Evidence map›Paper›PMID 40498764›Full record

ArticlePloS one2025

Drosophila models uncover substrate channeling effects on phospholipids and sphingolipids in peroxisomal biogenesis disorders.

Michael F Wangler, Yu-Hsin Chao, Mary Roth, Ruth Welti, James A McNew

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In one paragraph

Article in PloS one, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

4 citing papers in PubMed.

  1. Article
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

5 authors.

Michael F WanglerMolecular and Human Genetics, Baylor College of Medicine, Houston, Texas, United States of America.ORCID https://orcid.org/0000-0001-5245-5910
Yu-Hsin ChaoMolecular and Human Genetics, Baylor College of Medicine, Houston, Texas, United States of America.
Mary RothKansas Lipidomics Research Center, Division of Biology, Kansas State University, Manhattan, Kansas, United States of America.
Ruth WeltiKansas Lipidomics Research Center, Division of Biology, Kansas State University, Manhattan, Kansas, United States of America.
James A McNewDepartment of BIoSciences, Rice University, Houston, Texas, United States of America.ORCID https://orcid.org/0000-0001-8459-3664

Funding

Mentoring CoreP20GM103418 · NIGMS · UNIVERSITY OF KANSAS MEDICAL CENTER · PI Douglas E Wright · 2012 to 2026
$63.0M
Neuronal Mechanisms of Metabolic and Genetic Defects of the PeroxisomeR01NS107733 · NINDS · BAYLOR COLLEGE OF MEDICINE · PI WANGLER, MICHAEL FRANCIS · 2021 to 2025
$2.3M
NIGMS NIH HHS P20 GM103418NINDS NIH HHS R01 NS107733
6 · The paper itself

Abstract

Peroxisomal Biogenesis Disorders Zellweger Spectrum (PBD-ZSD) disorders are a group of autosomal recessive defects in peroxisome formation that produce a multi-systemic disease presenting at birth or in childhood. Well documented clinical biomarkers such as elevated very long chain fatty acids (VLCFA) are key biochemical diagnostic findings in these conditions. Additional, secondary biochemical alterations such as elevated very long chain lysophosphatidylcholines are allowing newborn screening for peroxisomal disease. In addition, a more widespread impact on metabolism and lipids is increasingly being documented by metabolomic and lipidomic studies. Here we utilize Drosophila models of pex2 and pex16 as well as human plasma from individuals with PEX1 mutations. We identify phospholipid abnormalities in Drosophila larvae and brain characterized by differences in the quantities of phosphatidylcholine (PC) and phosphatidylethanolamines (PE) with long chain lengths and reduced levels of intermediate chain lengths. For diacylglycerol (DAG), the precursor of PE and PC through the Kennedy pathway, the intermediate chain lengths are increased suggesting an imbalance between DAGs and PE and PC that suggests the two acyl chain pools are not in equilibrium. Altered acyl chain lengths are also observed in PE ceramides in the fly models. Interestingly, plasma from human subjects exhibit phospholipid alterations similar to the fly model. Moreover, human plasma shows reduced levels of sphingomyelin with 18 and 22 carbon lengths but normal levels of C24. Our results suggest that peroxisomal biogenesis defects alter shuttling of the acyl chains of multiple phospholipid and ceramide lipid classes. In contrast, DAG species with intermediate fatty acids are actually more abundant in PBD. These data suggest an imbalance between de novo synthesis of PC and PE through the Kennedy pathway and remodeling of existing PC and PE through the Lands cycle. This imbalance is likely due to overabundance of very long acyl chains in PBD and a subsequent imbalance due to substrate channeling effects. Given the fundamental role of phospholipid and sphingolipids in nervous system functions, these observations suggest PBD-ZSD are diseases characterized by widespread cell membrane lipid abnormalities.

Indexed as

Peroxisomal DisordersPhospholipidsSphingolipidsAnimalsATPases Associated with Diverse Cellular ActivitiesDisease Models, AnimalDrosophilaDrosophila melanogasterDrosophila ProteinsHumansMembrane ProteinsMutationPeroxinsPeroxisomal Targeting Signal 2 ReceptorPeroxisomesZellweger SyndromeATPases Associated with Diverse Cellular ActivitiesDrosophila ProteinsMembrane ProteinsPeroxinsPeroxisomal Targeting Signal 2 ReceptorPEX1 protein, humanPhospholipidsSphingolipids

Identifiers

PMID40498764
PMCPMC12157166

What Socratic holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

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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 Socratic graph.