactate production by stimulating Myc levels or inhibiting Mpc1 carrier activity and can topically induce the hair cycle. These data suggest that HFSCs maintain a metabolic state that allows them to remain dormant and yet quickly respond to appropriate proliferative stimuli.

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