Long chain acyl‐CoA synthetase 6 facilitates the local distribution of di‐docosahexaenoic acid‐ and ultra‐long‐chain‐PUFA‐containing phospholipids in the retina to support normal visual function in mice

Docosahexaenoic acid (DHA) and ultra‐long‐chain polyunsaturated fatty acids (ULC–PUFAs) are uniquely enriched in membrane phospholipids of retinal photoreceptors. Several studies have shown that di‐DHA‐ and ULC–PUFA‐containing phospholipids in photoreceptors have an important role in maintaining nor...

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Veröffentlicht in:The FASEB journal 2023-09, Vol.37 (9), p.e23151-n/a
Hauptverfasser: Kuroha, Sayoko, Katada, Yusaku, Isobe, Yosuke, Uchino, Haruki, Shishikura, Kyosuke, Nirasawa, Takashi, Tsubota, Kazuo, Negishi, Kazuno, Kurihara, Toshihide, Arita, Makoto
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container_issue 9
container_start_page e23151
container_title The FASEB journal
container_volume 37
creator Kuroha, Sayoko
Katada, Yusaku
Isobe, Yosuke
Uchino, Haruki
Shishikura, Kyosuke
Nirasawa, Takashi
Tsubota, Kazuo
Negishi, Kazuno
Kurihara, Toshihide
Arita, Makoto
description Docosahexaenoic acid (DHA) and ultra‐long‐chain polyunsaturated fatty acids (ULC–PUFAs) are uniquely enriched in membrane phospholipids of retinal photoreceptors. Several studies have shown that di‐DHA‐ and ULC–PUFA‐containing phospholipids in photoreceptors have an important role in maintaining normal visual function; however, the molecular mechanisms underlying the synthesis and enrichment of these unique lipids in the retina, and their specific roles in retinal function remain unclear. Long‐chain acyl‐coenzyme A (CoA) synthetase 6 (ACSL6) preferentially converts DHA into DHA–CoA, which is a substrate during DHA‐containing lipid biosynthesis. Here, we report that Acsl6 mRNA is expressed in the inner segment of photoreceptor cells and the retinal pigment epithelial cells, and genetic deletion of ACSL6 resulted in the selective depletion of di‐DHA– and ULC–PUFA‐containing phospholipids, but not mono‐DHA‐containing phospholipids in the retina. MALDI mass spectrometry imaging (MALDI–MSI) revealed the selective distribution of di‐DHA– and ULC–PUFA‐containing phospholipids in the photoreceptor outer segment (OS). Electroretinogram of Acsl6−/− mice exhibited photoreceptor cell‐derived visual impairment, whereas the expression levels and localization of opsin proteins were unchanged. Acsl6−/− mice exhibited an age‐dependent progressive decrease of the thickness of the outer nuclear layers, whereas the inner nuclear layers and OSs were normal. These results demonstrate that ACSL6 facilitates the local enrichment of di‐DHA– and ULC–PUFA‐containing phospholipids in the retina, which supports normal visual function and retinal homeostasis. Di‐DHA‐ and ULC‐PUFA‐containing phospholipids in the OS disk membrane layer of the retina were decreased in ACSL6‐deficient mice. ACSL6‐deficient mice developed impaired photoreceptor‐derived visual function and age‐dependent retinal degeneration. These results demonstrate that ACSL6 facilitates the local enrichment of di‐DHA‐ and ULC‐PUFA‐containing phospholipids in the retina, which supports normal visual function and retinal homeostasis. Image created with BioRender.
doi_str_mv 10.1096/fj.202300976R
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Electroretinogram of Acsl6−/− mice exhibited photoreceptor cell‐derived visual impairment, whereas the expression levels and localization of opsin proteins were unchanged. Acsl6−/− mice exhibited an age‐dependent progressive decrease of the thickness of the outer nuclear layers, whereas the inner nuclear layers and OSs were normal. These results demonstrate that ACSL6 facilitates the local enrichment of di‐DHA– and ULC–PUFA‐containing phospholipids in the retina, which supports normal visual function and retinal homeostasis. Di‐DHA‐ and ULC‐PUFA‐containing phospholipids in the OS disk membrane layer of the retina were decreased in ACSL6‐deficient mice. ACSL6‐deficient mice developed impaired photoreceptor‐derived visual function and age‐dependent retinal degeneration. These results demonstrate that ACSL6 facilitates the local enrichment of di‐DHA‐ and ULC‐PUFA‐containing phospholipids in the retina, which supports normal visual function and retinal homeostasis. 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Several studies have shown that di‐DHA‐ and ULC–PUFA‐containing phospholipids in photoreceptors have an important role in maintaining normal visual function; however, the molecular mechanisms underlying the synthesis and enrichment of these unique lipids in the retina, and their specific roles in retinal function remain unclear. Long‐chain acyl‐coenzyme A (CoA) synthetase 6 (ACSL6) preferentially converts DHA into DHA–CoA, which is a substrate during DHA‐containing lipid biosynthesis. Here, we report that Acsl6 mRNA is expressed in the inner segment of photoreceptor cells and the retinal pigment epithelial cells, and genetic deletion of ACSL6 resulted in the selective depletion of di‐DHA– and ULC–PUFA‐containing phospholipids, but not mono‐DHA‐containing phospholipids in the retina. MALDI mass spectrometry imaging (MALDI–MSI) revealed the selective distribution of di‐DHA– and ULC–PUFA‐containing phospholipids in the photoreceptor outer segment (OS). 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source Wiley Online Library Journals Frontfile Complete; Alma/SFX Local Collection
subjects docosahexaenoic acid
lipidomics
long‐chain acyl‐coenzyme a (CoA) synthetase 6
photoreceptor cells
ultra‐long‐chain polyunsaturated fatty acid
title Long chain acyl‐CoA synthetase 6 facilitates the local distribution of di‐docosahexaenoic acid‐ and ultra‐long‐chain‐PUFA‐containing phospholipids in the retina to support normal visual function in mice
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