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Toll-like receptors TLR2 and TLR4 block the replication of pancreatic β cells in diet-induced obesity

Consumption of high energy Western diet triggers mild adaptive β cell proliferation to compensate for peripheral insulin resistance; however, the underlying molecular mechanism remains unclear. Here we show that the Toll-like receptors TLR2 and TLR4 inhibited the diet-induced replication of β cells...

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Detalles Bibliográficos
Autores principales: Ji, Yewei, Sun, Shengyi, Shrestha, Neha, Darragh, Laurel B., Shirakawa, Jun, Xing, Yuan, He, Yi, Carboneau, Bethany A., Kim, Hana, An, Duo, Ma, Minglin, Oberhozler, Jose, Soleimanpour, Scott A., Gannon, Maureen, Liu, Chengyang, Naji, Ali, Kulkarni, Rohit N., Wang, Yong, Kersten, Sander, Qi, Ling
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6531334/
https://www.ncbi.nlm.nih.gov/pubmed/31110312
http://dx.doi.org/10.1038/s41590-019-0396-z
Descripción
Sumario:Consumption of high energy Western diet triggers mild adaptive β cell proliferation to compensate for peripheral insulin resistance; however, the underlying molecular mechanism remains unclear. Here we show that the Toll-like receptors TLR2 and TLR4 inhibited the diet-induced replication of β cells in mice and humans. The combined, but not the individual loss of TLR2 and TLR4 increased the replication of β cells, but not that of α cells, leading to enlarged β cell area and hyperinsulinemia in diet-induced obesity. Loss of TLR2 and TLR4 increased the nuclear abundance of the cell cycle regulators cyclin D2 and Cdk4 in a manner dependent on the signaling mediator Erk. These data reveal a regulatory mechanism controlling the proliferation of β cells in diet-induced obesity and suggest that selective targeting of the TLR2-TLR4 pathways may reverse β cell failure in diabetic patients.