A conserved role for retinoid signaling in vertebrate pancreas development

被引:77
作者
Stafford, D
Hornbruch, A
Mueller, PR
Prince, VE
机构
[1] Univ Chicago, Dept Organismal Biol & Anat, Chicago, IL 60637 USA
[2] Univ Chicago, Ctr Mol Oncol, Comm Dev Biol, Chicago, IL 60637 USA
[3] Univ Chicago, Dept Mol Genet & Cell Biol, Chicago, IL 60637 USA
[4] Univ Chicago, Ctr Mol Oncol, Comm Canc Biol, Chicago, IL 60637 USA
[5] Univ Chicago, Ctr Mol Oncol, Comm Genet, Chicago, IL 60637 USA
[6] Univ Chicago, Comm Neurobiol, Chicago, IL 60637 USA
[7] Univ Chicago, Comm Evolutionary Biol, Chicago, IL 60637 USA
关键词
pancreas; liver; Xenopus; quail; retinoic acid;
D O I
10.1007/s00427-004-0420-6
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Retinoic acid (RA) signaling plays critical roles in the regionalization of the central nervous system and mesoderm of all vertebrates that have been examined. However, to date, a role for RA in pancreas and liver development has only been demonstrated for the teleost zebrafish. Here, we demonstrate that RA signaling is required for development of the pancreas but not the liver in the amphibian Xenopus laevis and the avian quail. We disrupted RA signaling in Xenopus tadpoles, using both a pharmacological and a dominant-negative strategy. RA-deficient quail embryos were obtained from hens with a dietary deficiency in vitamin A. In both species we found that pancreas development was dependent on RA signaling. Furthermore, treatment of Xenopus tadpoles with exogenous RA led to an expansion of the pancreatic field. By contrast, liver development was not perturbed by manipulation of RA signaling. Taken together with our previous finding that RA signaling is necessary and sufficient for zebrafish pancreas development, these data support the hypothesis that a critical role for RA signaling in pancreas development is a conserved feature of the vertebrates.
引用
收藏
页码:432 / 441
页数:10
相关论文
共 41 条
  • [21] Vitamin A-deficient quail embryos have half a hindbrain and other neural defects
    Maden, M
    Gale, E
    Kostetskii, I
    Zile, M
    [J]. CURRENT BIOLOGY, 1996, 6 (04) : 417 - 426
  • [22] Conservation of PDX-1 structure, function, and expression in zebrafish
    Milewski, WM
    Duguay, SJ
    Chan, SJ
    Steiner, DF
    [J]. ENDOCRINOLOGY, 1998, 139 (03) : 1440 - 1449
  • [23] Moriya N, 2000, DEV GROWTH DIFFER, V42, P175
  • [24] Niederreither K, 2000, DEVELOPMENT, V127, P75
  • [25] Niederreither K, 2002, DEVELOPMENT, V129, P3563
  • [26] Nieuwkoop P.D., 1994, NORMAL TABLE XENOPUS, DOI 10.1201/9781003064565-29
  • [27] Offield MF, 1996, DEVELOPMENT, V122, P983
  • [28] IPF1, A HOMEODOMAIN-CONTAINING TRANSACTIVATOR OF THE INSULIN GENE
    OHLSSON, H
    KARLSSON, K
    EDLUND, T
    [J]. EMBO JOURNAL, 1993, 12 (11) : 4251 - 4259
  • [29] Deficits in the posterior pharyngeal endoderm in the absence of retinoids
    Quinlan, R
    Gale, E
    Maden, M
    Graham, A
    [J]. DEVELOPMENTAL DYNAMICS, 2002, 225 (01) : 54 - 60
  • [30] Hedgehog signaling pathway is essential for pancreas specification in the zebrafish embryo
    Roy, S
    Qiao, T
    Wolff, C
    Ingham, PW
    [J]. CURRENT BIOLOGY, 2001, 11 (17) : 1358 - 1363