4.8 Article

Quantitative Lipidomics and Spatial MS-Imaging Uncovered Neurological and Systemic Lipid Metabolic Pathways Underlying Troglomorphic Adaptations in Cave-Dwelling Fish

Journal

MOLECULAR BIOLOGY AND EVOLUTION
Volume 39, Issue 4, Pages -

Publisher

OXFORD UNIV PRESS
DOI: 10.1093/molbev/msac050

Keywords

lipidomics; mass-spectrometry imaging; cavefish; lipid metabolism; docosahexaenoic acid; arachidonic acid; oxidative phosphorylation

Funding

  1. National Natural Science Foundation of China [NSFC92057202, NSFC31872218]
  2. National Key R&D Program of China [2018YFA0506900, 2018YFA0800901, 2019YFA0802402]

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The neural compartmentalization of lipid distribution and metabolism is associated with troglomorphic traits in Sinocyclocheilus cavefish. This includes reductions in DHA-phospholipids and accumulation of arachidonic acid-phospholipids in the brain, demyelination in serotonergic neurons, and systemic reductions in esterified DHAs in the liver. These adaptations serve to reduce energy expenditure and are crucial for the survival of cavefish in cave environments.
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 Delta 4 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 beta-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.

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