<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>18(7)</volume><submitter>Kandasamy M</submitter><pubmed_abstract>Members of the transforming growth factor (TGF)-β family govern a wide range of mechanisms in brain development and in the adult, in particular neuronal/glial differentiation and survival, but also cell cycle regulation and neural stem cell maintenance. This clearly created some discrepancies in the field with some studies favouring neuronal differentiation/survival of progenitors and others favouring cell cycle exit and neural stem cell quiescence/maintenance. Here, we provide a unifying hypothesis claiming that through its regulation of neural progenitor cell (NPC) proliferation, TGF-β signalling might be responsible for (i) maintaining stem cells in a quiescent stage, and (ii) promoting survival of newly generated neurons and their functional differentiation. Therefore, we performed a d</pubmed_abstract><journal>Journal of cellular and molecular medicine</journal><pagination>1444-59</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC4124027</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>TGF-beta signalling in the adult neurogenic niche promotes stem cell quiescence as well as generation of new neurons.</pubmed_title><pmcid>PMC4124027</pmcid><pubmed_authors>Reitsamer HA</pubmed_authors><pubmed_authors>Kraus S</pubmed_authors><pubmed_authors>Sander PR</pubmed_authors><pubmed_authors>Bogdahn U</pubmed_authors><pubmed_authors>Kandasamy M</pubmed_authors><pubmed_authors>Lehner B</pubmed_authors><pubmed_authors>Couillard-Despres S</pubmed_authors><pubmed_authors>Ueberham U</pubmed_authors><pubmed_authors>Aigner L</pubmed_authors><pubmed_authors>Marschallinger J</pubmed_authors><pubmed_authors>Rivera FJ</pubmed_authors><pubmed_authors>Trumbach D</pubmed_authors><pubmed_authors>Strauss O</pubmed_authors></additional><is_claimable>false</is_claimable><name>TGF-beta signalling in the adult neurogenic niche promotes stem cell quiescence as well as generation of new neurons.</name><description>Members of the transforming growth factor (TGF)-β family govern a wide range of mechanisms in brain development and in the adult, in particular neuronal/glial differentiation and survival, but also cell cycle regulation and neural stem cell maintenance. This clearly created some discrepancies in the field with some studies favouring neuronal differentiation/survival of progenitors and others favouring cell cycle exit and neural stem cell quiescence/maintenance. Here, we provide a unifying hypothesis claiming that through its regulation of neural progenitor cell (NPC) proliferation, TGF-β signalling might be responsible for (i) maintaining stem cells in a quiescent stage, and (ii) promoting survival of newly generated neurons and their functional differentiation. Therefore, we performed a d</description><dates><release>2014-01-01T00:00:00Z</release><publication>2014 Jul</publication><modification>2026-04-30T13:32:46.028Z</modification><creation>2026-04-07T16:04:25.662Z</creation></dates><accession>S-EPMC4124027</accession><cross_references><pubmed>24779367</pubmed><doi>10.1111/jcmm.12298</doi></cross_references></HashMap>