Evidence map›Paper›PMID 28578316›Full record

ArticleThe Journal of biological chemistry2017

Docosahexaenoic acid preserves visual function by maintaining correct disc morphology in retinal photoreceptor cells.

Hideo Shindou, Hideto Koso, Junko Sasaki, Hiroki Nakanishi, Hiroshi Sagara, Koh M Nakagawa, Yoshikazu Takahashi, Daisuke Hishikawa, Yoshiko Iizuka-Hishikawa, Fuyuki Tokumasu and 4 more

Open access · hybridAbstract read
In one paragraph

Article in The Journal of biological chemistry, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 92 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
92citing papers in PubMed, 1 pooled it
5.1field-weighted citation impact, top 4% of its field
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

92 citing papers in PubMed, 1 synthesis or guideline pooled it, 164 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Polyunsaturated fatty acid metabolism in the retinal pigment epithelium and its association with outer retinal disease.Mammalian genome : official journal of the International Mammalian Genome Society · 2026
    Review
  4. Article
  5. Review
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  7. Ferroptosis: The Demise of Cells Through Phospholipid Peroxidation.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2026
    Review
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32 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

14 authors at 3 institutions in 2 countries.

Hideo ShindouDepartment of Lipid Signaling, National Center for Global Health and Medicine, Shinjuku-ku, Tokyo 162-8655; Department of Lipid Science, Graduate School of Medicine, University of Tokyo, Bunkyo-ku, Tokyo 113-0033; Agency for Medical Research and Development (AMED)-Core Research for Evolution Science and Technology (CREST), Chiyoda-ku, Tokyo 100-0004. Electronic address: hshindou-tky@umin.net.
Hideto KosoDivision of Molecular and Developmental Biology, Institute of Medical Science, University of Tokyo, Shirokanedai, Minato-ku, Tokyo 108-8639.
Junko SasakiDepartment of Medical Biology, Akita University Graduate School of Medicine, Akita 010-8543.
Hiroki NakanishiResearch Center for Biosignal, Akita University Graduate School of Medicine, Akita 010-8502; Akita Lipid Technologies, LLC, Akita 010-0825.
Hiroshi SagaraMedical Proteomics Laboratory, Institute of Medical Science, University of Tokyo, Shirokanedai, Minato-ku, Tokyo 108-8639.
Koh M NakagawaInstitute for Solid State Physics, University of Tokyo, Kashiwa, Chiba 277-8581, Japan.
Yoshikazu TakahashiDepartment of Lipid Signaling, National Center for Global Health and Medicine, Shinjuku-ku, Tokyo 162-8655.
Daisuke HishikawaDepartment of Lipid Signaling, National Center for Global Health and Medicine, Shinjuku-ku, Tokyo 162-8655.
Yoshiko Iizuka-HishikawaDepartment of Lipid Signaling, National Center for Global Health and Medicine, Shinjuku-ku, Tokyo 162-8655.
Fuyuki TokumasuDepartment of Lipidomics, Graduate School of Medicine, University of Tokyo, Bunkyo-ku, Tokyo 113-0033.
Hiroshi NoguchiInstitute for Solid State Physics, University of Tokyo, Kashiwa, Chiba 277-8581, Japan.
Sumiko WatanabeDivision of Molecular and Developmental Biology, Institute of Medical Science, University of Tokyo, Shirokanedai, Minato-ku, Tokyo 108-8639.
Takehiko SasakiAgency for Medical Research and Development (AMED)-Core Research for Evolution Science and Technology (CREST), Chiyoda-ku, Tokyo 100-0004; Department of Medical Biology, Akita University Graduate School of Medicine, Akita 010-8543; Research Center for Biosignal, Akita University Graduate School of Medicine, Akita 010-8502; Akita Lipid Technologies, LLC, Akita 010-0825.
Takao ShimizuDepartment of Lipid Signaling, National Center for Global Health and Medicine, Shinjuku-ku, Tokyo 162-8655; Department of Lipidomics, Graduate School of Medicine, University of Tokyo, Bunkyo-ku, Tokyo 113-0033.
The University of Tokyo · JPAkita University · JPNational Center for Global Health and Medicine · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Docosahexaenoic acid (DHA) has essential roles in photoreceptor cells in the retina and is therefore crucial to healthy vision. Although the influence of dietary DHA on visual acuity is well known and the retina has an abundance of DHA-containing phospholipids (PL-DHA), the mechanisms associated with DHA's effects on visual function are unknown. We previously identified lysophosphatidic acid acyltransferase 3 (LPAAT3) as a PL-DHA biosynthetic enzyme. Here, using comprehensive phospholipid analyses and imaging mass spectroscopy, we found that LPAAT3 is expressed in the inner segment of photoreceptor cells and that PL-DHA disappears from the outer segment in the LPAAT3-knock-out mice. Dynamic light-scattering analysis of liposomes and molecular dynamics simulations revealed that the physical characteristics of DHA reduced membrane-bending rigidity. Following loss of PL-DHA, LPAAT3-knock-out mice exhibited abnormalities in the retinal layers, such as incomplete elongation of the outer segment and decreased thickness of the outer nuclear layers and impaired visual function, as well as disordered disc morphology in photoreceptor cells. Our results indicate that PL-DHA contributes to visual function by maintaining the disc shape in photoreceptor cells and that this is a function of DHA in the retina. This study thus provides the reason why DHA is required for visual acuity and may help inform approaches for overcoming retinal disorders associated with DHA deficiency or dysfunction.

Indexed as

AcyltransferasesAnimalsBiomarkersCrosses, GeneticDocosahexaenoic AcidsElectroretinographyLiposomesMembrane FluidityMice, Inbred C57BLMice, KnockoutMicroscopy, Electron, TransmissionMolecular Dynamics SimulationMultimodal ImagingOptical ImagingPhospholipidsPhotoreceptor Cells, Vertebrate2-acylglycerophosphate acyltransferaseAcyltransferasesBiomarkersDocosahexaenoic AcidsLiposomesLpaat3 protein, mousePhospholipidsDHAglycerophospholipidLPAAT3lysophospholipid acyltransferasemembrane biophysicsmembrane lipidphospholipid turnoverretinal degeneration

Identifiers

PMID28578316
PMCPMC5519357
OpenAlexW2620565698

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LicenceCC BY
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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 OpenQuestion graph.