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Published on: October 30, 2013
Do we understand any more about bladder interstitial cells?-ICI-RS 2013
Anthony Kanai1, Christopher Fry, Ann Hanna-Mitchell
1University of Pittsburgh, Pittsburgh, Pennsylvania.
Insights
Interstitial cells (ICs) in the lower urinary tract play a role in bladder function and pathology. While much is known, their precise physiological roles and mechanisms require further investigation.
Area of Science:
- Urology
- Cell Biology
- Physiology
Background:
- Interstitial cells (ICs) are crucial components of the lower urinary tract.
- Their characterization is often based on comparisons with interstitial cells of Cajal in the gastrointestinal tract.
Purpose of the Study:
- To review discussions on lower urinary tract interstitial cells from the 2013 International Consultation on Incontinence-Research Society (ICI-RS) meeting.
- To explore current understanding of IC subtypes, localization, and communication within the bladder.
Main Methods:
- Discussion focused on IC subtypes, localization, and intercellular communication.
- The role of ICs in bladder pathologies and novel research methodologies were also addressed.
Main Results:
- ICs are believed to drive intrinsic contractions in fetal bladders, diminishing postpartum.
- Post-spinal cord injury, enhanced IC activity may contribute to neurogenic detrusor overactivity and incontinence.
- IC-mediated activity appears initiated by urothelial factors and may involve gap junction coupling.
Conclusions:
- Significant information has been gathered on bladder ICs.
- However, many pathophysiological functions and underlying mechanisms remain unclear.
- Further research is essential to fully elucidate the role of ICs in lower urinary tract function and dysfunction.
Aims:
To present a brief review on discussions from "Do we understand any more about lower urinary tract interstitial cells?" session at the 2013 International Consultation on Incontinence-Research Society (ICI-RS) meeting in Bristol, UK.
Methods:
Discussion focused on bladder interstitial cell (IC) subtypes, their localization and characterization, and communication between themselves, the urothelium, and detrusor smooth muscle. The role of ICs in bladder pathologies and new methods for studying ICs were also addressed.
Results:
ICs have been studied extensively in the lower urinary tract and have been characterized based on comparisons with ICs of Cajal in the gastro-intestinal tract. In fetal bladders it is believed that ICs drive intrinsic contractions to expel urine through the urachus. These contractions diminish postpartum as bladder innervation develops. Voiding in human neonates occurs when filling triggers a spinal cord reflex that contracts the detrusor; in rodents, maternal stimulation of the perineum triggers voiding. Following spinal cord injury, intrinsic contractions, and spinal micturition reflexes develop, similar to those seen during neonatal development. These enhanced contractions may stimulate nociceptive and mechanosensitive afferents contributing to neurogenic detrusor overactivity and incontinence. The IC-mediated activity is believed to be initiated in the lamina propria by responding to urothelial factors. These IC may act syncytially through gap junction coupling and modulate detrusor activity through unknown mechanisms.
Conclusion:
There has been a great deal of information discovered regarding bladder ICs, however, many of their (patho)physiological functions and mechanisms are still unclear and necessitates further research. Neurourol. Urodynam. 33:573-576, 2014. © 2014 Wiley Periodicals, Inc.
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