TY - JOUR
T1 - Lunatic fringe-mediated notch signaling regulates adult hippocampal neural stem cell maintenance
AU - Semerci, Fatih
AU - Tin-Shing Choi, William
AU - Bajic, Aleksandar
AU - Thakkar, Aarohi
AU - Encinas, Juan Manuel
AU - Depreux, Frederic
AU - Segil, Neil
AU - Groves, Andrew K.
AU - Maletic-Savatic, Mirjana
N1 - Publisher Copyright:
© 2017, eLife Sciences Publications Ltd. All rights reserved.
PY - 2017/7/12
Y1 - 2017/7/12
N2 - Hippocampal neural stem cells (NSCs) integrate inputs from multiple sources to balance quiescence and activation. Notch signaling plays a key role during this process. Here, we report that Lunatic fringe (Lfng), a key modifier of the Notch receptor, is selectively expressed in NSCs. Further, Lfng in NSCs and Notch ligands Delta1 and Jagged1, expressed by their progeny, together influence NSC recruitment, cell cycle duration, and terminal fate. We propose a new model in which Lfng-mediated Notch signaling enables direct communication between a NSC and its descendants, so that progeny can send feedback signals to the ‘mother’ cell to modify its cell cycle status. Lfng-mediated Notch signaling appears to be a key factor governing NSC quiescence, division, and fate.
AB - Hippocampal neural stem cells (NSCs) integrate inputs from multiple sources to balance quiescence and activation. Notch signaling plays a key role during this process. Here, we report that Lunatic fringe (Lfng), a key modifier of the Notch receptor, is selectively expressed in NSCs. Further, Lfng in NSCs and Notch ligands Delta1 and Jagged1, expressed by their progeny, together influence NSC recruitment, cell cycle duration, and terminal fate. We propose a new model in which Lfng-mediated Notch signaling enables direct communication between a NSC and its descendants, so that progeny can send feedback signals to the ‘mother’ cell to modify its cell cycle status. Lfng-mediated Notch signaling appears to be a key factor governing NSC quiescence, division, and fate.
UR - https://www.scopus.com/pages/publications/85026773435
U2 - 10.7554/eLife.24660
DO - 10.7554/eLife.24660
M3 - Article
C2 - 28699891
AN - SCOPUS:85026773435
SN - 2050-084X
VL - 6
JO - eLife
JF - eLife
M1 - e24660
ER -