β Cell and Autophagy: What Do We Know?

Author:

Mohammadi-Motlagh Hamid-Reza1ORCID,Sadeghalvad Mona2,Yavari Niloofar3,Primavera Rosita4ORCID,Soltani Setareh5,Chetty Shashank4,Ganguly Abantika4ORCID,Regmi Shobha4,Fløyel Tina6ORCID,Kaur Simranjeet6ORCID,Mirza Aashiq H.67,Thakor Avnesh S.4ORCID,Pociot Flemming68ORCID,Yarani Reza46ORCID

Affiliation:

1. Medical Biology Research Center, Health Technology Institute, Kermanshah University of Medical Sciences, Kermanshah 67155-1616, Iran

2. Department of Immunology, School of Medicine, Tehran University of Medical Sciences, Tehran 1416634793, Iran

3. Department of Cellular and Molecular Medicine, The Panum Institute, Faculty of Health and Medical Sciences, University of Copenhagen, 2200 Copenhagen, Denmark

4. Interventional Regenerative Innovation at Stanford (IRIS), Department of Radiology, Stanford University School of Medicine, Palo Alto, CA 94304, USA

5. Clinical Research Development Center, Taleghani and Imam Ali Hospital, Kermanshah University of Medical Sciences, Kermanshah 67145-1673, Iran

6. Translational Type 1 Diabetes Research, Department of Clinical Research, Steno Diabetes Center Copenhagen, 2730 Herlev, Denmark

7. Department of Pharmacology, Weill Cornell Medicine, New York, NY 10065, USA

8. Institute for Clinical Medicine, Faculty of Health and Medical Sciences, University of Copenhagen, 2200 Copenhagen, Denmark

Abstract

Pancreatic β cells are central to glycemic regulation through insulin production. Studies show autophagy as an essential process in β cell function and fate. Autophagy is a catabolic cellular process that regulates cell homeostasis by recycling surplus or damaged cell components. Impaired autophagy results in β cell loss of function and apoptosis and, as a result, diabetes initiation and progress. It has been shown that in response to endoplasmic reticulum stress, inflammation, and high metabolic demands, autophagy affects β cell function, insulin synthesis, and secretion. This review highlights recent evidence regarding how autophagy can affect β cells’ fate in the pathogenesis of diabetes. Furthermore, we discuss the role of important intrinsic and extrinsic autophagy modulators, which can lead to β cell failure.

Funder

The Lundbeck foundation

Stanford Maternal and Child Health Research Institute

Publisher

MDPI AG

Subject

Molecular Biology,Biochemistry

Cited by 3 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献

1. Pharmacological targets at the lysosomal autophagy–NLRP3 inflammasome crossroads;Trends in Pharmacological Sciences;2024-01

2. Pancreatic islet cell plasticity: Pathogenic or therapeutically exploitable?;Diabetes, Obesity and Metabolism;2023-10-16

3. Mitochondrial Dynamics and Insulin Secretion;International Journal of Molecular Sciences;2023-09-07

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