HaCaT cells as a model system to study primary cilia in keratinocytes.


Journal

Experimental dermatology
ISSN: 1600-0625
Titre abrégé: Exp Dermatol
Pays: Denmark
ID NLM: 9301549

Informations de publication

Date de publication:
08 2022
Historique:
revised: 09 05 2022
received: 03 01 2022
accepted: 13 06 2022
pubmed: 17 6 2022
medline: 19 8 2022
entrez: 16 6 2022
Statut: ppublish

Résumé

Primary cilium (PC) is a microtubule-based organelle found on the apical surface of most mammalian cell types, playing a role in development and tissue homeostasis. Ciliopathies are a rapidly growing group of human diseases characterized by disordered cilium. PC plays an important role in pathogenesis of basal cell cancer, the most common human malignancy. A significant increase in ciliation has been observed in the epidermis of atopic dermatitis and psoriasis patients. Spontaneously immortalized human keratinocytes, HaCaT are a model to study the epidermal homeostasis and pathophysiology. In contrast to what has been previously described, here, we show that HaCaT can be efficiently ciliated. In HaCaT cells, differentiation significantly increased the number of ciliated cells and we were able to analyse in detail the ciliary length progression with duration of differentiation. As the number of recognized ciliopathies continues to increase, the importance of ciliary models also rises. Even though keratinocytes do not become as highly and rapidly ciliated as cell lines frequently used in ciliary studies, they are a better model for the study of skin ciliopathies. Detailed progression of ciliation in HaCaT could serve as the basis for ciliary studies in this cell line.

Identifiants

pubmed: 35708968
doi: 10.1111/exd.14626
pmc: PMC9542831
doi:

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

1276-1280

Informations de copyright

© 2022 The Authors. Experimental Dermatology published by John Wiley & Sons Ltd.

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Auteurs

Gabriela Blanchard (G)

Department of Dermatology, CHUV-FBM UNIL, Beaumont Hospital, Lausanne, Switzerland.

Christine Pich (C)

Department of Dermatology, CHUV-FBM UNIL, Beaumont Hospital, Lausanne, Switzerland.

Daniel Hohl (D)

Department of Dermatology, CHUV-FBM UNIL, Beaumont Hospital, Lausanne, Switzerland.
University of Lausanne, Lausanne, Switzerland.

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