scholarly journals Fibroblast growth factor receptor-3 is expressed in undifferentiated intestinal epithelial cells during murine crypt morphogenesis

2004 ◽  
Vol 230 (1) ◽  
pp. 114-123 ◽  
Author(s):  
Alda Vidrich ◽  
Jenny M. Buzan ◽  
Chibuzo Ilo ◽  
Leigh Bradley ◽  
Kirstin Skaar ◽  
...  
Keyword(s):  
Growth Factor ◽  
Epithelial Cells ◽  
Fibroblast Growth Factor ◽  
Fibroblast Growth Factor Receptor ◽  
Intestinal Epithelial Cells ◽  
Growth Factor Receptor ◽  
Intestinal Epithelial ◽  
Fibroblast Growth

Up-regulation of Fibroblast Growth Factor Receptor-1 in Lens Epithelial Cells Paralleled by Growth Stimulation

1998 ◽  
Vol 67 (5) ◽  
pp. 611-616 ◽  
Author(s):  
TOHRU MARUNOUCHI ◽  
HIROMI HOSOYA ◽  
TOSHIE MORIOKU ◽  
TAKAYUKI MORI ◽  
YOSHINAO MAJIMA ◽  
...  
Keyword(s):  
Growth Factor ◽  
Epithelial Cells ◽  
Fibroblast Growth Factor ◽  
Fibroblast Growth Factor Receptor ◽  
Growth Factor Receptor ◽  
Growth Stimulation ◽  
Lens Epithelial Cells ◽  
Fibroblast Growth

Intestinal epithelial cells proliferate in response to fibroblast growth factor 10

2006 ◽  
Vol 130 (2) ◽  
pp. 178-179
Author(s):  
J.L. Curtis ◽  
A. Grishin ◽  
P.M. Del Moral ◽  
F.G. Sala ◽  
L. Lee ◽  
...  
Keyword(s):  
Growth Factor ◽  
Epithelial Cells ◽  
Fibroblast Growth Factor ◽  
Intestinal Epithelial Cells ◽  
Intestinal Epithelial ◽  
Fibroblast Growth ◽  
Fibroblast Growth Factor 10

scholarly journals A Stem Structure in Fibroblast Growth Factor Receptor 2 Transcripts Mediates Cell-Type-Specific Splicing by Approximating Intronic Control Elements

2003 ◽  
Vol 23 (24) ◽  
pp. 9327-9337 ◽  
Author(s):  
Andrew P. Baraniak ◽  
Erika L. Lasda ◽  
Eric J. Wagner ◽  
Mariano A. Garcia-Blanco
Keyword(s):  
Alternative Splicing ◽  
Growth Factor ◽  
Epithelial Cells ◽  
Fibroblast Growth Factor ◽  
Fibroblast Growth Factor Receptor ◽  
Growth Factor Receptor ◽  
Fibroblast Growth ◽  
Cell Type ◽  
Cell Type Specific ◽  
Stem Structure

ABSTRACT Alternative splicing of fibroblast growth factor receptor 2 (FGFR2) occurs in a cell-type-specific manner with the mutually exclusive use of exon IIIb or exon IIIc. Specific inclusion of exon IIIb is observed in epithelial cells, whereas exon IIIc inclusion is seen in mesenchymal cells. Epithelium-specific activation of exon IIIb and repression of exon IIIc are coordinately regulated by intronic activating sequence 2 (IAS2) and intronic splicing activator and repressor (ISAR) elements in FGFR2 pre-mRNA. Previously, it has been suggested that IAS2 and a 20-nucleotide core sequence of ISAR form a stem structure that allows for the proper regulation of FGFR2 alternative splicing. Replacement of IAS2 and the ISAR core with random sequences capable of stem formation resulted in the proper activation of exon IIIb and repression of exon IIIc in epithelial cells. Given the high degree of phylogenetic conservation of the IAS2-ISAR core structure and the fact that unrelated stem-forming sequences could functionally substitute for IAS2 and ISAR elements, we postulated that the stem structure facilitated the approximation of intronic control elements. Indeed, deletion of the entire stem-loop region and juxtaposition of sequences immediately upstream of IAS2 with sequences immediately downstream of the ISAR core maintained proper cell-type-specific inclusion of exon IIIb. These data demonstrate that IAS2 and the ISAR core are dispensable for the cell-type-specific activation of exon IIIb; thus, the major, if not the sole, role of the IAS2-ISAR stem in exon IIIb activation is to approximate sequences upstream of IAS2 with sequences downstream of the ISAR core. The downstream sequence is very likely a highly conserved GCAUG element, which we show was required for efficient exon IIIb activation.

Cytokine regulation of fibroblast growth factor receptor 3 IIIb in intestinal epithelial cells

1997 ◽  
Vol 272 (4) ◽  
pp. G885-G893 ◽  
Author(s):  
M. Kanai ◽  
I. Rosenberg ◽  
D. K. Podolsky
Keyword(s):  
Growth Factors ◽  
Growth Factor ◽  
Epithelial Cells ◽  
Fibroblast Growth Factor ◽  
Transforming Growth Factor ◽  
Intestinal Epithelial Cells ◽  
Interleukin 2 ◽  
Intestinal Epithelial ◽  
Fibroblast Growth ◽  
Fgf Receptor

Proliferation and function of the intestinal epithelium is modulated by a range of regulatory peptides, including cytokines and peptide growth factors. To define mechanisms integrating these regulatory systems, the effects of growth factors and cytokines on the expression of the fibroblast growth factor (FGF) receptor 3 (FGFR3) IIIb expressed on intestinal epithelial cells were examined in Caco-2 cells. Regulated expression of FGFR3 IIIb was associated with acquisition of the differentiated state. Keratinocyte growth factor (KGF), a ligand of another member of the FGF receptor family, enhanced expression of FGFR3 IIIb, but acidic FGF, the ligand for FGFR3 IIIb itself, had no effect. Epidermal growth factor and transforming growth factor-beta also markedly enhanced FGFR3 IIIb expression in a different temporal pattern. In addition, FGFR3 IIIb expression was increased 10-fold by the cytokine interleukin-2. These studies demonstrate integration between cytokines and growth factor ligand-receptor systems in intestinal epithelial cells.

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