Evidence map›Paper›PMID 42553286›Full record

ReviewFrontiers in cell and developmental biology2026

Lipid ciliology: specialized ciliary membrane lipids in physiology and disease.

Alamgir Hasan, Tomoka Morita, Moe Hirosawa, Nao Kitamura, Ryoya Murakami, Masamichi Mikuni, Daigo Kobayashi, Takeshi Itabashi, Tatsuo Miyamoto

Abstract readReview
In one paragraph

Review in Frontiers in cell and developmental biology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

9 authors.

Alamgir Hasan *Department of Cellular and Molecular Physiology, Graduate School of Medicine, Yamaguchi University, Ube, Yamaguchi, Japan.
Tomoka Morita *Department of Cellular and Molecular Physiology, Graduate School of Medicine, Yamaguchi University, Ube, Yamaguchi, Japan.
Moe HirosawaDepartment of Cellular and Molecular Physiology, Graduate School of Medicine, Yamaguchi University, Ube, Yamaguchi, Japan.
Nao KitamuraDivision of Advanced Genome Editing Therapy Research, Research Institute for Cell Design Medical Sciences, Yamaguchi University, Ube, Yamaguchi, Japan.
Ryoya MurakamiDepartment of Cellular and Molecular Physiology, Graduate School of Medicine, Yamaguchi University, Ube, Yamaguchi, Japan.
Masamichi MikuniDepartment of Cellular and Molecular Physiology, Graduate School of Medicine, Yamaguchi University, Ube, Yamaguchi, Japan.
Daigo KobayashiDepartment of Cellular and Molecular Physiology, Graduate School of Medicine, Yamaguchi University, Ube, Yamaguchi, Japan.
Takeshi ItabashiDepartment of Cellular and Molecular Physiology, Graduate School of Medicine, Yamaguchi University, Ube, Yamaguchi, Japan.
Tatsuo MiyamotoDepartment of Cellular and Molecular Physiology, Graduate School of Medicine, Yamaguchi University, Ube, Yamaguchi, Japan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Primary cilia are the microtubule-based sensory organelles. The unique lipid makeup of the ciliary membrane strictly controls their signaling ability, to orchestrate tissue formation and homeostasis. Emerging evidence has demonstrated that lipids play important roles in cilia formation and cilia-related signaling, solidifying the previously proposed concept of "lipid ciliology." The ciliary membrane exhibits a highly specialized lipid composition, including enrichment in cholesterol, sphingolipids, and specific phosphoinositides, compared with the surrounding plasma membrane. Recent studies have revealed that cholesterol and phosphoinositides function together to regulate ciliary homeostasis, protein trafficking, and signal transduction. A growing spectrum of ciliopathies, including polycystic kidney disease, retinal degeneration, cerebellar hypoplasia, and metabolic disorders, can be caused by dysregulation of lipid metabolism and lipid-modifying enzymes through impaired cilia-related signaling. Moreover, defects in cholesterol biosynthesis or intracellular lipid transport contribute to various ciliopathies, such as Smith-Lemli-Opitz syndrome and Zellweger spectrum disorders. In this review, we summarize recent advances in lipid ciliology, focusing on the underlying molecular mechanisms of ciliary cholesterol-dependent signaling in ciliopathies for emerging therapeutic strategies.

Indexed as

cholesterolciliopathieslipid ciliologyphosphoinositidesprimary cilia

Identifiers

PMID42553286
PMCPMC13433868

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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.