Lineage-guided Notch-dependent gliogenesis by Drosophila multi-potent progenitors

Author:

Ren Qingzhong1ORCID,Awasaki Takeshi12,Wang Yu-Chun13,Huang Yu-Fen1ORCID,Lee Tzumin1ORCID

Affiliation:

1. Howard Hughes Medical Institute, Janelia Research Campus, 19700 Helix Drive, Ashburn, VA, USA

2. Current address: Kyorin University School of Medicine, 6-20-2 Shinkawa, Mitaka, Tokyo 181-8611, Japan

3. Current address: 1. VIB Center for the Biology of Disease, 2. K.U. Leuven, Center for Human Genetics, Herestraat 49, 3000 Leuven, Belgium

Abstract

Macroglial cells in the central nervous system exhibit regional specialization and carry out region-specific functions. Diverse glial cells arise from specific progenitors in specific spatiotemporal patterns. This raises an interesting possibility that there exist glial precursors with distinct developmental fates, which govern region-specific gliogenesis. Here we mapped the glial progeny produced by the Drosophila type II neuroblasts, which, like vertebrate radial glia cells, yield both neurons and glia via intermediate neural progenitors (INPs). Distinct type II neuroblasts produce different characteristic sets of glia. A single INP can make both astrocyte-like and ensheathing glia, which co-occupy a relatively restrictive subdomain. Blocking apoptosis uncovers further lineage distinctions in the specification, proliferation, and survival of glial precursors. Both the switch from neurogenesis to gliogenesis and the subsequent glial expansion depend on Notch signaling. Taken together, lineage origins preconfigure the development of individual glial precursors with involvement of serial Notch actions in promoting gliogenesis.

Funder

Howard Hughes Medical Institute

Publisher

The Company of Biologists

Subject

Developmental Biology,Molecular Biology

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