Bcl2l12, a novel protein interacting with Arf6, triggers Schwann cell differentiation programme

Schwann cells are glial cells in the peripheral nervous system (PNS); they wrap neuronal axons with their differentiated plasma membranes called myelin sheaths. Although the physiological functions, such as generating saltatory conduction, have been well studied in the PNS, the molecular mechanisms by which Schwann cells undergo their differentiation programme without apparent morphological changes before dynamic myelin sheath formation remain unclear. Here, for the first time, we report that Arf6, a small GTP/GDP-binding protein controlling morphological differentiation, and the guanine-nucleotide exchange factors cytohesin proteins are involved in the regulation of Schwann cell differentiation marker expression in primary Schwann cells. Specific inhibition of Arf6 and cytohesins by NAV-2729 and SecinH3, respectively, decreased expression of marker proteins 2',3'-cyclic nucleotide 3'-phosphodiesterase (CNPase) and glial fibrillary acidic protein (GFAP). Similar results using promoter assays were observed using the IMS32 Schwann cell line. Furthermore, using an affinity-precipitation technique, we identified Bcl2-like 12 (Bcl2l12) as a novel GTP-bound Arf6-interacting protein. Knockdown of Bcl2l12 using a specific artificial miRNA decreased expression of marker proteins. The knockdown also led to decreased filamentous actin extents. These results suggest that Arf6 and Bcl2l12 can trigger Schwann cell differentiation, providing evidence for a molecular relay that underlies how Schwann cells differentiate.

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Publication Details

Journal
The Journal of Biochemistry
Published
2024-11-06
DOI
https://doi.org/10.1093/jb/mvae078
Primary Topic
Neuroblastoma Research and Treatments
Type
article
Field-Weighted Citation Impact
0.00

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article

Bcl2l12, a novel protein interacting with Arf6, triggers Schwann cell differentiation programme

Wakana Miyata, Hideji Yako, Kentaro Yoshinaga, Junji Yamauchi et al.
The Journal of Biochemistry
Neuroblastoma Research and Treatments
article

Bcl2l12, a novel protein interacting with Arf6, triggers Schwann cell differentiation programme

Wakana Miyata, Hideji Yako, Kentaro Yoshinaga, Junji Yamauchi, Yuki Miyamoto, Asahi Honjo, Kazunori Sango, Mikito Takahashi, Naoko Sakaibara, Tatsuya Ooki
article en

Abstract

Schwann cells are glial cells in the peripheral nervous system (PNS); they wrap neuronal axons with their differentiated plasma membranes called myelin sheaths. Although the physiological functions, such as generating saltatory conduction, have been well studied in the PNS, the molecular mechanisms by which Schwann cells undergo their differentiation programme without apparent morphological changes before dynamic myelin sheath formation remain unclear. Here, for the first time, we report that Arf6, a small GTP/GDP-binding protein controlling morphological differentiation, and the guanine-nucleotide exchange factors cytohesin proteins are involved in the regulation of Schwann cell differentiation marker expression in primary Schwann cells. Specific inhibition of Arf6 and cytohesins by NAV-2729 and SecinH3, respectively, decreased expression of marker proteins 2',3'-cyclic nucleotide 3'-phosphodiesterase (CNPase) and glial fibrillary acidic protein (GFAP). Similar results using promoter assays were observed using the IMS32 Schwann cell line. Furthermore, using an affinity-precipitation technique, we identified Bcl2-like 12 (Bcl2l12) as a novel GTP-bound Arf6-interacting protein. Knockdown of Bcl2l12 using a specific artificial miRNA decreased expression of marker proteins. The knockdown also led to decreased filamentous actin extents. These results suggest that Arf6 and Bcl2l12 can trigger Schwann cell differentiation, providing evidence for a molecular relay that underlies how Schwann cells differentiate.

The Journal of BiochemistryVol. 177(1)
Tokyo University of Pharmacy and Life Sciences (JP), Tokyo Metropolitan Institute of Medical Science (JP), National Center For Child Health and Development (JP)
Ministry of Education, Culture, Sports, Science and Technology, Core Research for Evolutional Science and Technology
Decent work and economic growth
Openalex Percentile: Top 69%
Neuroblastoma Research and Treatments
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