|Home | About | Journals | Submit | Contact Us | Français|
Although the urinary bladder urothelium has classically been thought of as a passive barrier to ions and solutes, a number of novel properties have been recently attributed to urothelial cells. Studies have revealed that the urothelium is involved in sensory mechanisms (i.e. the ability to express a number of sensor molecules or respond to thermal, mechanical and chemical stimuli) and can release chemical mediators. Localization of afferent nerves next to the urothelium suggests that urothelial cells could be targets for neurotransmitters released from bladder nerves or that chemicals released by urothelial cells could alter afferent nerve excitability. Taken together, these and other findings highlighted in this article suggest a sensory function for the urothelium. Elucidation of mechanisms that influence urothelial function might provide insights into the pathology of bladder dysfunction.
The urothelium is the epithelial lining of the urinary tract between the renal pelvis and the urinary bladder. Urothelium is composed of at least three layers: a basal cell layer attached to a basement membrane, an intermediate layer, and a superficial or apical layer composed of large hexagonal cells (diameters of 25–250 μm) known as ‘umbrella cells’.1,2 The umbrella cells are interconnected by tight junctions and are covered on their apical surface by crystalline proteins called uroplakins which assemble into hexagonal plaques.1–4 Uroplakins and other urothelial cellular differentiation markers, such as cyto keratin 20, are not expressed in the stratified epithelium of the urethra.5 In some species, the umbrella cells and perhaps also the intermediate cells have projections to the basement membrane.1,6,7 The barrier function of the urothelium is dependent on several features of the umbrella cell layer: these features include tight-junction complexes that reduce the movement of ions and solutes between cells, and specialized lipid molecules and uroplakin proteins in the apical membrane, which reduce the permeability of the cells to small molecules (e.g. water, urea, protons).1,2,8,9 The apical surface of the urothelium is also covered with a sulfated poly saccharide glycosaminoglycan layer that is thought to act as a nonspecific anti-adherence factor and as a defense mechanism against infection.5,10
Basal cells, which are thought to be precursors for other cell types, normally exhibit a low (3–6 months) turnover rate, which is in fact the slowest turnover of any mammalian epithelial cells. It has been shown that neither urine-derived factors nor cyclic mechanical changes contribute to the maintenance of urothelial differentiation; however, accelerated proliferation can occur in pathologic conditions.11 For example, when protamine sulfate was used to damage selectively only the umbrella cell layer, it was shown that the urothelium rapidly undergoes both functional and structural changes in order to restore the barrier. The initiation of urothelial proliferation is thought to involve upregulation of growth factors. such as fibroblast growth factor and nerve growth factor.12,13
Although the urothelium maintains a tight barrier to ion and solute flux, a number of local factors (e.g. tissue pH, mechanical or chemical trauma, and bacterial infection) can modulate the barrier function of the urothelium.7,14 Other conditions, such as interstitial cystitis or spinal cord injury can also change the urothelial barrier.15,16 When the barrier is compromised, water, urea and toxic substances can pass into the underlying tissue (neural and/or muscle layers), which results in symptoms of urgency, frequency and pain during bladder filling and voiding. In some pathologic conditions, disruption of the urothelial barrier is associated with ultrastructural changes and alterations in the levels of chemical mediators such as nitric oxide (NO) and ATP which can alter epithelial function and/or integrity.15,16 Disruption of urothelial barrier integrity has also been linked to the expression of substances such as antiproliferative factor, which has been detected in the urine of patients with interstitial cystitis, and has been shown to be secreted by bladder epithelial cells obtained from these patients. Antiproliferative factor can inhibit epithelial proliferation, which adversely affects barrier function.17,18
Urinary tract infections with uropathogenic Escherichia coli (UPEC) are initiated by bacterial adherence to uroplakin proteins on the apical surface of umbrella cells.14,19 Adherence is followed by bacterial invasion of the bladder wall. Internalization of UPEC in the umbrella cells and formation of intracellular colonies (biofilm-like pods) of UPEC in umbrella cells has been implicated in the mechanism of chronic urinary tract infection.19
Disruption of urothelial function by distant pathologic conditions is thought to be mediated by neural or hormonal mechanisms. For example, spinal-cord transection in rats leads to a rapid alteration in the urothelial barrier, including ultrastructural changes and increased permeability.15 These changes were prevented by administration of a ganglionic blocking agent before spinal-cord transection, which indicated that efferent autonomic pathways are involved in the acute effects of spinal-cord injury on bladder urothelium. Other types of urothelial–neural interactions are also likely; various stimuli have been reported to induce urothelial cells to release chemical mediators that can, in turn, modulate the activity of afferent nerves.1,20,21 These findings have raised the possibility that the urothelium could have a role in sensory mechanisms in the urinary tract.
In summary, modification of the urothelium and/or loss of epithelial integrity in a number of pathologic conditions can result in the passage of toxic and irritating urinary constituents through the urothelium, or release of neuroactive substances from the urothelium, which leads to changes in the properties of sensory nerves and sensory symptoms such as urinary frequency and urgency. Chemical communication between the nervous system and urothelial cells might, therefore, have an important role in the generation of urinary bladder dysfunction.
Studies have shown that both afferent and autonomic efferent nerves are located in close proximity to the urothelium (Figure 1).20–24 Peptide-immunoreactive and TRPV1-immunoreactive nerve fibers that are presumed to be afferent nerves are localized throughout the urinary bladder musculature and in a plexus that lies beneath, and extends into, the urothelium.20,21 Markers for cholinergic and adrenergic nerves have also been detected in these same regions. The anatomic substrate for bidirectional urothelial–neural communication exists in the urinary bladder. In addition, a layer of cells with morphologic properties similar to those of myofibroblasts has been detected in the sub urothelial space of the bladder in both humans and animals (Figure 1).25–27 These cells (which also make close contact with nerves) can release and be activated by ATP and, therefore, could act as an intermediary in urothelium–afferent nerve interactions.
While the urothelium has been historically viewed primarily as a barrier, it is increasingly recognized to be a responsive structure that is capable of detecting physiological and chemical stimuli, and of releasing a number of signaling molecules (Figure 1). Several substances are released from urothelial cells following physical and chemical stimulation: ATP; NO; substance P; acetylcholine, adenosine, antiproliferative factor, cytokines, prostanoids and various trophic factors. Data accumulated over several years indicate that urothelial cells display a number of properties similar to those of sensory neurons such as nociceptors and mechanoreceptors (Figure 1), and that both types of cells use diverse signal-transduction mechanisms to detect physiological stimuli.
Examples of neuronal ‘sensor molecules’ (i.e. receptors and ion channels) that have been identified in the urothelium include receptors for bradykinin, neurotrophins (Trk-A and p75), purines (P2X and P2Y), norepinephrine (α and β), acetylcholine (nicotinic and muscarinic receptors), protease-activated receptors, amiloride-sensitive and mechanosensitive Na+ channels, and a number of transient receptor potential (TRP) channels (TRPV1, TRPV2, TRPV4, TRPM8) (Table 1).28–38
Since the first report (in 1997) of distension-evoked ATP release from bladder urothelium, evidence that supports a role for urothelial-derived ATP release in both autocrine and paracrine signaling in the bladder has emerged.33 P2X and P2Y purinergic receptor subtypes are expressed in cells (urothelium, nerves and myofibroblasts) that are located at or near the luminal surface of the bladder, which suggests that ATP has an important role in chemical communication in the bladder. Basolateral ATP release from urothelial cells following either chemical or mechanical stimuli21,29,32 might signal to adjacent urothelial cells as well as to other cell types (myofibroblasts or bladder nerves) within the submucosa (Figure 1). In addition, the close proximity of urothelial cells to myofibroblasts and bladder nerves, the sensitivity of these cells to ATP (indicated by an ATP-induced increase in intracellular Ca2+ in afferent neurons, urothelial cells and myofibroblasts), and the evidence for cell–cell coupling mediated by gap junctions provide support for a number of physical and chemical interactions that could influence bladder function.25,39 Activation of P2Y or P2X receptors by ATP release during bladder distension could, therefore, have a role in autocrine and paracrine signaling throughout the urothelium. This hypothesis is supported by a study published in 2005, which found that urothelial-derived ATP release in the urinary bladder purportedly acts as a trigger for exocytosis—in part via autocrine activation of urothelial purinergic (P2X and P2Y) receptors.40
By activation of a population of suburothelial bladder afferent nerves that express P2X3 or P2X2 receptors, ATP released from urothelial cells during bladder distension could trigger sensations of fullness and pain, or induce reflex changes in bladder activity.30 This concept receives support from studies in P2X3 null mice which exhibited urinary bladder hyporeflexia.41 By contrast, clinical studies showed that patients who exhibited neurogenic detrusor over-activity have increased P2X3 immuno reactive suburothelial innervation.42 Taken together, these data suggest that purinergic receptors and neural–epithelial interactions are essential for normal bladder function.
In the last 5 years, various studies have shown that pathology often results in augmented ATP release from the urothelium, which can cause painful sensations by excitation of purinergic (P2X) receptors on sensory fibers.29,30,43 There is speculation that this type of noncholinergic mechanism could have a role in a number of bladder pathologies (e.g. idiopathic detrusor instability, interstitial cystitis and bladder-outflow obstruction), as well as in the aging bladder.44,45 In 2001, it has been shown in sensory neurons that ATP can potentiate the response of vanilloids (by lowering the threshold for protons, capsaicin and heat).46 This novel mechanism represents a means by which large amounts of ATP released from damaged or sensitized cells, in response to injury or inflammation, are thought to trigger the sensation of pain. These findings have clinical significance; they indicate that alterations to afferent nerves or epithelial cells in pelvic viscera might contribute to the sensory abnormalities observed in a number of pelvic disorders, such as interstitial cystitis—a chronic clinical disease characterized by urgency, frequency and bladder pain upon filling.47–49 Studies of a comparable disease in cats (i.e. feline interstitial cystitis) revealed an augmented stretch-evoked release of urothelium-derived ATP and changes in P2X and P2Y receptor profiles in urothelial cells.29,50,51 This observation is consistent with similar findings in patients with interstitial cystitis.43 These results suggest that urothelial sensor molecules exhibit plasticity in pathologic conditions, and might contribute to bladder pain syndromes.
One example of a urothelial sensor molecule is transient receptor potential cation channel subfamily V member 1 (TRPV1), which is known to have a prominent role in nociception and in urinary bladder function (Figure 2). It is well established that painful sensations induced by capsaicin, the spicy substance in chili peppers, are caused by stimulation of TRPV1.52,53 This ion-channel protein is also activated by moderate heat, protons and lipid metabolites such as anandamide (an endogenous ligand of both cannabinoid and vanilloid receptors). TRPV1 is expressed throughout the afferent limb of the micturition reflex pathway, including in urinary bladder unmyelinated (C-fiber) nerves that detect bladder distension or the presence of irritant chemicals.54,55 In the urinary bladder, one of the more remarkable findings is that TRPV1 is not only expressed by afferent nerves in close contact with urothelial cells, but it is also expressed by urothelial cells (Figure 2).20,21 Activation of urothelial TRPV1 receptors with capsaicin or resiniferatoxin increases levels of intracellular Ca2+ and evokes neurotransmitter (NO or ATP) release in cultured cells. As noted in sensory neurons, these responses are enhanced by low pH, blocked by TRPV1 antagonists, and eliminated in TRPV1-null mice. In neurons, TRPV1 is thought to integrate or amplify the response to various stimuli and, therefore, has an essential role in the development of inflammation-induced hyperalgesia. It seems likely that urothelial TRPV1 might participate in a similar manner in the detection of irritant stimuli following bladder inflammation or infection.
Although TRPV1-null mice are anatomically normal, they exhibit a number of alterations in bladder function, including a reduction of in vitro, stretch-evoked ATP release and membrane capacitance. Urothelial cells cultured from TRPV1-null mice also show a decrease in hypotonic-evoked ATP release.21 These findings demonstrate that the functional significance of TRPV1 in the bladder extends beyond an involvement in pain sensation to include participation in normal voiding functions. TRPV1 is essential for mechanically evoked purinergic signaling by the urothelium.
Intravesical instillation of vanilloids (capsaicin or resiniferatoxin) improves urodynamic parameters in patients with detrusor overactivity. This procedure has been reported to reduce bladder pain in some patients with hypersensitivity disorders, presumably by desensitization of bladder nerves.54,55 This treatment could also target TRPV1 on urothelial cells; persistent activation might lead to receptor desensitization or depletion of urothelial transmitters. Bladder biopsies taken from patients with neurogenic detrusor overactivity showed increased TRPV1 expression in both bladder nerves and the urothelium.8 In these patients, intravesical treatment with resiniferatoxin reduced TRPV1 immunoreactivity in both suburothelial afferent nerve cells and urothelial cells. Parallel changes in TRPV1 expression in both nerves and urothelial cells further support a neuron-like role for the urothelium, and indicate a possible role for TRPV1 in the pathophysiology of the neurogenic bladder.
Patients with overactive bladder are typically treated with muscarinic-receptor antagonists.56,57 These agents prevent the stimulation of postjunctional muscarinic receptors by acetylcholine released from bladder efferent nerves and result in increased bladder capacity. While these agents also target muscarinic receptors on the bladder smooth muscle, evidence that the urothelium expresses the full complement of muscarinic receptors (M1–M5) has sparked an interest in finding out more about the role of the urothelium in the overactive bladder.31,58,59
Since antimuscarinic agents effectively enhance the storage phase of micturition, when parasympathetic nerves are silent, it is postulated that the release of acetylcholine from the urothelium might contribute to detrusor overactivity.60 In addition, release of acetylcholine from nearby bladder efferent nerves could activate urothelial muscarinic receptors. This activation, in turn, could lead to the release of mediators such as ATP that alter bladder sensation by stimulating nearby sensory afferent nerves.29 In addition, distension-evoked release of acetylcholine could target muscarinic receptors on smooth muscle and other cell types, as well as on bladder nerves. Accordingly, targeting muscarinic receptors activated by acetylcholine released from the urothelium and/or other urothelial-release mechanisms may prove to be an effective therapy. In this regard, the use of botulinum toxin has been investigated for treating a number of bladder disorders including neurogenic detrusor overactivity, detrusor-sphincter dyssynergia as well as interstitial cystitis.61–63 The inhibition of muscle contraction is due to the ability to block release of a number of transmitters (ACh; ATP) from bladder nerves by blocking exocytosis.64 However, besides targeting bladder nerves, botulinum toxins have recently been shown to prevent the release of transmitters from bladder urothelium.65
The urothelium expresses both α and β subtypes of adrenergic receptors, which can trigger the release of a number of mediators including ATP and NO.28,66 It is possible that neurally released norepinephrine might have an effect on the urothelium, and might influence bladder function, because of the close proximity of adrenergic nerves that innervate blood vessels in the suburothelial region.22,23,67 Patients with a variety of lower urinary tract disorders including overactive bladder, benign prostatic hyperplasia and even interstitial cystitis—are often treated with selective α1-adrenergic antagonists.68,69 Studies in mice that lack the α1D adrenergic receptor have indicated that there is an important role for these receptors in the regulation of bladder function.70 The α1D adrenergic receptor is expressed within the bladder urothelium, and it seems that tonic activation of urothelial α1D receptors by catecholamines might be involved in bladder sensory mechanisms.71 Catecholamines could be released from nerves adjacent to the urothelium or from nerves that innervate nearby blood vessels, as the suburothelial region receives a rich blood supply. It has been shown that stimulation of both α-adrenergic and β-adrenergic receptors on urothelial cells evokes the release of NO.28,66 It has also been shown that cats diagnosed with feline interstitial cystitis exhibit an increase in norepinephrine content in the urinary bladder, compared with healthy cats.72 In addition, urothelial cells from cats with feline interstitial cystitis exhibit an augmented release of mediators including ATP and NO, which is similar to that observed in human interstitial cystitis.29,73 It is not known whether catecholamines are involved in the increased release of these mediators, or whether a tonic activation of the urothelium via circulating or other sources of catecholamines has a role in the sensory abnormalities of feline interstitial cystitis.
NO is thought to be involved in many functions of the lower urinary tract, ranging from inhibition of neurotransmission in the urethra to modulation of bladder afferent nerves and bladder reflex pathways in the spinal cord.74 The localization of neuronal nitric oxide synthase (NOS) and/or NADPH diaphorase (a marker for neuronal NOS) in efferent and afferent nerve fibers and the expression of multiple NOS isoforms (neuronal, endothelial, and inducible) within the urothelium indicate that NO has a role in the micturition reflex pathway.28,74 The release of NO from the urothelium or other cells is thought to either facilitate or inhibit the activity of bladder afferent nerves. For example, a reduction in NO levels adjacent to the urothelium (caused by intravesical administration of oxyhemoglobin) results in bladder hyperactivity, which suggests that there is an inhibitory role for NO in the control of bladder function.75 Injury or chronic inflammation has been shown to alter the expression of NOS, which raises the possibility that the neurotransmitter function of NO is plastic and can be altered by chronic pathologic conditions.76 For example, intravesical administration of NO donors suppresses the bladder hyperactivity in animals treated with cyclophosphamide.77,78 In addition, it has been reported that NO levels are decreased in patients with interstitial cystitis, a clinical syndrome that is characterized by bladder pain, urinary urgency and frequency.79 Alterations in NO levels could, therefore, affect the excitability of sensory fibers in the urinary bladder. NO might also have a role in epithelial function,80 as a change in NO production or synthesis in intestinal epithelial cells can increase their permeability to hydrophilic macromolecules. This mechanism might contribute to the loss of membrane barrier integrity in many disease states.
Research during the last few years has markedly changed how we view the function of the urothelium. This tissue not only acts as a highly efficient barrier, but also exhibits properties similar to those of nociceptive and mechanoceptive afferent neurons. Activation of urothelial cells by chemical, thermal or mechanical stimuli can evoke the release of various mediators or neurotransmitters that influence neural activity and ultimately bladder function. These observations open new exciting avenues for research in urothelial biology—including pharmacologic interventions that aim to target urothelial receptor and ion channel expression, or neurotransmitter release mechanisms—could lead to new strategies for the clinical management of bladder disorders.
This work was supported by NIH grants to L Birder (RO1 DK54824 and RO1 DK57284).
The authors have declared associations with the following companies/organizations: Abbott Laboratories, Allergan, Astellas Pharma, Boehringer Ingleheim, Dynogen Pharmaceuticals, Eli Lilly, Hydra Biosciences, Johnson & Johnson, Lilly ICOS LLC, Novartis AG, Omeros, Pfizer, Roche Palo Alto LLC, and Sanofi Aventis. See the article online for full details of the relationship.
Lori A Birder, Department of Medicine, Renal-Electrolyte Division, and also holds a secondary appointment in the Department of Pharmacology, University of Pittsburgh School of Medicine, Pittsburgh, PA, USA.
William C de Groat, Department of Pharmacology, University of Pittsburgh School of Medicine, Pittsburgh, PA, USA.