Galectin 1-A Key Player between Tissue Repair and Fibrosis.

diabetic nephropathy diabetic retinopathy fibrosis galectin 1 idiopathic pulmonary fibrosis liver fibrosis pancreatic fibrosis wound healing

Journal

International journal of molecular sciences
ISSN: 1422-0067
Titre abrégé: Int J Mol Sci
Pays: Switzerland
ID NLM: 101092791

Informations de publication

Date de publication:
16 May 2022
Historique:
received: 31 03 2022
revised: 13 05 2022
accepted: 13 05 2022
entrez: 28 5 2022
pubmed: 29 5 2022
medline: 1 6 2022
Statut: epublish

Résumé

Galectins are ten family members of carbohydrate-binding proteins with a high affinity for β galactose-containing oligosaccharides. Galectin-1 (Gal-1) is the first protein discovered in the family, expressed in many sites under normal and pathological conditions. In the first part of the review article, we described recent advances in the Gal-1 modulatory role on wound healing, by focusing on the different phases triggered by Gal-1, such as inflammation, proliferation, tissue repair and re-epithelialization. On the contrary, Gal-1 persistent over-expression enhances angiogenesis and extracellular matrix (ECM) production via PI3K/Akt pathway activation and leads to keloid tissue. Therefore, the targeted Gal-1 modulation should be considered a method of choice to treat wound healing and avoid keloid formation. In the second part of the review article, we discuss studies clarifying the role of Gal-1 in the pathogenesis of proliferative diabetic retinopathy, liver, renal, pancreatic and pulmonary fibrosis. This evidence suggests that Gal-1 may become a biomarker for the diagnosis and prognosis of tissue fibrosis and a promising molecular target for the development of new and original therapeutic tools to treat fibrosis in different chronic diseases.

Identifiants

pubmed: 35628357
pii: ijms23105548
doi: 10.3390/ijms23105548
pmc: PMC9142121
pii:
doi:

Substances chimiques

Galectin 1 0

Types de publication

Journal Article Review

Langues

eng

Sous-ensembles de citation

IM

Subventions

Organisme : Romanian Ministry of Research, Innovation and Digitization, CNCS/CCCDI - UEFISCDI
ID : PN-III-P4-ID-PCE-2020-1772

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Auteurs

Anca Hermenean (A)

Faculty of Medicine, Vasile Goldis Western University of Arad, 310414 Arad, Romania.
"Aurel Ardelean" Institute of Life Sciences, Vasile Goldis Western University of Arad, 310414 Arad, Romania.

Daniela Oatis (D)

Faculty of Medicine, Vasile Goldis Western University of Arad, 310414 Arad, Romania.

Hildegard Herman (H)

"Aurel Ardelean" Institute of Life Sciences, Vasile Goldis Western University of Arad, 310414 Arad, Romania.

Alina Ciceu (A)

"Aurel Ardelean" Institute of Life Sciences, Vasile Goldis Western University of Arad, 310414 Arad, Romania.

Giovanbattista D'Amico (G)

"Aurel Ardelean" Institute of Life Sciences, Vasile Goldis Western University of Arad, 310414 Arad, Romania.

Maria Consiglia Trotta (MC)

Department of Experimental Medicine, University of Campania "Luigi Vanvitelli", 80138 Naples, Italy.

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Classifications MeSH