TRIP6 promotes neural stem cell maintenance through YAP-mediated Sonic Hedgehog activation

• Published in: The FASEB journal Vol. 38; no. 5; p. e23501
• Main Authors: Li, Ming-Yang, Yang, Xiu-Li, Chung, Chia-Chi, Lai, Yun-Ju, Tsai, Jui-Cheng, Kuo, Ya-Lin, Yu, Jenn-Yah, Wang, Tsu-Wei
• Format: Journal Article
• Language: English
• Published: United States 15.03.2024
• Subjects: Animals; Brain; Hedgehog Proteins; Mammals; Mice; Neural Stem Cells; Neurogenesis; Neurons; adult neurogenesis; YAP; SHH; neural stem cell; Hippo pathway; TRIP6
• ISSN: 1530-6860
• DOI: 10.1096/fj.202301805RRR

In the adult mammalian brain, new neurons are continuously generated from neural stem cells (NSCs) in the subventricular zone (SVZ)-olfactory bulb (OB) pathway. YAP, a transcriptional co-activator of the Hippo pathway, promotes cell proliferation and inhibits differentiation in embryonic neural progenitors. However, the role of YAP in postnatal NSCs remains unclear. Here, we showed that YAP was present in NSCs of the postnatal mouse SVZ. Forced expression of Yap promoted NSC maintenance and inhibited differentiation, whereas depletion of Yap by RNA interference or conditional knockout led to the decline of NSC maintenance, premature neuronal differentiation, and collapse of neurogenesis. For the molecular mechanism, thyroid hormone receptor-interacting protein 6 (TRIP6) recruited protein phosphatase PP1A to dephosphorylate LATS1/2, therefore inducing YAP nuclear localization and activation. Moreover, TRIP6 promoted NSC maintenance, cell proliferation, and inhibited differentiation through YAP. In addition, YAP regulated the expression of the Sonic Hedgehog (SHH) pathway effector Gli2 and Gli1/2 mediated the effect of YAP on NSC maintenance. Together, our findings demonstrate a novel TRIP6-YAP-SHH axis, which is critical for regulating postnatal neurogenesis in the SVZ-OB pathway.