Insulinotropic hormone glucagon-like peptide-1 differentiation of human pancreatic islet-derived progenitor cells into insulin-producing cells

被引:246
作者
Abraham, EJ [1 ]
Leech, CA [1 ]
Lin, JC [1 ]
Zulewski, H [1 ]
Habener, JF [1 ]
机构
[1] Harvard Univ, Mol Endocrinol Lab, Massachusetts Gen Hosp, Sch Med,Howard Hughes Med Inst, Boston, MA 02114 USA
关键词
D O I
10.1210/en.143.8.3152
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Glucagon-like peptide-1 (GLP-1) is an intestinal incretin hormone, derived from the processing of proglucagon, that exerts insulinotropic actions on insulin-producing pancreatic islet beta-cells. Recently GLP-1 was shown to stimulate the growth and differentiation (neogenesis) of beta-cells and appears to do so by inducing the expression of the homeodomain protein IDX-1 (islet duodenum homeobox-1; also known as PDX-1, pancreatic and duodenal homeobox gene; and as IPF-1, insulin promoter factor), which is required for pancreas development and the expression of beta-cell-specifie genes. Earlier we identified multipotential progenitor cells in the islet and ducts of the pancreas, termed nestin-positive islet-derived progenitor cells (NIPs). Here we report the expression of functional GLP-1 receptors on NIPs and that GLP-1 stimulates the differentiation of NIPs into insulin-producing cells. Furthermore, confluent NIP cultures express the proglucagon gene and secrete GLP-1. These findings suggest a model of islet development in which pancreatic progenitor cells express both GLP-1 receptors and proglucagon with the formation of GLP-1. Locally produced GLP-1 may act as an autocrine/paracrine developmental morphogen on receptors on NIPs, resulting in the activation of IDX-1 and the expression of the proinsulin gene conferring a beta-cell phenotype. GLP-1 may be an important morphogen both for the embryonic development of the pancreas and for the neogenesis of beta-cells in the islets of the adult pancreas.
引用
收藏
页码:3152 / 3161
页数:10
相关论文
共 50 条
  • [41] Insulin promoter factor-1 gene mutation linked to early-onset type 2 diabetes mellitus directs expression of a dominant negative isoprotein
    Stoffers, DA
    Stanojevic, V
    Habener, JF
    [J]. JOURNAL OF CLINICAL INVESTIGATION, 1998, 102 (01) : 232 - 241
  • [42] Insulinotropic glucagon-like peptide 1 agonists stimulate expression of homeodomain protein IDX-1 and increase islet size in mouse pancreas
    Stoffers, DA
    Kieffer, TJ
    Hussain, MA
    Drucker, DJ
    Bonner-Weir, S
    Habener, JF
    Egan, JM
    [J]. DIABETES, 2000, 49 (05) : 741 - 748
  • [43] Homeodomain protein IDX-1 - A master regulator of pancreas development and insulin gene expression
    Stoffers, DA
    Thomas, MK
    Habener, JF
    [J]. TRENDS IN ENDOCRINOLOGY AND METABOLISM, 1997, 8 (04) : 145 - 151
  • [44] TEITELMAN G, 1993, DEVELOPMENT, V118, P1031
  • [45] Isolation of multipotent adult stem cells from the dermis of mammalian skin
    Toma, JG
    Akhavan, M
    Fernandes, KJL
    Barnabé-Heider, F
    Sadikot, A
    Kaplan, DR
    Miller, FD
    [J]. NATURE CELL BIOLOGY, 2001, 3 (09) : 778 - 784
  • [46] Pdx1 level defines pancreatic gene expression pattern and cell lineage differentiation
    Wang, HY
    Maechler, P
    Ritz-Laser, B
    Hagenfeldt, KA
    Ishihara, H
    Philippe, J
    Wollheim, CB
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 2001, 276 (27) : 25279 - 25286
  • [47] GLUCAGON-LIKE PEPTIDE-I (7-37) ACTIONS ON ENDOCRINE PANCREAS
    WEIR, GC
    MOJSOV, S
    HENDRICK, GK
    HABENER, JF
    [J]. DIABETES, 1989, 38 (03) : 338 - 342
  • [48] Exendin-4 stimulates both β-cell replication and neogenesis, resulting in increased β-cell mass and improved glucose tolerance in diabetic rats
    Xu, G
    Stoffers, DA
    Habener, JF
    Bonner-Weir, S
    [J]. DIABETES, 1999, 48 (12) : 2270 - 2276
  • [49] Glucagon-like peptide 1 and exendin-4 convert pancreatic AR42J cells into glucagon- and insulin-producing cells
    Zhou, J
    Wang, XL
    Pineyro, MA
    Egan, JM
    [J]. DIABETES, 1999, 48 (12) : 2358 - 2366
  • [50] Multipotential nestin-positive stem cells isolated from adult pancreatic islets differentiate ex vivo into pancreatic endocrine, exocrine, and hepatic phenotypes
    Zulewski, H
    Abraham, EJ
    Gerlach, MJ
    Daniel, PB
    Moritz, W
    Müller, B
    Vallejo, M
    Thomas, MK
    Habener, JF
    [J]. DIABETES, 2001, 50 (03) : 521 - 533