The production of nerve growth factor by human bladder smooth muscle cells in vivo and in vitro

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Abstract
Objective To measure the concentrations of nerve growth factor (NGF) in tissue biopsies taken from subjects with a normal bladder and from patients diagnosed to have idiopathic detrusor instability (associated with a reduction in the density of motor nerves), and to use anin vitromodel to study the mechanisms of NGF expression.Materials and methods Biopsy specimens were obtained during endoscopic and open surgery from patients undergoing routine bladder surgery. The patients were divided into two categories based upon urodynamic characterization. The NGF content in samples from 11 normal bladders and seven idiopathic unstable bladders were measured using an enzyme‐linked immunosorbent assay. The mechanisms influencing net NGF production were explored using detrusor cellsin vitro.Results The mean (sem) NGF content was significantly higher in unstable tissues, at 0.96 (0.05) pg/µg protein, than in the normal bladder, at 0.53 (0.05) pg/µg protein. In the cell model, acetylcholine (10 µmol/L), noradrenaline (1 and 10 µmol/L) and ATP (1 µmol/L) caused a significant increase in net NGF production; acetylcholine at 1 µmol/L had no effect. Direct stimulation of protein kinase C (PKC) by phorbol ester (33 ng/mL) or elevation of cAMP using forskolin (10 µmol/L) increased NGF, suggesting that at least two intracellular pathways (PKC‐ and PKA‐dependent) are involved. The expression ofc‐Foswas increased by phorbol 12‐myristate 13‐acetate added before NGF, suggesting thatc‐Fosmay be involved in regulating NGF production.Conclusion These data suggest a role for NGF in the physiology and pathophysiology of the human bladder, and indicate some of the possible mechanisms which might regulate NGF production.