Evidence map›Paper›PMID 40952938›Full record

ArticleDevelopmental neuroscience2026

Metabolic Reprogramming of Oligodendrocytes in Intrauterine Growth Restriction.

Hannah Peters, Camille M Fung, Robert W Dettman, Maria L V Dizon, Jill Chang

Abstract read
In one paragraph

Article in Developmental neuroscience, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

5 authors.

Hannah PetersDepartment of Pediatrics, Section of Neonatology, University of Colorado Anschutz Medical Campus, Aurora, Colorado, USA.
Camille M FungDepartment of Pediatrics, University of Utah, Salt Lake City, Utah, USA.
Robert W DettmanDivision of Neonatology, Department of Pediatrics, Ann and Robert H. Lurie Children's Hospital of Chicago, Chicago, Illinois, USA.
Maria L V DizonDivision of Neonatology, Department of Pediatrics, Ann and Robert H. Lurie Children's Hospital of Chicago, Chicago, Illinois, USA.
Jill ChangDepartment of Pediatrics, Section of Neonatology, University of Colorado Anschutz Medical Campus, Aurora, Colorado, USA, jill.chang@cuanschutz.edu.

Funding

PILOT STUDY--SUBSTRATE METABOLISM IN EXTREMELY LOW BIRTH WEIGHT INFANTSP30DK048520 · NIDDK · UNIVERSITY OF COLORADO DENVER · PI JANINE A HIGGINS · 1995 to 2026
$32.6M
Corticospinal Tract Development in Intrauterine Growth RestrictionK08HD102023 · NICHD · UNIVERSITY OF COLORADO DENVER · PI CHANG, JILL · 2020 to 2024
$811k
NICHD NIH HHS K08 HD102023NIDDK NIH HHS P30 DK048520
6 · The paper itself

Abstract

introductionIntrauterine growth restriction (IUGR) has been shown to adversely affect developing white matter, putting infants at risk for neurodevelopmental disability, including cerebral palsy. White matter injury (WMI) has been well documented in both human and animal studies of IUGR with sexual dimorphism. Currently, the underlying cellular mechanisms leading to WMI in IUGR remain poorly understood, but energy failure is a likely candidate.

methodsTo address these gaps, we evaluated for sex-specific changes to oligodendrocyte (OL) differentiation and the OL transcriptome, leveraging cell-specific epitope tagging and RNA isolation in a placental insufficiency-induced IUGR mouse model. OL mitochondrial respiration was further evaluated using primary cell isolation and Agilent Seahorse technology.

resultsWe found an early sex-specific arrest of OL differentiation in IUGR females, which was followed by late catch-up differentiation and proliferation. Cell-specific RNA sequencing demonstrated downregulation of genes involved in oxidative phosphorylation (OXPHOS) in IUGR. IUGR males demonstrated a greater downregulation of electron transport chain (ETC) genes and proteins than their IUGR female counterparts. Quantification of O4+ OL mitochondrial respiration also demonstrated decreased ATP generation in IUGR males via OXPHOS that was consistent with ETC gene and protein expression findings.

conclusionOur findings demonstrate sex-specific differences in OL differentiation and in mitochondrial metabolism in IUGR. These results provide insight into the different neurodevelopmental outcomes seen between IUGR males and females. These results also lay the foundation for investigation into targeted nutritional and pharmacologic management.

Indexed as

Fetal Growth RetardationOligodendrogliaAnimalsCell DifferentiationFemaleMaleMetabolic ReprogrammingMiceMice, Inbred C57BLMitochondriaOxidative PhosphorylationPregnancyIntrauterine growth restrictionOligodendrocyteOxidative phosphorylationWhite matter injury

Identifiers

PMID40952938
PMCPMC12505750

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.