Targeting a novel apoptotic pathway in human disease.

IGFBP3 TMEM219 apoptosis intestinal stem cells pancreatic beta cells

Journal

BioEssays : news and reviews in molecular, cellular and developmental biology
ISSN: 1521-1878
Titre abrégé: Bioessays
Pays: United States
ID NLM: 8510851

Informations de publication

Date de publication:
06 2023
Historique:
revised: 09 03 2023
received: 30 11 2022
accepted: 15 03 2023
medline: 17 5 2023
pubmed: 31 3 2023
entrez: 30 3 2023
Statut: ppublish

Résumé

Apoptotic pathways have always been regarded as a key-player in preserving tissue and organ homeostasis. Excessive activation or resistance to activation of cell death signaling may indeed be responsible for several mechanisms of disease, including malignancy and chronic degenerative diseases. Therefore, targeting apoptotic factors gained more and more attention in the scientific community and novel strategies emerged aimed at selectively blocking or stimulating cell death signaling. This is also the case for the TMEM219 death receptor, which is activated by a circulating ligand, the Insulin-like growth factor binding protein 3 (IGFBP3) and induces a caspase-8-dependent apoptosis of the target cells. Interestingly, stimulation of the IGFBP3/TMEM219 axis exerts an anti-proliferative effect, while blockade of the TMEM219 deleterious signal protects TMEM219-expressing cells of the endocrine pancreas, lung, and intestine from damage and death. Here, we summarize the most updated reports on the role of the IGFBP3/TMEM219 apoptotic axis in disease conditions, including intestinal disorders and diabetes, and we describe the advancements in designing and testing novel TMEM219-based targeting approaches in emerging potential clinical applications.

Identifiants

pubmed: 36998110
doi: 10.1002/bies.202200231
doi:

Types de publication

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

Langues

eng

Sous-ensembles de citation

IM

Pagination

e2200231

Informations de copyright

© 2023 The Authors. BioEssays published by Wiley Periodicals LLC.

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Auteurs

Francesca D'Addio (F)

International Center for T1D, Pediatric Clinical Research Center Romeo ed Enrica Invernizzi, DIBIC, Università di Milano, Milan, Italy.
Division of Endocrinology, ASST Fatebenefratelli-Sacco, Milan, Italy.

Laura Montefusco (L)

Division of Endocrinology, ASST Fatebenefratelli-Sacco, Milan, Italy.

Maria Elena Lunati (ME)

Division of Endocrinology, ASST Fatebenefratelli-Sacco, Milan, Italy.

Ida Pastore (I)

Division of Endocrinology, ASST Fatebenefratelli-Sacco, Milan, Italy.

Emma Assi (E)

International Center for T1D, Pediatric Clinical Research Center Romeo ed Enrica Invernizzi, DIBIC, Università di Milano, Milan, Italy.

Adriana Petrazzuolo (A)

International Center for T1D, Pediatric Clinical Research Center Romeo ed Enrica Invernizzi, DIBIC, Università di Milano, Milan, Italy.

Virna Marin (V)

Enthera s.r.l.

Chiara Bruckmann (C)

Enthera s.r.l.

Paolo Fiorina (P)

International Center for T1D, Pediatric Clinical Research Center Romeo ed Enrica Invernizzi, DIBIC, Università di Milano, Milan, Italy.
Division of Endocrinology, ASST Fatebenefratelli-Sacco, Milan, Italy.
Nephrology Division, Boston Children's Hospital and Transplantation Research Center, Brigham and Women's Hospital, Harvard Medical School, Boston, Massachusetts, USA.

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