Developmental Maturation of the Cerebellar White Matter—an Instructive Environment for Cerebellar Inhibitory Interneurons

• Published in: Cerebellum (London, England) England), 2020-04, Vol.19 (2), p.286-308
• Main Authors: Groteklaes, Anne, Bönisch, Carina, Eiberger, Britta, Christ, Andrea, Schilling, Karl
• Format: Article
• Language: English
• Subjects: Biomedical and Life Sciences; Biomedicine; Cell migration; Cerebellum; Cortex; Critical period; Glial fibrillary acidic protein; Immunocytochemistry; Interneurons; Maturation; Microglial cells; Neurobiology; Neurology; Neurosciences; Original Paper; Pax2 protein; Substantia alba; Substantia grisea
• ISSN: 1473-4222; 1473-4230
• DOI: 10.1007/s12311-020-01111-z

In the developing cerebellum, the nascent white matter (WM) serves as an instructive niche for cerebellar cortical inhibitory interneurons. As their Pax2 expressing precursors transit the emerging WM, their laminar fate is programmed. The source(s) and nature of the signals involved remain unknown. Here, we used immunocytochemistry to follow the cellular maturation of the murine cerebellar WM during this critical period. During the first few days of postnatal development, when most Pax2 expressing cells are formed and many of them reach the cerebellar gray matter, only microglial cells can be identified in the territories through which Pax2 cells migrate. From p4 onward, cells expressing the oligodendrocytic or astrocyte markers, CNP-1, MBP or GFAP, started to appear in the nascent WM. Expression of macroglial markers increased with cerebellar differentiation, yet deep nuclei remained GFAP-negative at all ages. The progressive spread of maturing glia did not correlate with the exit of Pax2 cells from the WM, as indicated by the extensive mingling of these cells up to p15. Whereas sonic hedgehog-associated p75 NTR expression could be verified in granule cell precursors, postmitotic Pax2 cells are p75 NTR negative at all ages analyzed. Thus, if Pax2 cells, like their precursors, are sensitive to sonic hedgehog, this does not affect their expression of p75 NTR . Our findings document that subsequently generated sets of Pax2 expressing precursors of inhibitory cerebellar interneurons are confronted with a dynamically changing complement of cerebellar glia. The eventual identification of fate-defining pathways should profit from the covariation with glial maturation predicted by the present findings.