Preadipocyte factor 1 induces pancreatic ductal cell differentiation into insulin-producing cells

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作者
Marie Rhee
Seung-Hwan Lee
Ji-Won Kim
Dong-Sik Ham
Heon-Seok Park
Hae Kyung Yang
Ju-Young Shin
Jae-Hyoung Cho
Young-Bum Kim
Byung-Soo Youn
Hei Sook Sul
Kun-Ho Yoon
机构
[1] College of Medicine,Division of Endocrinology and Metabolism, Department of Internal Medicine
[2] The Catholic University of Korea,Division of Endocrinology
[3] Convergent Research Consortium for Immunologic Disease,Department of Nutritional Science and Toxicology
[4] Catholic Research Institutes of Medical Science,undefined
[5] The Catholic University of Korea,undefined
[6] Diabetes and Metabolism,undefined
[7] Beth Israel Deaconess Medical Center and Harvard Medical School,undefined
[8] Biomedical Research Center,undefined
[9] Ulsan University Hospital,undefined
[10] University of Ulsan College of Medicine,undefined
[11] University of California,undefined
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摘要
The preadipocyte factor 1 (Pref-1) is involved in the proliferation and differentiation of various precursor cells. However, the intracellular signaling pathways that control these processes and the role of Pref-1 in the pancreas remain poorly understood. Here, we showed that Pref-1 induces insulin synthesis and secretion via two independent pathways. The overexpression of Pref-1 activated MAPK signaling, which induced nucleocytoplasmic translocation of FOXO1 and PDX1 and led to the differentiation of human pancreatic ductal cells into β-like cells and an increase in insulin synthesis. Concurrently, Pref-1 activated Akt signaling and facilitated insulin secretion. A proteomics analysis identified the Rab43 GTPase-activating protein as a downstream target of Akt. A serial activation of both proteins induced various granular protein syntheses which led to enhanced glucose-stimulated insulin secretion. In a pancreatectomised diabetic animal model, exogenous Pref-1 improved glucose homeostasis by accelerating pancreatic ductal and β-cell regeneration after injury. These data establish a novel role for Pref-1, opening the possibility of applying this molecule to the treatment of diabetes.
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