Novel role of Rac-Mid1 signaling in medial cerebellar development

T Nakamura, T Ueyama, Y Ninoyu, H Sakaguchi, N Choijookhuu, Y Hishikawa, H Kiyonari, M Kohta, M Sakahara, I de Curtis, E Kohmura, Y Hisa, A Aiba, N Saito

Research output: Contribution to journalArticlepeer-review

Abstract

Rac signaling impacts a relatively large number of downstream targets; however, few studies have established an association between Rac pathways and pathological conditions. In the present study, we generated mice with double knockout of Rac1 and Rac3 (Atoh1-Cre;Rac1flox/flox;Rac3−/−) in cerebellar granule neurons (CGNs). We observed impaired tangential migration at E16.5, as well as numerous apoptotic CGNs at the deepest layer of the external granule layer (EGL) in the medial cerebellum of Atoh1-Cre; Rac1flox/flox;Rac3−/− mice at P8. Atoh1-Cre;Rac1flox/flox;Rac3−/− CGNs differentiated normally until expression of p27kip1 and NeuN in the deep EGL at P5. Primary CGNs and cerebellar microexplants from Atoh1-Cre;Rac1flox/flox;Rac3−/− mice exhibited impaired neuritogenesis, which was more apparent in Map2-positive dendrites. Such findings suggest that impaired tangential migration and final differentiation of CGNs have resulted in decreased cerebellum size and agenesis of the medial internal granule layer, respectively. Furthermore, Rac depleted/deleted cells exhibited decreased levels of Mid1 and impaired mTORC1 signaling. Mid1 depletion in CGNs produced mild impairments in neuritogenesis and reductions in mTORC1 signaling. Thus, a novel Rac-signaling pathway (Rac1-Mid1-mTORC1) may be involved in medial cerebellar development. © 2017. Published by The Company of Biologists Ltd.
Original languageEnglish
Pages (from-to)1863-1875
Number of pages13
JournalDevelopment (Cambridge)
Volume144
Issue number10
DOIs
Publication statusPublished - 2017

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