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Diabetologia. 2018 Oct;61(10):2202-2214. doi: 10.1007/s00125-018-4687-y. Epub 2018 Jul 21.

MANF protects human pancreatic beta cells against stress-induced cell death.

Author information

1
Research Programs Unit, Molecular Neurology, Biomedicum Helsinki, University of Helsinki, PO Box 63, (Haartmaninkatu 8), 00014, Helsinki, Finland.
2
Children's Hospital, University of Helsinki and Helsinki University Central Hospital, Helsinki, Finland.
3
Research Programs Unit, Molecular Neurology, Biomedicum Helsinki, University of Helsinki, PO Box 63, (Haartmaninkatu 8), 00014, Helsinki, Finland. vikash.chandra@helsinki.fi.
4
Clinicum, Faculty of Medicine, University of Helsinki, Helsinki, Finland.
5
Department of Biosciences and Nutrition, Karolinska Institutet, Huddinge, Sweden.
6
Research Program in Developmental Biology, Institute of Biotechnology, University of Helsinki, Helsinki, Finland.
7
The Folkhälsan Institute of Genetics, Helsinki, Finland.
8
Competence Centre on Health Technologies, Tartu, Estonia.
9
Department of Medical and Molecular Genetics, King's College London, London, UK.
10
Research Programs Unit, Molecular Neurology, Biomedicum Helsinki, University of Helsinki, PO Box 63, (Haartmaninkatu 8), 00014, Helsinki, Finland. timo.otonkoski@helsinki.fi.
11
Children's Hospital, University of Helsinki and Helsinki University Central Hospital, Helsinki, Finland. timo.otonkoski@helsinki.fi.

Abstract

AIMS/HYPOTHESIS:

There is a great need to identify factors that could protect pancreatic beta cells against apoptosis or stimulate their replication and thus prevent or reverse the development of diabetes. One potential candidate is mesencephalic astrocyte-derived neurotrophic factor (MANF), an endoplasmic reticulum (ER) stress inducible protein. Manf knockout mice used as a model of diabetes develop the condition because of increased apoptosis and reduced proliferation of beta cells, apparently related to ER stress. Given this novel association between MANF and beta cell death, we studied the potential of MANF to protect human beta cells against experimentally induced ER stress.

METHODS:

Primary human islets were challenged with proinflammatory cytokines, with or without MANF. Cell viability was analysed and global transcriptomic analysis performed. Results were further validated using the human beta cell line EndoC-βH1.

RESULTS:

There was increased expression and secretion of MANF in human beta cells in response to cytokines. Addition of recombinant human MANF reduced cytokine-induced cell death by 38% in human islets (p < 0.05). MANF knockdown in EndoC-βH1 cells led to increased ER stress after cytokine challenge. Mechanistic studies showed that the protective effect of MANF was associated with repression of the NF-κB signalling pathway and amelioration of ER stress. MANF also increased the proliferation of primary human beta cells twofold when TGF-β signalling was inhibited (p < 0.01).

CONCLUSIONS/INTERPRETATION:

Our studies show that exogenous MANF protein can provide protection to human beta cells against death induced by inflammatory stress. The antiapoptotic and mitogenic properties of MANF make it a potential therapeutic agent for beta cell protection.

KEYWORDS:

Beta cell proliferation; Beta cell protection; Endoplasmic reticulum stress; Mesencephalic astrocyte-derived neurotrophic factor (MANF); NF-κB

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