Intrinsic heterogeneity of primary cilia revealed through spatial proteomics

Primary cilia are critical organelles found on most human cells. Their dysfunction is linked to hereditary ciliopathies with a wide phenotypic spectrum. Despite their significance, the specific roles of cilia in different cell types remain poorly understood due to limitations in analyzing ciliary protein composition. We employed antibody-based spatial proteomics to expand the Human Protein Atlas to primary cilia. Our analysis identified the subciliary locations of 715 proteins across three cell lines, examining 128,156 individual cilia. We found that 69% of the ciliary proteome is cell-type specific, and 78% exhibited single-cilia heterogeneity. Our findings portray cilia as sensors tuning their proteome to effectively sense the environment and compute cellular responses. We reveal 91 cilia proteins and found a genetic candidate variant in CREB3 in one clinical case with features overlapping ciliopathy phenotypes. This open, spatial cilia atlas advances research on cilia and ciliopathies.

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Publication Details

Journal
Cell
Published
2025-09-26
DOI
https://doi.org/10.1016/j.cell.2025.08.039
Citations
17
Primary Topic
Genetic and Kidney Cyst Diseases
Type
article
Field-Weighted Citation Impact
30.89
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article

Intrinsic heterogeneity of primary cilia revealed through spatial proteomics

Angelica Maria Delgado-Vega, Anna Bäckström, Diana Mahdessian, Cecilia Lindskog et al.
17 citations
Cell
Genetic and Kidney Cyst Diseases
30.89
article

Intrinsic heterogeneity of primary cilia revealed through spatial proteomics

Angelica Maria Delgado-Vega, Anna Bäckström, Diana Mahdessian, Cecilia Lindskog, Shu‐Hsien Sheu, Fredric Johansson, Kalle von Feilitzen, Anna Martinez Casals, César Villegas, Emma K. Lundberg, Huangqingbo Sun, Konstantin Kahnert, Mathias Uhlén, Jan N. Hansen, Jenny Fall, Ulrika Axelsson, Eini Westenius, Trang Le, Casper F. Winsnes, Anna Lindstrand, Anders Johannesson, Emmie Pohjanen, Frederic Ballllosera Navarro, Kalliopi Tzavlaki, Anna Mäkiniemi
article en
17 citations

Abstract

Primary cilia are critical organelles found on most human cells. Their dysfunction is linked to hereditary ciliopathies with a wide phenotypic spectrum. Despite their significance, the specific roles of cilia in different cell types remain poorly understood due to limitations in analyzing ciliary protein composition. We employed antibody-based spatial proteomics to expand the Human Protein Atlas to primary cilia. Our analysis identified the subciliary locations of 715 proteins across three cell lines, examining 128,156 individual cilia. We found that 69% of the ciliary proteome is cell-type specific, and 78% exhibited single-cilia heterogeneity. Our findings portray cilia as sensors tuning their proteome to effectively sense the environment and compute cellular responses. We reveal 91 cilia proteins and found a genetic candidate variant in CREB3 in one clinical case with features overlapping ciliopathy phenotypes. This open, spatial cilia atlas advances research on cilia and ciliopathies.

CellVol. 188(24)
Uppsala University (SE), Science for Life Laboratory (SE), Chan Zuckerberg Initiative (United States) (US), Ludwig Cancer Research (SE), KTH Royal Institute of Technology (SE), Stanford University (US)
Openalex Percentile: Top 0%
Genetic and Kidney Cyst Diseases
30.89
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