Cited by 322Pancreatic function and diabetesDiabetes and associated disordersDiabetes Treatment and Management

Long-Term GABA Administration Induces Alpha Cell-Mediated Beta-like Cell Neogenesis

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Ben-Othman, Nouha, Vieira, Andhira, Courtney, Monica, Record, Fabien, Gjernes, Elisabet, Avolio, Fabio, Hadzic, Biljana, Druelle, Noémie +16 more·2017·Cell

Abstract

The recent discovery that genetically modified α cells can regenerate and convert into β-like cells in vivo holds great promise for diabetes research. However, to eventually translate these findings to human, it is crucial to discover compounds with similar activities. Herein, we report the identification of GABA as an inducer of α-to-β-like cell conversion in vivo. This conversion induces α cell replacement mechanisms through the mobilization of duct-lining precursor cells that adopt an α cell identity prior to being converted into β-like cells, solely upon sustained GABA exposure. Importantly, these neo-generated β-like cells are functional and can repeatedly reverse chemically induced diabetes in vivo. Similarly, the treatment of transplanted human islets with GABA results in a loss of α cells and a concomitant increase in β-like cell counts, suggestive of α-to-β-like cell conversion processes also in humans. This newly discovered GABA-induced α cell-mediated β-like cell neogenesis could therefore represent an unprecedented hope toward improved therapies for diabetes.

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Crossref · 10.1016/j.cell.2016.11.002

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  • GABA induces conversion of mouse α-cells to β-cells in vivo.

    “Fascinatingly, GABA induces conversion of mouse α-cells to β-cells in vivo, and treatment of transplanted human islets with GABA results (via activation of GABAA receptors in α-cells) in an increased percentage of β-cells and a reduced percentage of α-cells, suggesting a similar conversion may occur in humans (55).”
  • Treatment of transplanted human islets with GABA results in an increased percentage of β-cells and a reduced percentage of α-cells.

    “Fascinatingly, GABA induces conversion of mouse α-cells to β-cells in vivo, and treatment of transplanted human islets with GABA results (via activation of GABAA receptors in α-cells) in an increased percentage of β-cells and a reduced percentage of α-cells, suggesting a similar conversion may occur in humans (55).”

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Research works printed but not linked: 2

  1. Collombat, P., Hecksher-Sorensen, J., Krull, J., Berger, J., Riedel, D., Herrera, P.L., Serup, P., and Mansouri, A. (2007). Embryonic endocrine pancreas and mature beta cells acquire alpha and PP cell phenotypes upon Arx misexpression. The Journal of clinical investigation 117, 961-970.
  2. Franklin, I.K., and Wollheim, C.B. (2004). GABA in the endocrine pancreas: its putative role as an islet cell paracrine-signalling molecule. The Journal of general physiology 123, 185-190.

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Authors
Ben-Othman, N., Vieira, A., Courtney, M., Record, F., Gjernes, E., Avolio, F., Hadzic, B., Druelle, N., Napolitano, T., Navarro-Sanz, S., Silvano, S., Al-Hasani, K., Pfeifer, A., Lacas-Gervais, S., Leuckx, G., Marroquí, L., Thévenet, J., Madsen, O. D., Eizirik, D. L., Heimberg, H., Kerr-Conte, J., Pattou, F., Mansouri, A., & Collombat, P.
Affiliations
  • Centre National de la Recherche Scientifique (FR)
  • Vrije Universiteit Brussel (BE)
  • Université Libre de Bruxelles (BE)
  • Inserm (FR)
  • University of Copenhagen (DK)
  • Max Planck Institute for Biophysical Chemistry (DE)
Corresponding author
Collombat, Patrick
Venue
Cell
Publisher
Elsevier BV
Published
2017-01
Volume
168
Issue
1-2
Pages
73-85.e11
ISSN
0092-8674 (ISSN-L)
OpenAlex
W2559389868
Cited by
322
References
2
Citations by year
2026: 12 · 2025: 26 · 2024: 26 · 2023: 30 · 2022: 33 · 2021: 35 · 2020: 41 · 2019: 39 · 2018: 38 · 2017: 41 · 2016: 1
FWCI
43.94
Type
journal article
Language
en
Open access
Locations
  • Cell (publishedVersion)
  • PubMed (publishedVersion)
  • HAL (submittedVersion)
  • Dépôt institutionnel de l'Université libre de Bruxelles (Université Libre de Bruxelles) (submittedVersion)
  • Research at the University of Copenhagen (University of Copenhagen) (submittedVersion)
  • MPG.PuRe (Max Planck Society) (submittedVersion)
  • VUBIR (Vrije Universiteit Brussel) (submittedVersion)
Funders
  • Juvenile Diabetes Research Foundation International (17-2011-16, 3-SRA-2014-282-Q-R, 2-2010-567, 17-2013-426)
  • Bundesministerium für Bildung und Forschung (2009 GENO 105 01/01KU0906)
  • Fondation pour la Recherche Médicale (DRC20091217179)
  • Institut National de la Santé et de la Recherche Médicale
  • Max-Planck-Gesellschaft
  • Agence Nationale de la Recherche
  • Fondation Générale de Santé
  • Stichting Diabetes Onderzoek Nederland
  • Fonds De La Recherche Scientifique - FNRS (G034613N, G024512N)
  • European Research Council (StG-2011-281265)
  • Fonds Wetenschappelijk Onderzoek
  • Fondation Schlumberger pour l’Education et la Recherche
  • Leona M. and Harry B. Helmsley Charitable Trust (ANR-10-LABX-46, 31-2008-416, CR-2015A-06)
Topics
  • Health Sciences › Medicine › Surgery › Pancreatic function and diabetes
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Diabetes and associated disorders
  • Health Sciences › Medicine › Endocrinology, Diabetes and Metabolism › Diabetes Treatment and Management
Keywords
GABA, islet regeneration, chemically induced diabetes, diabetes treatment, human islet transplantation, pancreatic islets
MeSH terms
Animals, Cell Differentiation, Diabetes Mellitus, gamma-Aminobutyric Acid, Humans, Islets of Langerhans, Male, Nerve Tissue Proteins, Rats, Wistar, Glucagon-Secreting Cells, Insulin-Secreting Cells, Mice, Rats, Basic Helix-Loop-Helix Transcription Factors, Basic Helix-Loop-Helix Proteins

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