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Active ion transport and coupled osmotic water flow are essential to maintain ocular surface health. We investigated regional differences in the ion transport activities of the rat conjunctivas and compared these activities with those of cornea and lacrimal gland. The epithelial sodium channel (ENaC), sodium/glucose cotransporter 1 (Slc5a1), transmembrane protein 16 (Tmem16a, b, f, and g), cystic fibrosis transmembrane conductance regulator (Cftr), and mucin (Muc4, 5ac, and 5b) mRNA expression was characterized by RT-PCR. ENaC proteins were measured by Western blot. Prespecified regions (palpebral, fornical, and bulbar) of freshly isolated conjunctival tissues and cell cultures were studied electrophysiologically with Ussing chambers. The transepithelial electrical potential difference (PD) of the ocular surface was also measured in vivo. The effect of amiloride and UTP on the tear volume was evaluated in lacrimal gland excised rats. All selected genes were detected but with different expression patterns. We detected αENaC protein in all tissues, βENaC in palpebral and fornical conjunctiva, and γENaC in all tissues except lacrimal glands. Electrophysiological studies of conjunctival tissues and cell cultures identified functional ENaC, SLC5A1, CFTR, and TMEM16. Fornical conjunctiva exhibited the most active ion transport under basal conditions amongst conjunctival regions. PD measurements confirmed functional ENaC-mediated Na(+) transport on the ocular surface. Amiloride and UTP increased tear volume in lacrimal gland excised rats. This study demonstrated that the different regions of the conjunctiva exhibited a spectrum of ion transport activities. Understanding the specific functions of distinct regions of the conjunctiva may foster a better understanding of the physiology maintaining hydration of the ocular surface.
Almaça,
TMEM16 proteins produce volume-regulated chloride currents that are reduced in mice lacking TMEM16A.
2009, Pubmed
Almaça,
TMEM16 proteins produce volume-regulated chloride currents that are reduced in mice lacking TMEM16A.
2009,
Pubmed
Al-Nakkash,
Activation of a CFTR-mediated chloride current in a rabbit corneal epithelial cell line.
2001,
Pubmed
Alvarez,
Phorbol ester modulation of active ion transport across the rabbit conjunctival epithelium.
1999,
Pubmed
Alvarez,
Serotonin-elicited inhibition of Cl(-) secretion in the rabbit conjunctival epithelium.
2001,
Pubmed
Alvarez,
Cl- secretory effects of EBIO in the rabbit conjunctival epithelium.
2005,
Pubmed
Bron,
Functional aspects of the tear film lipid layer.
2004,
Pubmed
Caputo,
TMEM16A, a membrane protein associated with calcium-dependent chloride channel activity.
2008,
Pubmed
Chandler,
Immunologic defense mechanisms of the ocular surface.
1983,
Pubmed
Dartt,
Regulation of mucin and fluid secretion by conjunctival epithelial cells.
2002,
Pubmed
Dartt,
Neural regulation of lacrimal gland secretory processes: relevance in dry eye diseases.
2009,
Pubmed
Ding,
Duct system of the rabbit lacrimal gland: structural characteristics and role in lacrimal secretion.
2010,
Pubmed
Donaldson,
Sodium channels and cystic fibrosis.
2007,
Pubmed
García-Caballero,
ENaC proteolytic regulation by channel-activating protease 2.
2008,
Pubmed
Gentzsch,
The cystic fibrosis transmembrane conductance regulator impedes proteolytic stimulation of the epithelial Na+ channel.
2010,
Pubmed
Ghanem,
The role of epithelial P2Y2 and P2Y4 receptors in the regulation of intestinal chloride secretion.
2005,
Pubmed
Gipson,
Cellular origin of mucins of the ocular surface tear film.
1998,
Pubmed
Gipson,
The ocular surface: the challenge to enable and protect vision: the Friedenwald lecture.
2007,
Pubmed
Grubb,
Hyperabsorption of Na+ and raised Ca(2+)-mediated Cl- secretion in nasal epithelia of CF mice.
1994,
Pubmed
Hara,
The effect of topical amiloride eye drops on tear quantity in rabbits.
2010,
Pubmed
Hosoya,
Contribution of Na(+)-glucose cotransport to the short-circuit current in the pigmented rabbit conjunctiva.
1996,
Pubmed
Hosoya,
Nucleotide stimulation of Cl(-) secretion in the pigmented rabbit conjunctiva.
1999,
Pubmed
Johnson,
Changes in the tear film and ocular surface from dry eye syndrome.
2004,
Pubmed
Jumblatt,
Regulation of ocular mucin secretion by P2Y2 nucleotide receptors in rabbit and human conjunctiva.
1998,
Pubmed
Kompella,
Active chloride transport in the pigmented rabbit conjunctiva.
1993,
Pubmed
Kompella,
Possible existence of Na(+)-coupled amino acid transport in the pigmented rabbit conjunctiva.
1995,
Pubmed
Levin,
CFTR-regulated chloride transport at the ocular surface in living mice measured by potential differences.
2005,
Pubmed
Levin,
Potential difference measurements of ocular surface Na+ absorption analyzed using an electrokinetic model.
2006,
Pubmed
Li,
Rabbit conjunctival epithelium transports fluid, and P2Y2(2) receptor agonists stimulate Cl(-) and fluid secretion.
2001,
Pubmed
Masilamani,
Aldosterone-mediated regulation of ENaC alpha, beta, and gamma subunit proteins in rat kidney.
1999,
Pubmed
McCulley,
The lipid layer: the outer surface of the ocular surface tear film.
2001,
Pubmed
McKown,
Lacritin and other new proteins of the lacrimal functional unit.
2009,
Pubmed
Montés-Micó,
The tear film and the optical quality of the eye.
2010,
Pubmed
Morkeberg,
Ocular findings in cystic fibrosis patients receiving vitamin A supplementation.
1995,
Pubmed
Mrugacz,
IL-8 and IFN-gamma in tear fluid of patients with cystic fibrosis.
2006,
Pubmed
Murakami,
P2Y(2) receptor stimulation increases tear fluid secretion in rabbits.
2000,
Pubmed
Nemet,
Transplantation of newborn lacrimal gland cells in a rat model of reduced tear secretion.
2007,
Pubmed
Oh,
Development of selective blockers for Ca²(+)-activated Cl channel using Xenopus laevis oocytes with an improved drug screening strategy.
2008,
Pubmed
,
Xenbase
Pintor,
Effects of diadenosine polyphosphates on tear secretion in New Zealand white rabbits.
2002,
Pubmed
Rock,
Transmembrane protein 16A (TMEM16A) is a Ca2+-regulated Cl- secretory channel in mouse airways.
2009,
Pubmed
Rolando,
The ocular surface and tear film and their dysfunction in dry eye disease.
2001,
Pubmed
Rossier,
Activation of the epithelial sodium channel (ENaC) by serine proteases.
2009,
Pubmed
Selvam,
Transepithelial bioelectrical properties of rabbit acinar cell monolayers on polyester membrane scaffolds.
2007,
Pubmed
Sheppard,
The ocular surface in cystic fibrosis.
1989,
Pubmed
Shiue,
Pharmacological modulation of fluid secretion in the pigmented rabbit conjunctiva.
2000,
Pubmed
Stephan,
ANO2 is the cilial calcium-activated chloride channel that may mediate olfactory amplification.
2009,
Pubmed
Stern,
The role of the lacrimal functional unit in the pathophysiology of dry eye.
2004,
Pubmed
Sun,
Expression, localization, and functional evaluation of CFTR in bovine corneal endothelial cells.
2002,
Pubmed
Turner,
Presence of CFTR in the conjunctival epithelium.
2002,
Pubmed
Ubels,
Gene expression in rat lacrimal gland duct cells collected using laser capture microdissection: evidence for K+ secretion by duct cells.
2006,
Pubmed
Walcott,
Fluid secretion and the Na+-K+-2Cl- cotransporter in mouse exorbital lacrimal gland.
2005,
Pubmed
Watsky,
Comparison of conjunctival and corneal surface areas in rabbit and human.
1988,
Pubmed
Yu,
MUC19 expression in human ocular surface and lacrimal gland and its alteration in Sjögren syndrome patients.
2008,
Pubmed