Molecular control of oligodendrocyte development

B Elbaz, B Popko - Trends in neurosciences, 2019 - cell.com
Myelin is a multilayer lipid membrane structure that wraps and insulates axons, allowing for
the efficient propagation of action potentials. During developmental myelination of the …

Using the lineage determinants Olig2 and Sox10 to explore transcriptional regulation of oligodendrocyte development

E Sock, M Wegner - Developmental neurobiology, 2021 - Wiley Online Library
The transcription factors Olig2 and Sox10 jointly define oligodendroglial identity. Because of
their continuous presence during development and in the differentiated state they shape the …

The Eph receptor A4 plays a role in demyelination and depression-related behavior

Y Li, P Su, Y Chen, J Nie, TF Yuan… - The Journal of …, 2022 - Am Soc Clin Investig
Proper myelination of axons is crucial for normal sensory, motor, and cognitive function.
Abnormal myelination is seen in brain disorders such as major depressive disorder (MDD) …

S100B is selectively expressed by gray matter protoplasmic astrocytes and myelinating oligodendrocytes in the developing CNS

J Du, M Yi, F Zhou, W He, A Yang, M Qiu, H Huang - Molecular Brain, 2021 - Springer
Studies on the development of central nervous system (CNS) primarily rely on the use of
specific molecular markers for different types of neural cells. S100B is widely being used as …

Central nervous system regeneration: the roles of glial cells in the potential molecular mechanism underlying remyelination

L Quan, A Uyeda, R Muramatsu - Inflammation and Regeneration, 2022 - Springer
Glial cells play crucial roles in brain homeostasis and pathogenesis of central nervous
system (CNS) injuries and diseases. However, the roles of these cells and the molecular …

Transcriptional control of myelination and remyelination

E Sock, M Wegner - Glia, 2019 - Wiley Online Library
Myelination is an evolutionary recent differentiation program that has been independently
acquired in vertebrates by Schwann cells in the peripheral nervous system and …

Variants in myelin regulatory factor (MYRF) cause autosomal dominant and syndromic nanophthalmos in humans and retinal degeneration in mice

SJ Garnai, ML Brinkmeier, B Emery, TS Aleman… - PLoS …, 2019 - journals.plos.org
Nanophthalmos is a rare, potentially devastating eye condition characterized by small eyes
with relatively normal anatomy, a high hyperopic refractive error, and frequent association …

The transcription factor NKX2-2 regulates oligodendrocyte differentiation through domain-specific interactions with transcriptional corepressors

C Zhang, H Huang, Z Chen, Z Zhang, W Lu… - Journal of Biological …, 2020 - ASBMB
The homeodomain protein NK2 homeobox 2 (NKX2-2) is a transcription factor that plays a
critical role in the control of cell fate specification and differentiation in many tissues. In the …

Detection of clinically relevant genetic variants in Chinese patients with nanophthalmos by trio-based whole-genome sequencing study

C Guo, Z Zhao, D Chen, S He, N Sun… - … & visual science, 2019 - iovs.arvojournals.org
Purpose: Nanophthalmos is a rare genetic disorder commonly characterized by a short axial
length (AL) and severe hyperopia. Mutations that have been identified through Mendelian …

A glance at the molecules that regulate oligodendrocyte myelination

S Wang, Y Wang, S Zou - Current Issues in Molecular Biology, 2022 - mdpi.com
Oligodendrocyte (OL) myelination is a critical process for the neuronal axon function in the
central nervous system. After demyelination occurs because of pathophysiology …