PURPOSE: It has been established that Na,K-ATPase activity is higher in lens epithelium than fibers. However, others have suggested the Na,K-ATPase enzyme may be inactive or absent in the central 10% of the epithelium. Studies were conducted to measure and compare Na,K-ATPase specific activity and to examine Na,K-ATPase protein expression in the anterior and equatorial regions of porcine lens epithelium. METHODS: Na,K-ATPase activity was determined by measuring the ouabain-sensitive rate of adenosine triphosphate (ATP) hydrolysis. Western blot analysis was used to detect Na,K-ATPase catalytic subunit (alpha) and glycoprotein subunit (beta) protein as well as beta-actin which was used as a loading control. RESULTS: Na,K-ATPase specific activity was more than two times higher in the equatorial epithelium than the anterior 50% of the epithelium. However, the abundance of Na,K-ATPase alpha1 isoform protein was similar in the two regions. Neither the alpha2 nor alpha3 Na,K-ATPase isoform could be detected in the anterior or equatorial epithelium, but Na,K-ATPase beta1 protein was detected in both regions. In contrast to the observed regional difference in Na,K-ATPase activity, the activity of a different P-type ATPase, plasma membrane Ca-ATPase (PMCA), was not significantly different in the anterior and central epithelium. Western blot analysis indicated the presence of two PMCA isoforms, PMCA2, and PMCA4. CONCLUSIONS: Na,K-ATPase activity is significantly higher at the equatorial region of the epithelium compared with the anterior, even though the level of Na,K-ATPase protein is similar in the two regions. It is possible that nonuniform distribution of functional Na,K-ATPase activity contributes to the driving force for circulating solute movement through the lens fiber mass.
PURPOSE: It has been established that Na,K-ATPase activity is higher in lens epithelium than fibers. However, others have suggested the Na,K-ATPase enzyme may be inactive or absent in the central 10% of the epithelium. Studies were conducted to measure and compare Na,K-ATPase specific activity and to examine Na,K-ATPase protein expression in the anterior and equatorial regions of porcine lens epithelium. METHODS: Na,K-ATPase activity was determined by measuring the ouabain-sensitive rate of adenosine triphosphate (ATP) hydrolysis. Western blot analysis was used to detect Na,K-ATPase catalytic subunit (alpha) and glycoprotein subunit (beta) protein as well as beta-actin which was used as a loading control. RESULTS: Na,K-ATPase specific activity was more than two times higher in the equatorial epithelium than the anterior 50% of the epithelium. However, the abundance of Na,K-ATPase alpha1 isoform protein was similar in the two regions. Neither the alpha2 nor alpha3 Na,K-ATPase isoform could be detected in the anterior or equatorial epithelium, but Na,K-ATPase beta1 protein was detected in both regions. In contrast to the observed regional difference in Na,K-ATPase activity, the activity of a different P-type ATPase, plasma membrane Ca-ATPase (PMCA), was not significantly different in the anterior and central epithelium. Western blot analysis indicated the presence of two PMCA isoforms, PMCA2, and PMCA4. CONCLUSIONS: Na,K-ATPase activity is significantly higher at the equatorial region of the epithelium compared with the anterior, even though the level of Na,K-ATPase protein is similar in the two regions. It is possible that nonuniform distribution of functional Na,K-ATPase activity contributes to the driving force for circulating solute movement through the lens fiber mass.
Authors: Junyuan Gao; Huan Wang; Xiurong Sun; Kulandaiappan Varadaraj; Leping Li; Thomas W White; Richard T Mathias Journal: Invest Ophthalmol Vis Sci Date: 2013-11-01 Impact factor: 4.799
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Authors: Mohammad Shahidullah; Amritlal Mandal; Richard T Mathias; Junyuan Gao; David Križaj; Sarah Redmon; Nicholas A Delamere Journal: Am J Physiol Cell Physiol Date: 2020-04-15 Impact factor: 4.249
Authors: Junyuan Gao; Xiurong Sun; Francisco J Martinez-Wittinghan; Xiaohua Gong; Thomas W White; Richard T Mathias Journal: J Gen Physiol Date: 2004-10 Impact factor: 4.086