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Identification of a small molecule that stimulates human β-cell proliferation and insulin secretion, and protects against cytotoxic stress in rat insulinoma cells.

Publication ,  Journal Article
Hohmeier, HE; Zhang, L; Taylor, B; Stephens, S; Lu, D; McNamara, P; Laffitte, B; Newgard, CB
Published in: PLoS One
2020

A key event in the development of both major forms of diabetes is the loss of functional pancreatic islet β-cell mass. Strategies aimed at enhancing β-cell regeneration have long been pursued, but methods for reliably inducing human β-cell proliferation with full retention of key functions such as glucose-stimulated insulin secretion (GSIS) are still very limited. We have previously reported that overexpression of the homeobox transcription factor NKX6.1 stimulates β-cell proliferation, while also enhancing GSIS and providing protection against β-cell cytotoxicity through induction of the VGF prohormone. We developed an NKX6.1 pathway screen by stably transfecting 832/13 rat insulinoma cells with a VGF promoter-luciferase reporter construct, using the resultant cell line to screen a 630,000 compound chemical library. We isolated three compounds with consistent effects to stimulate human islet cell proliferation, but not expression of NKX6.1 or VGF, suggesting an alternative mechanism of action. Further studies of the most potent of these compounds, GNF-9228, revealed that it selectively activates human β-cell relative to α-cell proliferation and has no effect on δ-cell replication. In addition, pre-treatment, but not short term exposure of human islets to GNF-9228 enhances GSIS. GNF-9228 also protects 832/13 insulinoma cells against ER stress- and inflammatory cytokine-induced cytotoxicity. GNF-9228 stimulates proliferation via a mechanism distinct from recently emergent DYRK1A inhibitors, as it is unaffected by DYRK1A overexpression and does not activate NFAT translocation. In conclusion, we have identified a small molecule with pleiotropic positive effects on islet biology, including stimulation of human β-cell proliferation and insulin secretion, and protection against multiple agents of cytotoxic stress.

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Published In

PLoS One

DOI

EISSN

1932-6203

Publication Date

2020

Volume

15

Issue

3

Start / End Page

e0224344

Location

United States

Related Subject Headings

  • Rats
  • Protein-Tyrosine Kinases
  • Protein Serine-Threonine Kinases
  • Protein Kinase Inhibitors
  • Neoplasm Proteins
  • Insulinoma
  • Insulin-Secreting Cells
  • Insulin Secretion
  • Humans
  • Homeodomain Proteins
 

Citation

APA
Chicago
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Hohmeier, H. E., Zhang, L., Taylor, B., Stephens, S., Lu, D., McNamara, P., … Newgard, C. B. (2020). Identification of a small molecule that stimulates human β-cell proliferation and insulin secretion, and protects against cytotoxic stress in rat insulinoma cells. PLoS One, 15(3), e0224344. https://doi.org/10.1371/journal.pone.0224344
Hohmeier, Hans E., Lu Zhang, Brandon Taylor, Samuel Stephens, Danhong Lu, Peter McNamara, Bryan Laffitte, and Christopher B. Newgard. “Identification of a small molecule that stimulates human β-cell proliferation and insulin secretion, and protects against cytotoxic stress in rat insulinoma cells.PLoS One 15, no. 3 (2020): e0224344. https://doi.org/10.1371/journal.pone.0224344.
Hohmeier, Hans E., et al. “Identification of a small molecule that stimulates human β-cell proliferation and insulin secretion, and protects against cytotoxic stress in rat insulinoma cells.PLoS One, vol. 15, no. 3, 2020, p. e0224344. Pubmed, doi:10.1371/journal.pone.0224344.
Hohmeier HE, Zhang L, Taylor B, Stephens S, Lu D, McNamara P, Laffitte B, Newgard CB. Identification of a small molecule that stimulates human β-cell proliferation and insulin secretion, and protects against cytotoxic stress in rat insulinoma cells. PLoS One. 2020;15(3):e0224344.

Published In

PLoS One

DOI

EISSN

1932-6203

Publication Date

2020

Volume

15

Issue

3

Start / End Page

e0224344

Location

United States

Related Subject Headings

  • Rats
  • Protein-Tyrosine Kinases
  • Protein Serine-Threonine Kinases
  • Protein Kinase Inhibitors
  • Neoplasm Proteins
  • Insulinoma
  • Insulin-Secreting Cells
  • Insulin Secretion
  • Humans
  • Homeodomain Proteins