Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Review
. 2015 Dec 30;17(1):48.
doi: 10.3390/ijms17010048.

Notch Signaling in Pancreatic Development

Affiliations
Review

Notch Signaling in Pancreatic Development

Xu-Yan Li et al. Int J Mol Sci. .

Abstract

The Notch signaling pathway plays a significant role in embryonic cell fate determination and adult tissue homeostasis. Various studies have demonstrated the deep involvement of Notch signaling in the development of the pancreas and the lateral inhibition of Notch signaling in pancreatic progenitor differentiation and maintenance. The targeted inactivation of the Notch pathway components promotes premature differentiation of the endocrine pancreas. However, there is still the contrary opinion that Notch signaling specifies the endocrine lineage. Here, we review the current knowledge of the Notch signaling pathway in pancreatic development and its crosstalk with the Wingless and INT-1 (Wnt) and fibroblast growth factor (FGF) pathways.

Keywords: Notch signaling; differentiation; maintenance; pancreatic progenitor.

PubMed Disclaimer

Figures

Figure 1
Figure 1
A schematic of pancreatic development.
Figure 2
Figure 2
A schematic of Notch signaling during pancreatic development. Notch signaling is initiated by the binding of the ligands and receptors of two neighboring cells. Upon activation, Notch is cleaved, releasing the Notch intracellular domain (NICD). The NICD can subsequently translocate into the nucleus to transcriptionally activate Notch target genes. Hes1 inhibits the expression of Ngn3 by blocking its promoter activity.
Figure 3
Figure 3
Notch-mediated lateral inhibition in pancreatic multipotent progenitor cell differentiation.
Figure 4
Figure 4
Notch signaling in the proliferation of pancreatic multipotent progenitor cells.
Figure 5
Figure 5
Inhibitory crosstalk between the Wingless and INT-1 (Wnt) and Notch pathways in pancreatic progenitor cells. The dashed lines signify that the mechanisms existing in the pancreas are unknown. The arrows represent activation whereas bar-headed lines represent inhibition.
Figure 6
Figure 6
The crosstalk between the fibroblast growth factor (FGF) and Notch pathways in pancreatic progenitors. The dashed lines signify that the mechanisms existing in the pancreas are unknown. The arrows represent activation whereas bar-headed lines represent inhibition.

Similar articles

Cited by

References

    1. Artavanis-Tsakonas S., Matsuno K., Fortini M.E. Notch signaling. Science. 1995;268:225–232. doi: 10.1126/science.7716513. - DOI - PubMed
    1. Bray S. Notch signalling in drosophila: Three ways to use a pathway. Semin. Cell Dev. Biol. 1998;9:591–597. doi: 10.1006/scdb.1998.0262. - DOI - PubMed
    1. Buono K.D., Robinson G.W., Martin C., Shi S., Stanley P., Tanigaki K., Honjo T., Hennighausen L. The canonical Notch/Rbp-j signaling pathway controls the balance of cell lineages in mammary epithelium during pregnancy. Dev. Biol. 2006;293:565–580. doi: 10.1016/j.ydbio.2006.02.043. - DOI - PubMed
    1. Kopan R., Ilagan M.X. The canonical Notch signaling pathway: Unfolding the activation mechanism. Cell. 2009;137:216–233. doi: 10.1016/j.cell.2009.03.045. - DOI - PMC - PubMed
    1. Yugawa T., Nishino K., Ohno S., Nakahara T., Fujita M., Goshima N., Umezawa A., Kiyono T. Noncanonical Notch signaling limits self-renewal of human epithelial and induced pluripotent stem cells through rock activation. Mol. Cell. Biol. 2013;33:4434–4447. doi: 10.1128/MCB.00577-13. - DOI - PMC - PubMed

Publication types

LinkOut - more resources