Characterization of sciatic nerve myelin sheath during development in C57BL/6 mice

Author:

Chen Yuhan1,Shang Tongxin1,Sun Junjie1,Ji Yuhua1,Gong Leilei12,Li Aihong3,Ding Fei1,Shen Mi1,Zhang Qi1

Affiliation:

1. Key Laboratory of Neuroregeneration of Jiangsu and Ministry of Education, Medical School, Co‐innovation Center of Neuroregeneration, NMPA Key Laboratory for Research and Evaluation of Tissue Engineering Technology Products, Jiangsu Clinical Medicine Center of Tissue Engineering and Nerve Injury Repair Nantong University Nantong China

2. Research and Development Center for E‐Learning Ministry of Education Beijing China

3. Department of Neurology, Affiliated Hospital of Nantong University, Medical School Nantong University Nantong China

Abstract

AbstractMyelin sheath plays important roles in information conduction and nerve injury repair in the peripheral nerve system (PNS). Enhancing comprehension of the structure and components of the myelin sheath in the PNS during development would contribute to a more comprehensive understanding of the developmental and regenerative processes. In this research, the structure of sciatic nerve myelin sheath in C57BL/6 mice from embryonic day 14 (E14) to postnatal 12 months (12M) was observed with transmission electron microscopy. Myelin structure appeared in the sciatic nerve as early as E14, and the number and thickness of myelin lamellar gradually increased with the development until 12M. Transcriptome analysis was performed to show the expressions of myelin‐associated genes and transcriptional factors involved in myelin formation. The genes encoding myelin proteins (Mag, Pmp22, Mpz, Mbp, Cnp and Prx) showed the same expression pattern, peaking at postnatal day 7 (P7) and P28 after birth, whereas the negative regulators of myelination (c‐Jun, Tgfb1, Tnc, Cyr61, Ngf, Egr1, Hgf and Bcl11a) showed an opposite expression pattern. In addition, the expression of myelin‐associated proteins and transcriptional factors was measured by Western blot and immunofluorescence staining. The protein expressions of MAG, PMP22, MPZ, CNPase and PRX increased from E20 to P14. The key transcriptional factor c‐Jun co‐localized with the Schwann cells Marker S100β and decreased after birth, whereas Krox20/Egr2 increased during development. Our data characterized the structure and components of myelin sheath during the early developmental stages, providing insights for further understanding of PNS development.

Funder

National Natural Science Foundation of China

Nantong University

Priority Academic Program Development of Jiangsu Higher Education Institutions

Publisher

Wiley

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