Proteomic Identification Reveals the Role of Ciliary Extracellular-Like Vesicle in Cardiovascular Function.

aortic stenosis arrythmia cardiac edema extracellular vesicles fibrosis hypotension primary cilia

Journal

Advanced science (Weinheim, Baden-Wurttemberg, Germany)
ISSN: 2198-3844
Titre abrégé: Adv Sci (Weinh)
Pays: Germany
ID NLM: 101664569

Informations de publication

Date de publication:
Aug 2020
Historique:
received: 04 11 2019
revised: 07 04 2020
entrez: 25 8 2020
pubmed: 25 8 2020
medline: 25 8 2020
Statut: epublish

Résumé

Primary cilia are shown to have membrane swelling, also known as ciliary bulbs. However, the role of these structures and their physiological relevance remains unknown. Here, it is reported that a ciliary bulb has extracellular vesicle (EV)-like characteristics. The ciliary extracellular-like vesicle (cELV) has a unique dynamic movement and can be released by mechanical fluid force. To better identify the cELV, differential multidimensional proteomic analyses are performed on the cELV. A database of 172 cELV proteins is generated, and all that examined are confirmed to be in the cELV. Repressing the expression of these proteins in vitro and in vivo inhibits cELV formation. In addition to the randomized heart looping, hydrocephalus, and cystic kidney in fish, compensated heart contractility is observed in both fish and mouse models. Specifically, low circulation of cELV results in hypotension with compensated heart function, left ventricular hypertrophy, cardiac fibrosis, and arrhythmogenic characteristics, which result in a high mortality rate in mice. Furthermore, the overall ejection fraction, stroke volume, and cardiac output are significantly decreased in mice lacking cELV. It is thus proposed that the cELV as a nanocompartment within a primary cilium plays an important role in cardiovascular functions.

Identifiants

pubmed: 32832346
doi: 10.1002/advs.201903140
pii: ADVS1763
pmc: PMC7435257
doi:

Types de publication

Journal Article

Langues

eng

Pagination

1903140

Informations de copyright

© 2020 The Authors. Published by WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim.

Déclaration de conflit d'intérêts

The authors declare no conflict of interest.

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Auteurs

Ashraf M Mohieldin (AM)

Department of Biomedical and Pharmaceutical Sciences Chapman University Irvine CA 92618 USA.

Rajasekharreddy Pala (R)

Department of Biomedical and Pharmaceutical Sciences Chapman University Irvine CA 92618 USA.

Rinzhin T Sherpa (RT)

Department of Biomedical and Pharmaceutical Sciences Chapman University Irvine CA 92618 USA.

Madhawi Alanazi (M)

Department of Biomedical and Pharmaceutical Sciences Chapman University Irvine CA 92618 USA.

Ashwaq Alanazi (A)

Department of Biomedical and Pharmaceutical Sciences Chapman University Irvine CA 92618 USA.

Kiumars Shamloo (K)

Department of Biomedical and Pharmaceutical Sciences Chapman University Irvine CA 92618 USA.

Amir Ahsan (A)

Department of Physics, Computer Science and Engineering Chapman University Orange CA 92866 USA.

Wissam A AbouAlaiwi (WA)

Department of Pharmacology and Experimental Therapeutics University of Toledo Toledo OH 43614 USA.

James J Moresco (JJ)

Department of Molecular Medicine The Scripps Research Institute La Jolla CA 92037 USA.

John R Yates (JR)

Department of Molecular Medicine The Scripps Research Institute La Jolla CA 92037 USA.

Surya M Nauli (SM)

Department of Biomedical and Pharmaceutical Sciences Chapman University Irvine CA 92618 USA.
Department of Medicine University of California Irvine Irvine CA 92868 USA.

Classifications MeSH