» Articles » PMID: 25249462

Ascl1 Controls the Number and Distribution of Astrocytes and Oligodendrocytes in the Gray Matter and White Matter of the Spinal Cord

Overview
Journal Development
Specialty Biology
Date 2014 Sep 25
PMID 25249462
Citations 21
Authors
Affiliations
Soon will be listed here.
Abstract

Glia constitute the majority of cells in the mammalian central nervous system and are crucial for neurological function. However, there is an incomplete understanding of the molecular control of glial cell development. We find that the transcription factor Ascl1 (Mash1), which is best known for its role in neurogenesis, also functions in both astrocyte and oligodendrocyte lineages arising in the mouse spinal cord at late embryonic stages. Clonal fate mapping in vivo reveals heterogeneity in Ascl1-expressing glial progenitors and shows that Ascl1 defines cells that are restricted to either gray matter (GM) or white matter (WM) as astrocytes or oligodendrocytes. Conditional deletion of Ascl1 post-neurogenesis shows that Ascl1 is required during oligodendrogenesis for generating the correct numbers of WM but not GM oligodendrocyte precursor cells, whereas during astrocytogenesis Ascl1 functions in balancing the number of dorsal GM protoplasmic astrocytes with dorsal WM fibrous astrocytes. Thus, in addition to its function in neurogenesis, Ascl1 marks glial progenitors and controls the number and distribution of astrocytes and oligodendrocytes in the GM and WM of the spinal cord.

Citing Articles

An integrative analysis of ASCL1 in breast cancer and inhibition of ASCL1 increases paclitaxel sensitivity by activating ferroptosis via the CREB1/GPX4 axis.

Yang X, Li Y, Peng Y, Chang Y, He B, Zhang T Front Immunol. 2025; 16:1546794.

PMID: 39963143 PMC: 11830715. DOI: 10.3389/fimmu.2025.1546794.


Transcription factors ASCL1 and OLIG2 drive glioblastoma initiation and co-regulate tumor cell types and migration.

Myers B, Brayer K, Paez-Beltran L, Villicana E, Keith M, Suzuki H Nat Commun. 2024; 15(1):10363.

PMID: 39609428 PMC: 11605073. DOI: 10.1038/s41467-024-54750-9.


A conserved molecular logic for neurogenesis to gliogenesis switch in the cerebral cortex.

Liang X, Hoang K, Meyerink B, Kc P, Paraiso K, Wang L Proc Natl Acad Sci U S A. 2024; 121(20):e2321711121.

PMID: 38713624 PMC: 11098099. DOI: 10.1073/pnas.2321711121.


Excitatory Spinal Lhx9-Derived Interneurons Modulate Locomotor Frequency in Mice.

Bertho M, Caldeira V, Hsu L, Low P, Borgius L, Kiehn O J Neurosci. 2024; 44(18).

PMID: 38438260 PMC: 11063822. DOI: 10.1523/JNEUROSCI.1607-23.2024.


Context-dependent regulation of Notch signaling in glial development and tumorigenesis.

Guo R, Han D, Song X, Gao Y, Li Z, Li X Sci Adv. 2023; 9(45):eadi2167.

PMID: 37948517 PMC: 10637744. DOI: 10.1126/sciadv.adi2167.


References
1.
Hoffmann S, Hos D, Kuspert M, Lang R, Lovell-Badge R, Wegner M . Stem cell factor Sox2 and its close relative Sox3 have differentiation functions in oligodendrocytes. Development. 2013; 141(1):39-50. PMC: 3865748. DOI: 10.1242/dev.098418. View

2.
Wildner H, Muller T, Cho S, Brohl D, Cepko C, Guillemot F . dILA neurons in the dorsal spinal cord are the product of terminal and non-terminal asymmetric progenitor cell divisions, and require Mash1 for their development. Development. 2006; 133(11):2105-13. DOI: 10.1242/dev.02345. View

3.
Nishiyama A, Komitova M, Suzuki R, Zhu X . Polydendrocytes (NG2 cells): multifunctional cells with lineage plasticity. Nat Rev Neurosci. 2008; 10(1):9-22. DOI: 10.1038/nrn2495. View

4.
Parras C, Galli R, Britz O, Soares S, Galichet C, Battiste J . Mash1 specifies neurons and oligodendrocytes in the postnatal brain. EMBO J. 2004; 23(22):4495-505. PMC: 526464. DOI: 10.1038/sj.emboj.7600447. View

5.
Walther E, Dichgans M, Maricich S, Romito R, Yang F, Dziennis S . Genomic sequences of aldolase C (Zebrin II) direct lacZ expression exclusively in non-neuronal cells of transgenic mice. Proc Natl Acad Sci U S A. 1998; 95(5):2615-20. PMC: 19434. DOI: 10.1073/pnas.95.5.2615. View