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Gene regulatory factors in pancreatic development

Journal

DEVELOPMENTAL DYNAMICS
Volume 229, Issue 1, Pages 176-200

Publisher

WILEY
DOI: 10.1002/dvdy.10460

Keywords

islet; Hes1; Ngn3; Pdx1; Nkx6.1; Nkx2.2; Ptf1a; Notch; pancreas; endoderm

Funding

  1. NIDDK NIH HHS [P30 DK57516, DK61248-03] Funding Source: Medline
  2. NATIONAL INSTITUTE OF DIABETES AND DIGESTIVE AND KIDNEY DISEASES [U19DK061248, P30DK057516] Funding Source: NIH RePORTER

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The intensity of research on pancreatic development has increased markedly in the past 5 years, primarily for two reasons: we now know that the insulin-producing beta-cells normally arise from an endodermally derived, pancreas-specified precursor cell, and successful transplants of islet cells have been performed, relieving patients with type I diabetes of symptoms for extended periods after transplantation. Combining in vitro beta-cell formation from a pancreatic biopsy of a diabetic patient or from other stem-cell sources followed by endocrine cell transplantation may be the most beneficial route for a future diabetes therapy. However, to achieve this, a thorough understanding of the genetic components regulating the development of beta-cells is required. The following review discusses our current understanding of the transcription factor networks necessary for pancreatic development and how several genetic interactions coming into play at the earliest stages of endodermal development gradually help to build the pancreatic organ. (C) 2003 Wiley-Liss, Inc.

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