Chloroquine alleviates the heat-induced to injure via autophagy and apoptosis mechanisms in skin cell and mouse models

Burns can cause cell death and irreversible tissue damage. We examined the pathway of human dermis fibroblasts cell death caused by skin burns and the roles of chloroquine in human skin keratinocytes HaCaT wound healing. Western blot assays were performed to assess expression of proteins associated with autophagy, apoptosis, and endoplasmic reticulum stress in skin cells following burns. Changes in apoptosis-related proteins were assessed using flow cytometry, and wound cell migration was examined using wound healing assays. The burn animal model was used to test whether chloroquine would promote wound healing. In human burned fibroblasts, expression of LC3B-II and Cleave-caspase-7 was increased, whereas expression of Beclin-1, p62, and Grp78 was decreased. Severe burn induced ER stress and ERK phosphorylation, but PD98059 or necrostatin-1 treatment cells did not affect expression of autophagy LC3B-II protein and can induce apoptosis. Even though added with TGF-β and FGF did not repair autophagy caused by burns. Suggesting that autophagy and apoptosis were involved in heat-injured mechanism. Recombinant Wnt3a protein can help restore expression of β-catenin which reduced following burns in keratinocytes. Wnt3a protein can promote migration of keratinocytes after burns. Interesting, chloroquine increased expression of LC3B-II protein and restored cell migration activity after 24 h of burns. Consistently, surgical dressing containing chloroquine promoted wound healing in a burn animal mode. Autophagy and Wnt/β-catenin is two signalling pathways that participate in cell repair and wound healing in human fibroblasts, keratinocytes. Surgical dressing containing chloroquine can recover wound healing in burned rats.

Medienart:

E-Artikel

Erscheinungsjahr:

2022

Erschienen:

2022

Enthalten in:

Zur Gesamtaufnahme - volume:17

Enthalten in:

PloS one - 17(2022), 8 vom: 09., Seite e0272797

Sprache:

Englisch

Beteiligte Personen:

Tang, Sheau-Chung [VerfasserIn]
Ko, Jiunn-Liang [VerfasserIn]
Lu, Chun-Te [VerfasserIn]
Leong, Pui-Ying [VerfasserIn]
Ou, Chu-Chyn [VerfasserIn]
Hsu, Chih-Ting [VerfasserIn]
Hsiao, Yu-Ping [VerfasserIn]

Links:

Volltext

Themen:

886U3H6UFF
Apoptosis Regulatory Proteins
Beta Catenin
Chloroquine
Journal Article
Wnt3A Protein

Anmerkungen:

Date Completed 08.09.2022

Date Revised 14.09.2022

published: Electronic-eCollection

Citation Status MEDLINE

doi:

10.1371/journal.pone.0272797

funding:

Förderinstitution / Projekttitel:

PPN (Katalog-ID):

NLM345617681