Pituitary stem cells produce paracrine WNT signals to control the expansion of their descendant progenitor cells
- Others:
- King's College London
- Singapore Institute of Technology [Singapore] (SIT)
- Nanyang Technological University [Singapour]
- University Hospital Carl Gustav Carus [Dresden, Germany] ; Technische Universität Dresden = Dresden University of Technology (TU Dresden)
- Institut de Génomique Fonctionnelle (IGF) ; Institut National de la Santé et de la Recherche Médicale (INSERM)-Université de Montpellier (UM)-Centre National de la Recherche Scientifique (CNRS)
- Stanford University School of Medicine [CA, USA]
- University of California [San Francisco] (UC San Francisco) ; University of California (UC)
- University College of London [London] (UCL)
- Université Côte d'Azur (UCA)
Description
In response to physiological demand, the pituitary gland generates new hormone-secreting cells from committed progenitor cells throughout life. It remains unclear to what extent pituitary stem cells (PSCs), which uniquely express SOX2, contribute to pituitary growth and renewal. Moreover, neither the signals that drive proliferation nor their sources have been elucidated. We have used genetic approaches in the mouse, showing that the WNT pathway is essential for proliferation of all lineages in the gland. We reveal that SOX2+ stem cells are a key source of WNT ligands. By blocking secretion of WNTs from SOX2+ PSCs in vivo, we demonstrate that proliferation of neighbouring committed progenitor cells declines, demonstrating that progenitor multiplication depends on the paracrine WNT secretion from SOX2+ PSCs. Our results indicate that stem cells can hold additional roles in tissue expansion and homeostasis, acting as paracrine signalling centres to coordinate the proliferation of neighbouring cells.
Abstract
International audience
Additional details
- URL
- https://hal.archives-ouvertes.fr/hal-03429076
- URN
- urn:oai:HAL:hal-03429076v1
- Origin repository
- UNICA