» Articles » PMID: 38256095

Comparative Transcriptomic Analysis of Cerebellar Astrocytes Across Developmental Stages and Brain Regions

Overview
Journal Int J Mol Sci
Publisher MDPI
Date 2024 Jan 23
PMID 38256095
Authors
Affiliations
Soon will be listed here.
Abstract

Astrocytes are the most abundant glial cell type in the central nervous system, and they play a crucial role in normal brain function. While gliogenesis and glial differentiation occur during perinatal cerebellar development, the processes that occur during early postnatal development remain obscure. In this study, we conducted transcriptomic profiling of postnatal cerebellar astrocytes at postnatal days 1, 7, 14, and 28 (P1, P7, P14, and P28), identifying temporal-specific gene signatures at each specific time point. Comparing these profiles with region-specific astrocyte differentially expressed genes (DEGs) published for the cortex, hippocampus, and olfactory bulb revealed cerebellar-specific gene signature across these developmental timepoints. Moreover, we conducted a comparative analysis of cerebellar astrocyte gene signatures with gene lists from pediatric brain tumors of cerebellar origin, including ependymoma and medulloblastoma. Notably, genes downregulated at P14, such as Kif11 and HMGB2, exhibited significant enrichment across all pediatric brain tumor groups, suggesting the importance of astrocytic gene repression during cerebellar development to these tumor subtypes. Collectively, our studies describe gene expression patterns during cerebellar astrocyte development, with potential implications for pediatric tumors originating in the cerebellum.

Citing Articles

Alzheimer's Disease, Obesity, and Type 2 Diabetes: Focus on Common Neuroglial Dysfunctions (Critical Review and New Data on Human Brain and Models).

Toledano A, Rodriguez-Casado A, Alvarez M, Toledano-Diaz A Brain Sci. 2024; 14(11).

PMID: 39595866 PMC: 11591712. DOI: 10.3390/brainsci14111101.

References
1.
Taylor M, Poppleton H, Fuller C, Su X, Liu Y, Jensen P . Radial glia cells are candidate stem cells of ependymoma. Cancer Cell. 2005; 8(4):323-35. DOI: 10.1016/j.ccr.2005.09.001. View

2.
Endo F, Kasai A, Soto J, Yu X, Qu Z, Hashimoto H . Molecular basis of astrocyte diversity and morphology across the CNS in health and disease. Science. 2022; 378(6619):eadc9020. PMC: 9873482. DOI: 10.1126/science.adc9020. View

3.
Love M, Huber W, Anders S . Moderated estimation of fold change and dispersion for RNA-seq data with DESeq2. Genome Biol. 2014; 15(12):550. PMC: 4302049. DOI: 10.1186/s13059-014-0550-8. View

4.
Haldipur P, Millen K, Aldinger K . Human Cerebellar Development and Transcriptomics: Implications for Neurodevelopmental Disorders. Annu Rev Neurosci. 2022; 45:515-531. PMC: 9271632. DOI: 10.1146/annurev-neuro-111020-091953. View

5.
Lin C, Yu K, Hatcher A, Huang T, Lee H, Carlson J . Identification of diverse astrocyte populations and their malignant analogs. Nat Neurosci. 2017; 20(3):396-405. PMC: 5824716. DOI: 10.1038/nn.4493. View