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Glaucoma/Lens

The Extracellular C-loop Domain Plays an Important Role in the Cell Adhesion Function of Aquaporin 0

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Pages 617-624 | Received 13 Jun 2016, Accepted 19 Jul 2016, Published online: 18 Oct 2016
 

ABSTRACT

Purpose: Although aquaporin 0 (AQP0) is a member of the AQP family, it has limited water permeability compared with other members. AQP0 may also have cell adhesion-related functions, but the evidence is still limited. Here, we studied the relationship of AQP0 to cell adhesion and determined the region required for cell adhesion.Methods: L-cell fibroblasts stably expressing AQP0 or AQP1 (L-AQP0 or L-AQP1) were established. One group of cells was stained with CellTracker Red and cultured into a confluent monolayer, whereas the other group was loaded with CellTracker Blue and seeded over the monolayer. To study cell adhesion, the percentages of lower and upper layer cells were measured using flow cytometry. To determine the region of AQP0 required for adhesion, activity was done by pull-down assay using glutathione S-transferase fusion proteins. To study the water permeability, Xenopus laevis oocyte expressing AQP0 wild-type or AQP0 mutated in C-loop was transferred to a hypotonic solution and photographed, and the diameter was measured to calculate the volume.Results: More cells adhered to the lower cells in the L-AQP0 homotypic pair than other pairs such as L-AQP1 homotypic or L-AQP0/L-AQP1 heterotypic pairs. Pull-down assays revealed that AQP0 could bind to itself via the C-loop extracellular domain. Furthermore, we determined that 109Pro and 110Pro in the C-loop were important for cell adhesion. However, mutation of the C-loop in AQP0 did not affect its water permeability.Conclusions: AQP0 is known to bind lipids in the opposing membrane. Our data suggest that this cell-to-cell adhesion occurs not only in the AQP0/liquids but also via AQP0/AQP0 interaction through the C-loop domain. Mutations in the C-loop amino acids did not affect the water permeability of AQP0 but did affect its cell adhesion function. These independent dual functions of AQP0 are important for lens transparency.

Declaration of Interest

The authors report no conflicts of interest. The authors alone are responsible for the content and writing of the paper.

Funding

This work was supported by a Japan Society for the Promotion of Science KAKENHI grants (numbers 26860149 and 16K18957) to Yosuke Nakazawa.

References

  • Agre P, Kozono D. Aquaporin water channels: molecular mechanisms for human diseases. FEBS Lett 2003;555:72–78.
  • Bassnett S, Wilmarth PA, David LL. The membrane proteome of the mouse lens fiber cell. Mol Vis 2009;15:2448–2463.
  • Piatigorsky J. Lens differentiation in vertebrates. A review of cellular and molecular features. Differentiation 1981;19:134–153.
  • Nielsen S, Smith BL, Christensen EI, Agre P. Distribution of the aquaporin CHIP in secretory and resorptive epithelia and capillary endothelia. Proc Natl Acad Sci USA 1993;90:7275–7279.
  • Hamann S, Zeuthen T, La Cour M, Nagelhus EA, Ottersen OP, Agre P, et al. Aquaporins in complex tissues: distribution of aquaporins 1–5 in human and rat eye. Am J Physiol 1998;274:C1332–C1345.
  • Wang Z, Han J, Schey KL. Spatial differences in an integral membrane proteome detected in laser capture microdissected samples. J Proteome Res 2008;7:2696–2702.
  • Ruiz-Ederra J, Verkman AS. Accelerated cataract formation and reduced lens epithelial water permeability in aquaporin-1-deficient mice. Invest Ophthalmol Vis Sci 2006;47:3960–3967.
  • Shiels A, Bassnett S. Mutations in the founder of the MIP gene family underlie cataract development in the mouse. Nat Genet 1996;12:212–215.
  • Berry V, Francis P, Kaushal S, Moore A, Bhattacharya S. Missense mutations in MIP underlie autosomal dominant ‘polymorphic’ and lamellar cataracts linked to 12q. Nat Genet 2000;25:15–17.
  • Sidjanin DJ, Parker-Wilson DM, Neuhäuser-Klaus A, Pretsch W, Favor J, Deen PM, et al. A 76-bp deletion in the Mip gene causes autosomal dominant cataract in Hfi mice. Genomics 2001;74:313–319.
  • Okamura T, Miyoshi I, Takahashi K, Mototani Y, Ishigaki S, Kon Y, et al. Bilateral congenital cataracts result from a gain-of-function mutation in the gene for aquaporin-0 in mice. Genomics 2003;81:361–368.
  • Geyer DD, Spence MA, Johannes M, Flodman P, Clancy KP, Berry R, et al. Novel single-base deletional mutation in major intrinsic protein (MIP) in autosomal dominant cataract. Am J Ophthalmol 2006;141:761–763.
  • Gu F, Zhai H, Li D, Zhao L, Li C, Huang S, et al. A novel mutation in major intrinsic protein of the lens gene (MIP) underlies autosomal dominant cataract in a Chinese family. Mol Vis 2007;13:1651–1656.
  • Zampighi GA, Kreman M, Boorer KJ, Loo DD, Bezanilla F, Chandy G, et al. A method for determining the unitary functional capacity of cloned channels and transporters expressed in Xenopus laevis oocytes. J Membr Biol 1995;148:65–78.
  • Oliva R, Calamita G, Thornton JM, Pellegrini-Calace M. Electrostatics of aquaporin and aquaglyceroporin channels correlates with their transport selectivity. Proc Natl Acad Sci USA 2010;107:4135–4140.
  • Zampighi G, Simon SA, Robertson JD, McIntosh TJ, Costello MJ. On the structural organization of isolated bovine lens fiber junctions. J Cell Biol 1982;93:175–189.
  • Gonen T, Cheng Y, Sliz P, Hiroaki Y, Fujiyoshi Y, Harrison SC, et al. Lipid-protein interactions in double-layered two-dimensional AQP0 crystals. Nature 2005;438:633–638.
  • Kumari SS, Varadaraj K. Intact AQP0 performs cell-to-cell adhesion. Biochem Biophys Res Commun 2009;390:1034–1039.
  • Wang W, Jiang J, Zhu Y, Li J, Jin C, Shentu X, et al. A novel mutation in the major intrinsic protein (MIP) associated with autosomal dominant congenital cataracts in a Chinese family. Mol Vis 2010;16:534–539.
  • Nakazawa Y, Oka M, Mitsuishi A, Bando M, Takehana M. Quantitative analysis of ascorbic acid permeability of aquaporin 0 in the lens. Biochem Biophys Res Commun 2011;415:125–130.
  • Varadaraj K, Kumari SS, Mathias RT. Transgenic expression of AQP1 in the fiber cells of AQP0 knockout mouse: effects on lens transparency. Exp Eye Res 2010;91:393–404.
  • Nakazawa Y, Oka M, Furuki K, Mitsuishi A, Nakashima E, Takehana M. The effect of the interaction between aquaporin 0 (AQP0) and the filensin tail region on AQP0 water permeability. Mol Vis 2011;17:3191–3199.
  • Ball LE, Little M, Nowak MW, Garland DL, Crouch RK, Schey KL. Water permeability of C-terminally truncated aquaporin 0 (AQP0 1-243) observed in the aging human lens. Invest Ophthalmol Vis Sci 2003;44:4820–4828.
  • Nagafuchi A, Shirayoshi Y, Okazaki K, Yasuda K, Takeichi M. Transformation of cell adhesion properties by exogenously introduced E-cadherin cDNA. Nature 1987;329:341–343.
  • Tait MJ, Saadoun S, Bell BA, Papadopoulos MC. Water movements in the brain: role of aquaporins. Trends Neurosci. 2008;31:37–43.
  • Gonen T, Sliz P, Kistler J, Cheng Y, Walz T. Aquaporin-0 membrane junctions reveal the structure of a closed water pore. Nature 2004;429:193–197.
  • Suzuki H, Nishikawa K, Hiroaki Y, Fujiyoshi Y. Formation of aquaporin-4 arrays is inhibited by palmitoylation of N-terminal cysteine residues. Biochim Biophys Acta 2008;1778:1181–1189.
  • Kumari SS, Gandhi J, Mustehsan MH, Eren S, Varadaraj K. Functional characterization of an AQP0 missense mutation, R33C, that causes dominant congenital lens cataract, reveals impaired cell-to-cell adhesion. Exp Eye Res 2013;116:371–385.
  • Schey KL, Little M, Fowler JG, Crouch RK. Characterization of human lens major intrinsic protein structure. Invest Ophthalmol Vis Sci 2000;41:175–182.
  • Girsch SJ, Peracchia C. Calmodulin interacts with a C-terminus peptide from the lens membrane protein MIP26. Curr Eye Res 1991;10:839–849.
  • Yu XS, Yin X, Lafer EM, Jiang JX. Developmental regulation of the direct interaction between the intracellular loop of connexin 45.6 and the C terminus of major intrinsic protein (aquaporin-0). J Biol Chem 2005;280:22081–22090.
  • Fan J, Donovan AK, Ledee DR, Zelenka PS, Fariss RN, Chepelinsky AB. gammaE-crystallin recruitment to the plasma membrane by specific interaction between lens MIP/aquaporin-0 and gammaE-crystallin. Invest Ophthalmol Vis Sci 2004;45:863–871.
  • Lindsey-Rose KM, Gourdie RG, Prescott AR, Quinlan RA, Crouch RK, Schey KL. The C terminus of lens aquaporin 0 interacts with the cytoskeletal proteins filensin and CP49. Invest Ophthalmol Vis Sci 2006;47:1562–1570.
  • Oka M, Kudo H, Sugama N, Asami Y, Takehana M. The function of filensin and phakinin in lens transparency. Mol Vis 2008;14:815–822.

Additional information

Funding

This work was supported by a Japan Society for the Promotion of Science KAKENHI grants (numbers 26860149 and 16K18957) to Yosuke Nakazawa.

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