The Fragile X Messenger Ribonucleoprotein 1 Regulates the Morphology and Maturation of Human and Rat Oligodendrocytes

The Fragile X Messenger Ribonucleoprotein (FMRP) is an RNA binding protein that regulates the translation of multiple mRNAs and is expressed by neurons and glia in the mammalian brain. Loss of FMRP leads to fragile X syndrome (FXS), a common inherited form of intellectual disability and autism. While most research has been focusing on the neuronal contribution to FXS pathophysiology, the role of glia, particularly oligodendrocytes, is largely unknown. FXS individuals are characterized by white matter changes, which imply impairments in oligodendrocyte differentiation and myelination. We hypothesized that FMRP regulates oligodendrocyte maturation and myelination during postnatal development. Using a combination of human pluripotent stem cell-derived oligodendrocytes and an Fmr1 knockout rat model, we studied the role of FMRP on mammalian oligodendrocyte development. We found that the loss of FMRP leads to shared defects in oligodendrocyte morphology in both rat and human systems in vitro, which persist in the presence of FMRP-expressing axons in chimeric engraftment models. Our findings point to species-conserved, cell-autonomous defects during oligodendrocyte maturation in FXS.

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Journal
Glia
Published
2025-02-10
DOI
https://doi.org/10.1002/glia.24680
Citations
2
Primary Topic
Genetics and Neurodevelopmental Disorders
Type
article
Field-Weighted Citation Impact
3.63

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article

The Fragile X Messenger Ribonucleoprotein 1 Regulates the Morphology and Maturation of Human and Rat Oligodendrocytes

Sumantra Chattarji, Peter C. Kind, David Story, Vidya Ramesh et al.
2 citations
Glia
Genetics and Neurodevelopmental Disorders
3.63
article

The Fragile X Messenger Ribonucleoprotein 1 Regulates the Morphology and Maturation of Human and Rat Oligodendrocytes

Sumantra Chattarji, Peter C. Kind, David Story, Vidya Ramesh, Owen Robert Dando, Bhuvaneish Thangaraj Selvaraj, Lida Zoupi, Eleni Tsoukala, Biju Viswanath, Siddharthan Chandran, David W. Hampton, Zrinko Kozić, K. R. Bharath Kumar Reddy, Rakhi Pal, Ioanna Kougianou, Karen Burr
article en
2 citations

Abstract

The Fragile X Messenger Ribonucleoprotein (FMRP) is an RNA binding protein that regulates the translation of multiple mRNAs and is expressed by neurons and glia in the mammalian brain. Loss of FMRP leads to fragile X syndrome (FXS), a common inherited form of intellectual disability and autism. While most research has been focusing on the neuronal contribution to FXS pathophysiology, the role of glia, particularly oligodendrocytes, is largely unknown. FXS individuals are characterized by white matter changes, which imply impairments in oligodendrocyte differentiation and myelination. We hypothesized that FMRP regulates oligodendrocyte maturation and myelination during postnatal development. Using a combination of human pluripotent stem cell-derived oligodendrocytes and an Fmr1 knockout rat model, we studied the role of FMRP on mammalian oligodendrocyte development. We found that the loss of FMRP leads to shared defects in oligodendrocyte morphology in both rat and human systems in vitro, which persist in the presence of FMRP-expressing axons in chimeric engraftment models. Our findings point to species-conserved, cell-autonomous defects during oligodendrocyte maturation in FXS.

GliaVol. 73(6)
Tata Institute of Fundamental Research (IN), National Centre for Biological Sciences (IN), Institute for Stem Cell Biology and Regenerative Medicine (IN), MRC Centre for Regenerative Medicine (GB), UK Dementia Research Institute (GB), National Institute of Mental Health and Neurosciences (IN), University of Edinburgh (GB)
Wellcome Trust, University of Edinburgh, Department of Biotechnology, Ministry of Science and Technology, India, The Wellcome Trust DBT India Alliance, Simons Initiative for the Developing Brain, UK Dementia Research Institute, Medical Research Council, Biotechnology and Biological Sciences Research Council, National Centre for Biological Sciences
Openalex Percentile: Top 9%
Genetics and Neurodevelopmental Disorders
3.63
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