Expression of growth factors and receptors during specific phases in regenerating urothelium after acute injury in vivo
- PMID: 7977650
- PMCID: PMC1887427
Expression of growth factors and receptors during specific phases in regenerating urothelium after acute injury in vivo
Abstract
We investigated the spatio-temporal changes in RNA and protein expression of growth factors and their receptors by in situ hybridization and immunocytochemistry during regeneration after acute injury of mouse urothelium in vivo. These data were correlated with changes in morphology and proliferation during regeneration. Except for an enhanced muscular transforming growth factor-beta 1 (TGF-beta 1) and TGF-beta type II receptor expression, changes in expression patterns of growth factors or receptors were confined to the urothelium. Increased mucosal RNA expression of insulin-like growth factor-II (IGF-II) and particularly of type I IGF receptor, as well as fibroblast growth factor-1 (FGF-1) but not of FGF-2, coincided with re-epithelialization and urothelial proliferation. Both high levels of urothelial TGF-beta 1 RNA and protein expression were associated with re-epithelialization and differentiation. In addition, TGF beta type II receptor protein expression was similarly enhanced in the same urothelial cells. Platelet-derived growth factor-A (PDGF-A) RNA was expressed constitutively in the mucosa but decreased in the reepithelialization phase. The data are consistent with the notion that urothelial regeneration can be achieved by paracrine or autocrine acting, urothelium-derived growth factors. Since analogous growth factor RNA expression patterns in regenerating skin epidermis have been found, a more general growth factor-regulated mechanism for epithelial regeneration may be suggested.
Similar articles
-
Functions of fibroblast and transforming growth factors in primary organoid-like cultures of normal human urothelium.Lab Invest. 1996 Aug;75(2):147-56. Lab Invest. 1996. PMID: 8765315
-
Expression of growth factors, growth inhibiting factors, and their receptors in invasive breast cancer. I: An inventory in search of autocrine and paracrine loops.J Pathol. 1998 Jan;184(1):44-52. doi: 10.1002/(SICI)1096-9896(199801)184:1<44::AID-PATH984>3.0.CO;2-H. J Pathol. 1998. PMID: 9582526
-
Expression of growth factors, growth-inhibiting factors, and their receptors in invasive breast cancer. II: Correlations with proliferation and angiogenesis.J Pathol. 1998 Jan;184(1):53-7. doi: 10.1002/(SICI)1096-9896(199801)184:1<53::AID-PATH6>3.0.CO;2-7. J Pathol. 1998. PMID: 9582527
-
Growth factors in renal development.Semin Nephrol. 1995 Jul;15(4):291-9. Semin Nephrol. 1995. PMID: 7569409 Review.
-
Cellular signaling in the bladder.Front Biosci. 1997 Dec 1;2:d592-5. doi: 10.2741/a215. Front Biosci. 1997. PMID: 9374449 Review.
Cited by
-
Amitriptyline aggravates the fibrosis process in a rat model of infravesical obstruction.Int J Exp Pathol. 2012 Jun;93(3):218-24. doi: 10.1111/j.1365-2613.2012.00813.x. Epub 2012 May 8. Int J Exp Pathol. 2012. PMID: 22563623 Free PMC article.
-
The Urothelium: Life in a Liquid Environment.Physiol Rev. 2020 Oct 1;100(4):1621-1705. doi: 10.1152/physrev.00041.2019. Epub 2020 Mar 19. Physiol Rev. 2020. PMID: 32191559 Free PMC article. Review.
-
Loss of β1-integrin from urothelium results in overactive bladder and incontinence in mice: a mechanosensory rather than structural phenotype.FASEB J. 2013 May;27(5):1950-61. doi: 10.1096/fj.12-223404. Epub 2013 Feb 8. FASEB J. 2013. PMID: 23395910 Free PMC article.
-
Wound healing responses of urinary extravasation after urethral injury.Sci Rep. 2023 Jun 30;13(1):10628. doi: 10.1038/s41598-023-37610-2. Sci Rep. 2023. PMID: 37391520 Free PMC article.
-
The morphological regeneration and functional restoration of bladder defects by a novel scaffold and adipose-derived stem cells in a rat augmentation model.Stem Cell Res Ther. 2017 Jun 24;8(1):149. doi: 10.1186/s13287-017-0597-z. Stem Cell Res Ther. 2017. PMID: 28646909 Free PMC article.
References
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Other Literature Sources