Abstract
We report the cloning and sequencing from human reticulocytes of cDNA coding for the Cl- channel-associated protein, pICln. Human reticulocyte pICln (HRpICln) cDNA encodes a protein (predicted molecular mass 26293Da) identical with human non-pigmented ciliary epithelial cell pICln. By using full-length HRpICln cDNA (approx. 1.2 kb) to probe human lymphocyte metaphase-chromosome spreads, the location of the human ICln gene was mapped to 11q13 by fluorescence in situ hybridization analysis. Polyclonal antibodies to recombinant HRpICln detected bands at approx. 43 kDa and approx. 37 kDa in both normal (AA) and sickle (SS) red blood cell (RBC) ghost membranes. In SS ghosts, and in ghosts from a patient with autoimmune haemolytic anaemia with 9.8% reticulocytes, the amount of HRpICln was increased compared with AA ghosts, suggesting that the expression or membrane assembly of HRpICln is cell age-dependent. Laser scanning confocal fluorescent microscopy immunolocalized HRpICln largely to the RBC membrane. The increased staining intensity of HRpICln in a reticulocyte-enriched AA RBC density-separated fraction is consistent with a dependence of HRpICln membrane content on cell age. HRpICln and beta-actin form stable complexes in vivo, demonstrated with the yeast two-hybrid system. Low-ionic-strength extraction of ghost membranes, which results in the extraction of the spectrin-actin cytoskeleton, also results in the extraction of HRpICln, consistent with the possibility for the association of these proteins in RBCs in vivo. The results presented here establish the presence of the Cl- channel-associated protein, pICln, in human RBCs, and raises the possibility that this protein has a role in RBC Cl- transport and volume regulation in young RBCs. Moreover the association of RBC pICln with actin offers a model in which to test interactions between RBC ion channels and the cytoskeleton.
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- Ackerman M. J., Wickman K. D., Clapham D. E. Hypotonicity activates a native chloride current in Xenopus oocytes. J Gen Physiol. 1994 Feb;103(2):153–179. doi: 10.1085/jgp.103.2.153. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Anguita J., Chalfant M. L., Civan M. M., Coca-Prados M. Molecular cloning of the human volume-sensitive chloride conductance regulatory protein, pICln, from ocular ciliary epithelium. Biochem Biophys Res Commun. 1995 Mar 8;208(1):89–95. doi: 10.1006/bbrc.1995.1309. [DOI] [PubMed] [Google Scholar]
- Brugnara C., Bunn H. F., Tosteson D. C. Regulation of erythrocyte cation and water content in sickle cell anemia. Science. 1986 Apr 18;232(4748):388–390. doi: 10.1126/science.3961486. [DOI] [PubMed] [Google Scholar]
- Brugnara C. Membrane transport of Na and K and cell dehydration in sickle erythrocytes. Experientia. 1993 Feb 15;49(2):100–109. doi: 10.1007/BF01989413. [DOI] [PubMed] [Google Scholar]
- Brugnara C., Tosteson D. C. Cell volume, K transport, and cell density in human erythrocytes. Am J Physiol. 1987 Mar;252(3 Pt 1):C269–C276. doi: 10.1152/ajpcell.1987.252.3.C269. [DOI] [PubMed] [Google Scholar]
- Buyse G., de Greef C., Raeymaekers L., Droogmans G., Nilius B., Eggermont J. The ubiquitously expressed pICln protein forms homomeric complexes in vitro. Biochem Biophys Res Commun. 1996 Jan 26;218(3):822–827. doi: 10.1006/bbrc.1996.0146. [DOI] [PubMed] [Google Scholar]
- Canessa M., Fabry M. E., Blumenfeld N., Nagel R. L. Volume-stimulated, Cl(-)-dependent K+ efflux is highly expressed in young human red cells containing normal hemoglobin or HbS. J Membr Biol. 1987;97(2):97–105. doi: 10.1007/BF01869416. [DOI] [PubMed] [Google Scholar]
- Canessa M., Spalvins A., Nagel R. L. Volume-dependent and NEM-stimulated K+,Cl- transport is elevated in oxygenated SS, SC and CC human red cells. FEBS Lett. 1986 May 5;200(1):197–202. doi: 10.1016/0014-5793(86)80538-5. [DOI] [PubMed] [Google Scholar]
- DODGE J. T., MITCHELL C., HANAHAN D. J. The preparation and chemical characteristics of hemoglobin-free ghosts of human erythrocytes. Arch Biochem Biophys. 1963 Jan;100:119–130. doi: 10.1016/0003-9861(63)90042-0. [DOI] [PubMed] [Google Scholar]
- Fabry M. E., Nagel R. L. Heterogeneity of red cells in the sickler: a characteristic with practical clinical and pathophysiological implications. Blood Cells. 1982;8(1):9–15. [PubMed] [Google Scholar]
- Fairbanks G., Steck T. L., Wallach D. F. Electrophoretic analysis of the major polypeptides of the human erythrocyte membrane. Biochemistry. 1971 Jun 22;10(13):2606–2617. doi: 10.1021/bi00789a030. [DOI] [PubMed] [Google Scholar]
- Garay R. P., Nazaret C., Hannaert P. A., Cragoe E. J., Jr Demonstration of a [K+,Cl-]-cotransport system in human red cells by its sensitivity to [(dihydroindenyl)oxy]alkanoic acids: regulation of cell swelling and distinction from the bumetanide-sensitive [Na+,K+,Cl-]-cotransport system. Mol Pharmacol. 1988 Jun;33(6):696–701. [PubMed] [Google Scholar]
- Gschwentner M., Nagl U. O., Wöll E., Schmarda A., Ritter M., Paulmichl M. Antisense oligonucleotides suppress cell-volume-induced activation of chloride channels. Pflugers Arch. 1995 Aug;430(4):464–470. doi: 10.1007/BF00373882. [DOI] [PubMed] [Google Scholar]
- Guan K. L., Dixon J. E. Eukaryotic proteins expressed in Escherichia coli: an improved thrombin cleavage and purification procedure of fusion proteins with glutathione S-transferase. Anal Biochem. 1991 Feb 1;192(2):262–267. doi: 10.1016/0003-2697(91)90534-z. [DOI] [PubMed] [Google Scholar]
- Hall A. C., Ellory J. C. Evidence for the presence of volume-sensitive KCl transport in 'young' human red cells. Biochim Biophys Acta. 1986 Jun 26;858(2):317–320. doi: 10.1016/0005-2736(86)90338-x. [DOI] [PubMed] [Google Scholar]
- Hirsch R. E. Front-face fluorescence spectroscopy of hemoglobins. Methods Enzymol. 1994;232:231–246. doi: 10.1016/0076-6879(94)32050-0. [DOI] [PubMed] [Google Scholar]
- Hoffmann E. K., Dunham P. B. Membrane mechanisms and intracellular signalling in cell volume regulation. Int Rev Cytol. 1995;161:173–262. doi: 10.1016/s0074-7696(08)62498-5. [DOI] [PubMed] [Google Scholar]
- Joiner C. H. Cation transport and volume regulation in sickle red blood cells. Am J Physiol. 1993 Feb;264(2 Pt 1):C251–C270. doi: 10.1152/ajpcell.1993.264.2.C251. [DOI] [PubMed] [Google Scholar]
- Krapivinsky G. B., Ackerman M. J., Gordon E. A., Krapivinsky L. D., Clapham D. E. Molecular characterization of a swelling-induced chloride conductance regulatory protein, pICln. Cell. 1994 Feb 11;76(3):439–448. doi: 10.1016/0092-8674(94)90109-0. [DOI] [PubMed] [Google Scholar]
- Laemmli U. K. Cleavage of structural proteins during the assembly of the head of bacteriophage T4. Nature. 1970 Aug 15;227(5259):680–685. doi: 10.1038/227680a0. [DOI] [PubMed] [Google Scholar]
- Lauf P. K., Bauer J., Adragna N. C., Fujise H., Zade-Oppen A. M., Ryu K. H., Delpire E. Erythrocyte K-Cl cotransport: properties and regulation. Am J Physiol. 1992 Nov;263(5 Pt 1):C917–C932. doi: 10.1152/ajpcell.1992.263.5.C917. [DOI] [PubMed] [Google Scholar]
- Low P. S. Structure and function of the cytoplasmic domain of band 3: center of erythrocyte membrane-peripheral protein interactions. Biochim Biophys Acta. 1986 Sep 22;864(2):145–167. doi: 10.1016/0304-4157(86)90009-2. [DOI] [PubMed] [Google Scholar]
- McCurdy P. R., Sherman A. S. Irreversibly sickled cells and red cell survival in sickle cell anemia: a study with both DF32P and 51CR. Am J Med. 1978 Feb;64(2):253–258. doi: 10.1016/0002-9343(78)90053-0. [DOI] [PubMed] [Google Scholar]
- Orlov S. N., Kolosova I. A., Cragoe E. J., Gurlo T. G., Mongin A. A., Aksentsev S. L., Konev S. V. Kinetics and peculiarities of thermal inactivation of volume-induced Na+/H+ exchange, Na+,K+,2Cl- cotransport and K+,Cl- cotransport in rat erythrocytes. Biochim Biophys Acta. 1993 Sep 19;1151(2):186–192. doi: 10.1016/0005-2736(93)90103-7. [DOI] [PubMed] [Google Scholar]
- Paulmichl M., Li Y., Wickman K., Ackerman M., Peralta E., Clapham D. New mammalian chloride channel identified by expression cloning. Nature. 1992 Mar 19;356(6366):238–241. doi: 10.1038/356238a0. [DOI] [PubMed] [Google Scholar]
- Rybicki A. C., Heath R., Wolf J. L., Lubin B., Schwartz R. S. Deficiency of protein 4.2 in erythrocytes from a patient with a Coombs negative hemolytic anemia. Evidence for a role of protein 4.2 in stabilizing ankyrin on the membrane. J Clin Invest. 1988 Mar;81(3):893–901. doi: 10.1172/JCI113400. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Serjeant G. R., Serjeant B. E., Milner P. F. The irreversibly sickled cell; a determinant of haemolysis in sickle cell anaemia. Br J Haematol. 1969 Dec;17(6):527–533. doi: 10.1111/j.1365-2141.1969.tb01403.x. [DOI] [PubMed] [Google Scholar]
- Shi G., Cannizzaro L. A. Mapping of 29 YAC clones and identification of 3 YACs spanning the translocation t(3;8)(p14.2;q24.1) breakpoint at 8q24.1 in hereditary renal cell carcinoma. Cytogenet Cell Genet. 1996;75(2-3):180–185. doi: 10.1159/000134473. [DOI] [PubMed] [Google Scholar]
- Strange K., Emma F., Jackson P. S. Cellular and molecular physiology of volume-sensitive anion channels. Am J Physiol. 1996 Mar;270(3 Pt 1):C711–C730. doi: 10.1152/ajpcell.1996.270.3.C711. [DOI] [PubMed] [Google Scholar]
- Tanner M. J. Molecular and cellular biology of the erythrocyte anion exchanger (AE1). Semin Hematol. 1993 Jan;30(1):34–57. [PubMed] [Google Scholar]
- Temple G. F., Chang J. C., Kan Y. W. Authentic beta-globin mRNA sequences in homozygous betaO-thalassemia. Proc Natl Acad Sci U S A. 1977 Jul;74(7):3047–3051. doi: 10.1073/pnas.74.7.3047. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Towbin H., Staehelin T., Gordon J. Electrophoretic transfer of proteins from polyacrylamide gels to nitrocellulose sheets: procedure and some applications. Proc Natl Acad Sci U S A. 1979 Sep;76(9):4350–4354. doi: 10.1073/pnas.76.9.4350. [DOI] [PMC free article] [PubMed] [Google Scholar]