Enteroendocrine cells are generated from stem cells through a distinct progenitor in the adult Drosophila posterior midgut
Author(s) -
Xiankun Zeng,
Steven X. Hou
Publication year - 2015
Publication title -
development
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.15
H-Index - 36
eISSN - 1477-9129
pISSN - 0950-1991
DOI - 10.1242/dev.113357
Subject(s) - biology , stem cell , enteroendocrine cell , progenitor cell , microbiology and biotechnology , progenitor , cellular differentiation , midgut , adult stem cell , lineage (genetic) , regeneration (biology) , genetics , endocrine system , gene , endocrinology , botany , larva , hormone
Functional mature cells are continually replenished by stem cells to maintain tissue homoeostasis. In the adult Drosophila posterior midgut, both terminally differentiated enterocyte (EC) and enteroendocrine (EE) cells are generated from an intestinal stem cell (ISC). However, it is not clear how the two differentiated cells are generated from the ISC. In this study, we found that only ECs are generated through the Su(H)GBE(+) immature progenitor enteroblasts (EBs), whereas EEs are generated from ISCs through a distinct progenitor pre-EE by a novel lineage-tracing system. EEs can be generated from ISCs in three ways: an ISC becoming an EE, an ISC becoming a new ISC and an EE through asymmetric division, or an ISC becoming two EEs through symmetric division. We further identified that the transcriptional factor Prospero (Pros) regulates ISC commitment to EEs. Our data provide direct evidence that different differentiated cells are generated by different modes of stem cell lineage specification within the same tissues.
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