TY - JOUR
T1 - Autophagy regulates Notch degradation and modulates stem cell development and neurogenesis
AU - Wu, Xiaoting
AU - Fleming, Angeleen
AU - Ricketts, Thomas
AU - Pavel, Mariana
AU - Virgin, Herbert
AU - Menzies, Fiona M.
AU - Rubinsztein, David C.
N1 - Funding Information:
We are grateful to the Wellcome Trust (Principal Research Fellowship to DCR, 095317/Z/11/Z), Wellcome Trust Strategic Grant to Cambridge Institute for Medical Research (100140/Z/12/Z), Friedrich-Ebert-Stiftung, NIH grants AI109725 and AI084887 for funding. We are also thankful to Dr Y. Takahashi, Dr T. Yoshimori and Dr D. Kent for providing valuable reagents used in this work.
PY - 2016/2/3
Y1 - 2016/2/3
N2 - Autophagy is a conserved, intracellular, lysosomal degradation pathway. While mechanistic aspects of this pathway are increasingly well defined, it remains unclear how autophagy modulation impacts normal physiology. It is, however, becoming clear that autophagy may play a key role in regulating developmental pathways. Here we describe for the first time how autophagy impacts stem cell differentiation by degrading Notch1. We define a novel route whereby this plasma membrane-resident receptor is degraded by autophagy, via uptake into ATG16L1-positive autophagosome-precursor vesicles. We extend our findings using a physiologically relevant mouse model with a hypomorphic mutation in Atg16L1, a crucial autophagy gene, which shows developmental retention of early-stage cells in various tissues where the differentiation of stem cells is retarded and thus reveal how modest changes in autophagy can impact stem cell fate. This may have relevance for diverse disease conditions, like Alzheimer' s Disease or Crohn' s Disease, associated with altered autophagy.
AB - Autophagy is a conserved, intracellular, lysosomal degradation pathway. While mechanistic aspects of this pathway are increasingly well defined, it remains unclear how autophagy modulation impacts normal physiology. It is, however, becoming clear that autophagy may play a key role in regulating developmental pathways. Here we describe for the first time how autophagy impacts stem cell differentiation by degrading Notch1. We define a novel route whereby this plasma membrane-resident receptor is degraded by autophagy, via uptake into ATG16L1-positive autophagosome-precursor vesicles. We extend our findings using a physiologically relevant mouse model with a hypomorphic mutation in Atg16L1, a crucial autophagy gene, which shows developmental retention of early-stage cells in various tissues where the differentiation of stem cells is retarded and thus reveal how modest changes in autophagy can impact stem cell fate. This may have relevance for diverse disease conditions, like Alzheimer' s Disease or Crohn' s Disease, associated with altered autophagy.
UR - http://www.scopus.com/inward/record.url?scp=84957598643&partnerID=8YFLogxK
U2 - 10.1038/ncomms10533
DO - 10.1038/ncomms10533
M3 - Article
C2 - 26837467
AN - SCOPUS:84957598643
SN - 2041-1723
VL - 7
JO - Nature communications
JF - Nature communications
M1 - 10533
ER -