Wound healing in aged skin exhibits systems-level alterations in cellular composition and cell-cell communication.

CP: Cell biology CP: Developmental biology aging cell-cell communication cellular heterogeneity dendritic cell macrophage neutrophil signaling single-cell RNA-seq skin wound healing

Journal

Cell reports
ISSN: 2211-1247
Titre abrégé: Cell Rep
Pays: United States
ID NLM: 101573691

Informations de publication

Date de publication:
02 08 2022
Historique:
received: 09 12 2021
revised: 13 05 2022
accepted: 12 07 2022
entrez: 4 8 2022
pubmed: 5 8 2022
medline: 9 8 2022
Statut: ppublish

Résumé

Delayed and often impaired wound healing in the elderly presents major medical and socioeconomic challenges. A comprehensive understanding of the cellular/molecular changes that shape complex cell-cell communications in aged skin wounds is lacking. Here, we use single-cell RNA sequencing to define the epithelial, fibroblast, immune cell types, and encompassing heterogeneities in young and aged skin during homeostasis and identify major changes in cell compositions, kinetics, and molecular profiles during wound healing. Our comparative study uncovers a more pronounced inflammatory phenotype in aged skin wounds, featuring neutrophil persistence and higher abundance of an inflammatory/glycolytic Arg1

Identifiants

pubmed: 35926463
pii: S2211-1247(22)00964-0
doi: 10.1016/j.celrep.2022.111155
pmc: PMC9901190
mid: NIHMS1866797
pii:
doi:

Types de publication

Journal Article Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, Non-P.H.S.

Langues

eng

Sous-ensembles de citation

IM

Pagination

111155

Subventions

Organisme : NIAMS NIH HHS
ID : R01 AR068074
Pays : United States
Organisme : NIGMS NIH HHS
ID : R01 GM123731
Pays : United States
Organisme : NIGMS NIH HHS
ID : R35 GM145307
Pays : United States
Organisme : NIAMS NIH HHS
ID : U01 AR073159
Pays : United States
Organisme : NIAMS NIH HHS
ID : P30 AR075047
Pays : United States

Informations de copyright

Copyright © 2022 The Author(s). Published by Elsevier Inc. All rights reserved.

Déclaration de conflit d'intérêts

Declaration of interests The authors declare no competing interests.

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Auteurs

Remy Vu (R)

Department of Biological Chemistry, School of Medicine, University of California, Irvine, Irvine, CA 92697, USA; The NSF-Simons Center for Multiscale Cell Fate Research, University of California, Irvine, Irvine, CA 92627, USA.

Suoqin Jin (S)

School of Mathematics and Statistics, Wuhan University, Wuhan 430072, China; Department of Mathematics, University of California, Irvine, Irvine, CA 92697, USA.

Peng Sun (P)

Department of Biological Chemistry, School of Medicine, University of California, Irvine, Irvine, CA 92697, USA; The NSF-Simons Center for Multiscale Cell Fate Research, University of California, Irvine, Irvine, CA 92627, USA.

Daniel Haensel (D)

Department of Biological Chemistry, School of Medicine, University of California, Irvine, Irvine, CA 92697, USA; The NSF-Simons Center for Multiscale Cell Fate Research, University of California, Irvine, Irvine, CA 92627, USA.

Quy Hoa Nguyen (QH)

Department of Biological Chemistry, School of Medicine, University of California, Irvine, Irvine, CA 92697, USA.

Morgan Dragan (M)

Department of Biological Chemistry, School of Medicine, University of California, Irvine, Irvine, CA 92697, USA; The NSF-Simons Center for Multiscale Cell Fate Research, University of California, Irvine, Irvine, CA 92627, USA.

Kai Kessenbrock (K)

Department of Biological Chemistry, School of Medicine, University of California, Irvine, Irvine, CA 92697, USA.

Qing Nie (Q)

The NSF-Simons Center for Multiscale Cell Fate Research, University of California, Irvine, Irvine, CA 92627, USA; Department of Mathematics, University of California, Irvine, Irvine, CA 92697, USA; Department of Developmental and Cell Biology, University of California, Irvine, Irvine, CA 92697, USA. Electronic address: qnie@uci.edu.

Xing Dai (X)

Department of Biological Chemistry, School of Medicine, University of California, Irvine, Irvine, CA 92697, USA; The NSF-Simons Center for Multiscale Cell Fate Research, University of California, Irvine, Irvine, CA 92627, USA. Electronic address: xdai@uci.edu.

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