Cargando…
Quantitative Lipidomics and Spatial MS-Imaging Uncovered Neurological and Systemic Lipid Metabolic Pathways Underlying Troglomorphic Adaptations in Cave-Dwelling Fish
Sinocyclocheilus represents a rare, freshwater teleost genus endemic to China that comprises the river-dwelling surface fish and the cave-dwelling cavefish. Using a combinatorial approach of quantitative lipidomics and mass-spectrometry imaging (MSI), we demonstrated that neural compartmentalization...
Autores principales: | , , , , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2022
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9011034/ https://www.ncbi.nlm.nih.gov/pubmed/35277964 http://dx.doi.org/10.1093/molbev/msac050 |
_version_ | 1784687604817461248 |
---|---|
author | Lam, Sin Man Li, Jie Sun, Huan Mao, Weining Lu, Zongmin Zhao, Qingshuo Han, Chao Gong, Xia Jiang, Binhua Chua, Gek Huey Zhao, Zhenwen Meng, Fanwei Shui, Guanghou |
author_facet | Lam, Sin Man Li, Jie Sun, Huan Mao, Weining Lu, Zongmin Zhao, Qingshuo Han, Chao Gong, Xia Jiang, Binhua Chua, Gek Huey Zhao, Zhenwen Meng, Fanwei Shui, Guanghou |
author_sort | Lam, Sin Man |
collection | PubMed |
description | Sinocyclocheilus represents a rare, freshwater teleost genus endemic to China that comprises the river-dwelling surface fish and the cave-dwelling cavefish. Using a combinatorial approach of quantitative lipidomics and mass-spectrometry imaging (MSI), we demonstrated that neural compartmentalization of lipid distribution and lipid metabolism is associated with the evolution of troglomorphic traits in Sinocyclocheilus. Attenuated docosahexaenoic acid (DHA) biosynthesis via the Δ4 desaturase pathway led to reductions in DHA-phospholipids in cavefish cerebellum. Instead, cavefish accumulates arachidonic acid-phospholipids that may disfavor retinotectal arbor growth. Importantly, MSI of sulfatides coupled with immunostaining of myelin basic protein and transmission electron microscopy images of hindbrain axons revealed demyelination in cavefish raphe serotonergic neurons. Demyelination in cavefish parallels the loss of neuroplasticity governing social behavior such as aggressive dominance. Outside the brain, quantitative lipidomics and qRT-PCR revealed systemic reductions in membrane esterified DHAs in the liver, attributed to suppression of genes along the Sprecher pathway (elovl2, elovl5, and acox1). Development of fatty livers was observed in cavefish; likely mediated by an impeded mobilization of storage lipids, as evident in the diminished expressions of pnpla2, lipea, lipeb, dagla, and mgll; and suppressed β-oxidation of fatty acyls via both mitochondria and peroxisomes as reflected in the reduced expressions of cpt1ab, hadhaa, cpt2, decr1, and acox1. These neurological and systemic metabolic adaptations serve to reduce energy expenditure, forming the basis of recessive evolution that eliminates nonessential morphological and behavioral traits and giving cavefish a selective advantage to thrive in caves where proper resource allocation becomes a major determinant of survival. |
format | Online Article Text |
id | pubmed-9011034 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-90110342022-04-18 Quantitative Lipidomics and Spatial MS-Imaging Uncovered Neurological and Systemic Lipid Metabolic Pathways Underlying Troglomorphic Adaptations in Cave-Dwelling Fish Lam, Sin Man Li, Jie Sun, Huan Mao, Weining Lu, Zongmin Zhao, Qingshuo Han, Chao Gong, Xia Jiang, Binhua Chua, Gek Huey Zhao, Zhenwen Meng, Fanwei Shui, Guanghou Mol Biol Evol Discoveries Sinocyclocheilus represents a rare, freshwater teleost genus endemic to China that comprises the river-dwelling surface fish and the cave-dwelling cavefish. Using a combinatorial approach of quantitative lipidomics and mass-spectrometry imaging (MSI), we demonstrated that neural compartmentalization of lipid distribution and lipid metabolism is associated with the evolution of troglomorphic traits in Sinocyclocheilus. Attenuated docosahexaenoic acid (DHA) biosynthesis via the Δ4 desaturase pathway led to reductions in DHA-phospholipids in cavefish cerebellum. Instead, cavefish accumulates arachidonic acid-phospholipids that may disfavor retinotectal arbor growth. Importantly, MSI of sulfatides coupled with immunostaining of myelin basic protein and transmission electron microscopy images of hindbrain axons revealed demyelination in cavefish raphe serotonergic neurons. Demyelination in cavefish parallels the loss of neuroplasticity governing social behavior such as aggressive dominance. Outside the brain, quantitative lipidomics and qRT-PCR revealed systemic reductions in membrane esterified DHAs in the liver, attributed to suppression of genes along the Sprecher pathway (elovl2, elovl5, and acox1). Development of fatty livers was observed in cavefish; likely mediated by an impeded mobilization of storage lipids, as evident in the diminished expressions of pnpla2, lipea, lipeb, dagla, and mgll; and suppressed β-oxidation of fatty acyls via both mitochondria and peroxisomes as reflected in the reduced expressions of cpt1ab, hadhaa, cpt2, decr1, and acox1. These neurological and systemic metabolic adaptations serve to reduce energy expenditure, forming the basis of recessive evolution that eliminates nonessential morphological and behavioral traits and giving cavefish a selective advantage to thrive in caves where proper resource allocation becomes a major determinant of survival. Oxford University Press 2022-03-12 /pmc/articles/PMC9011034/ /pubmed/35277964 http://dx.doi.org/10.1093/molbev/msac050 Text en © The Author(s) 2022. Published by Oxford University Press on behalf of Society for Molecular Biology and Evolution. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Discoveries Lam, Sin Man Li, Jie Sun, Huan Mao, Weining Lu, Zongmin Zhao, Qingshuo Han, Chao Gong, Xia Jiang, Binhua Chua, Gek Huey Zhao, Zhenwen Meng, Fanwei Shui, Guanghou Quantitative Lipidomics and Spatial MS-Imaging Uncovered Neurological and Systemic Lipid Metabolic Pathways Underlying Troglomorphic Adaptations in Cave-Dwelling Fish |
title | Quantitative Lipidomics and Spatial MS-Imaging Uncovered Neurological and Systemic Lipid Metabolic Pathways Underlying Troglomorphic Adaptations in Cave-Dwelling Fish |
title_full | Quantitative Lipidomics and Spatial MS-Imaging Uncovered Neurological and Systemic Lipid Metabolic Pathways Underlying Troglomorphic Adaptations in Cave-Dwelling Fish |
title_fullStr | Quantitative Lipidomics and Spatial MS-Imaging Uncovered Neurological and Systemic Lipid Metabolic Pathways Underlying Troglomorphic Adaptations in Cave-Dwelling Fish |
title_full_unstemmed | Quantitative Lipidomics and Spatial MS-Imaging Uncovered Neurological and Systemic Lipid Metabolic Pathways Underlying Troglomorphic Adaptations in Cave-Dwelling Fish |
title_short | Quantitative Lipidomics and Spatial MS-Imaging Uncovered Neurological and Systemic Lipid Metabolic Pathways Underlying Troglomorphic Adaptations in Cave-Dwelling Fish |
title_sort | quantitative lipidomics and spatial ms-imaging uncovered neurological and systemic lipid metabolic pathways underlying troglomorphic adaptations in cave-dwelling fish |
topic | Discoveries |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9011034/ https://www.ncbi.nlm.nih.gov/pubmed/35277964 http://dx.doi.org/10.1093/molbev/msac050 |
work_keys_str_mv | AT lamsinman quantitativelipidomicsandspatialmsimaginguncoveredneurologicalandsystemiclipidmetabolicpathwaysunderlyingtroglomorphicadaptationsincavedwellingfish AT lijie quantitativelipidomicsandspatialmsimaginguncoveredneurologicalandsystemiclipidmetabolicpathwaysunderlyingtroglomorphicadaptationsincavedwellingfish AT sunhuan quantitativelipidomicsandspatialmsimaginguncoveredneurologicalandsystemiclipidmetabolicpathwaysunderlyingtroglomorphicadaptationsincavedwellingfish AT maoweining quantitativelipidomicsandspatialmsimaginguncoveredneurologicalandsystemiclipidmetabolicpathwaysunderlyingtroglomorphicadaptationsincavedwellingfish AT luzongmin quantitativelipidomicsandspatialmsimaginguncoveredneurologicalandsystemiclipidmetabolicpathwaysunderlyingtroglomorphicadaptationsincavedwellingfish AT zhaoqingshuo quantitativelipidomicsandspatialmsimaginguncoveredneurologicalandsystemiclipidmetabolicpathwaysunderlyingtroglomorphicadaptationsincavedwellingfish AT hanchao quantitativelipidomicsandspatialmsimaginguncoveredneurologicalandsystemiclipidmetabolicpathwaysunderlyingtroglomorphicadaptationsincavedwellingfish AT gongxia quantitativelipidomicsandspatialmsimaginguncoveredneurologicalandsystemiclipidmetabolicpathwaysunderlyingtroglomorphicadaptationsincavedwellingfish AT jiangbinhua quantitativelipidomicsandspatialmsimaginguncoveredneurologicalandsystemiclipidmetabolicpathwaysunderlyingtroglomorphicadaptationsincavedwellingfish AT chuagekhuey quantitativelipidomicsandspatialmsimaginguncoveredneurologicalandsystemiclipidmetabolicpathwaysunderlyingtroglomorphicadaptationsincavedwellingfish AT zhaozhenwen quantitativelipidomicsandspatialmsimaginguncoveredneurologicalandsystemiclipidmetabolicpathwaysunderlyingtroglomorphicadaptationsincavedwellingfish AT mengfanwei quantitativelipidomicsandspatialmsimaginguncoveredneurologicalandsystemiclipidmetabolicpathwaysunderlyingtroglomorphicadaptationsincavedwellingfish AT shuiguanghou quantitativelipidomicsandspatialmsimaginguncoveredneurologicalandsystemiclipidmetabolicpathwaysunderlyingtroglomorphicadaptationsincavedwellingfish |