Regulation of IGF-1 but not TGF-β1 by NGF in the smooth muscle of the inflamed urinary bladder.

Abstract

Intraperitoneal injection of cyclophosphamide (CYP) causes hemorrhagic cystitis with excess growth of muscular layer leading to bladder hypertrophy; this could be attributable to changes in the expression profiles of growth factors in the inflamed urinary bladder. The growth factors characterized in the current study include nerve growth factor (NGF), insulin-like growth factor (IGF)-1, and transforming growth factor (TGF)-β1. We found that following CYP injection for 8 h and 48 h, the mRNA levels of all three factors were increased in the inflamed bladder when compared to control. The level of NGF mRNA was mainly increased in the urothelium layer while the levels of IGF-1 mRNA and TGF-β1 mRNA were increased in the smooth muscle layer. The level of NGF high affinity receptor TrkA mRNA was also increased in both the urothelium and the smooth muscle layers during bladder inflammation. When we blocked NGF action with NGF neutralizing antibody in vivo, we found that the up-regulation of IGF-1 in the inflamed bladder was reversed while the up-regulation of TGF-β1 was not affected by NGF neutralization. The effect of NGF on regulating IGF-1 expression was further confirmed in bladder smooth muscle culture showing that exogenous NGF increased the mRNA level of IGF-1 after 30 min to 1 h stimulation. These results suggested that bladder inflammation induced region-specific changes in the expression profiles of NGF, IGF-1 and TGF-β1. The up-regulation of NGF in the urothelium may have a role in affecting bladder smooth muscle cell physiology by regulating IGF-1 expression.

• Authors: Qing L Zhang, Li-Ya Qiao
• Journal: Regulatory peptides (Regul Pept) Vol. 177 Issue 1-3 Pg. 73-8 (Aug 20 2012) ISSN: 1873-1686 [Electronic] Netherlands
• PMID: 22579999 (Publication Type: Journal Article, Research Support, N.I.H., Extramural)
• Copyright: Published by Elsevier B.V.

Chemical References

• Antibodies, Neutralizing
• RNA, Messenger
• Tgfb1 protein, rat
• Transforming Growth Factor beta1
• insulin-like growth factor-1, rat
• Insulin-Like Growth Factor I
• Cyclophosphamide
• Nerve Growth Factor
• Receptor, trkA

Topics

• Animals
• Antibodies, Neutralizing (metabolism)
• Cells, Cultured
• Cyclophosphamide (administration & dosage, pharmacology)
• Cystitis (chemically induced, metabolism, pathology)
• Gene Expression Regulation
• Insulin-Like Growth Factor I (genetics, metabolism)
• Male
• Muscle, Smooth (drug effects, metabolism, pathology)
• Nerve Growth Factor (metabolism, pharmacology)
• RNA, Messenger (metabolism)
• Rats
• Rats, Sprague-Dawley
• Receptor, trkA (genetics, metabolism)
• Time Factors
• Transforming Growth Factor beta1 (genetics, metabolism)
• Up-Regulation
• Urinary Bladder (drug effects, metabolism, pathology)
• Urothelium (drug effects, metabolism, pathology)