English
 
User Manual Privacy Policy Disclaimer Contact us
  Advanced SearchBrowse

Item

ITEM ACTIONSEXPORT

Released

Journal Article

Integrin-linked kinase regulates the niche of quiescent epidermal stem cells

MPS-Authors

Morgner,  J.
Max Planck Institute for Biology of Ageing, Max Planck Society;

Ghatak,  S.
Max Planck Institute for Biology of Ageing, Max Planck Society;

Jakobi,  T.
Max Planck Institute for Biology of Ageing, Max Planck Society;

Dieterich,  C.
Max Planck Institute for Biology of Ageing, Max Planck Society;

Aumailley,  M.
Max Planck Institute for Biology of Ageing, Max Planck Society;

Wickstrom,  S. A.
Max Planck Institute for Biology of Ageing, Max Planck Society;

Fulltext (public)
There are no public fulltexts available
Supplementary Material (public)
There is no public supplementary material available
Citation

Morgner, J., Ghatak, S., Jakobi, T., Dieterich, C., Aumailley, M., & Wickstrom, S. A. (2015). Integrin-linked kinase regulates the niche of quiescent epidermal stem cells. Nat Commun, 6, 8198. doi:10.1038/ncomms9198.


Cite as: http://hdl.handle.net/11858/00-001M-0000-002A-CA5C-A
Abstract
Stem cells reside in specialized niches that are critical for their function. Quiescent hair follicle stem cells (HFSCs) are confined within the bulge niche, but how the molecular composition of the niche regulates stem cell behaviour is poorly understood. Here we show that integrin-linked kinase (ILK) is a key regulator of the bulge extracellular matrix microenvironment, thereby governing the activation and maintenance of HFSCs. ILK mediates deposition of inverse laminin (LN)-332 and LN-511 gradients within the basement membrane (BM) wrapping the hair follicles. The precise BM composition tunes activities of Wnt and transforming growth factor-beta pathways and subsequently regulates HFSC activation. Notably, reconstituting an optimal LN microenvironment restores the altered signalling in ILK-deficient cells. Aberrant stem cell activation in ILK-deficient epidermis leads to increased replicative stress, predisposing the tissue to carcinogenesis. Overall, our findings uncover a critical role for the BM niche in regulating stem cell activation and thereby skin homeostasis.