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XB-ART-42553
Am J Physiol Cell Physiol. May 1, 2011; 300 (5): C1034-46.

Functional characterization and modified rescue of novel AE1 mutation R730C associated with overhydrated cation leak stomatocytosis.

Stewart AK , Kedar PS , Shmukler BE , Vandorpe DH , Hsu A , Glader B , Rivera A , Brugnara C , Alper SL .


Abstract
We report the novel, heterozygous AE1 mutation R730C associated with dominant, overhydrated, cation leak stomatocytosis and well-compensated anemia. Parallel elevations of red blood cell cation leak and ouabain-sensitive Na(+) efflux (pump activity) were apparently unaccompanied by increased erythroid cation channel-like activity, and defined ouabain-insensitive Na(+) efflux pathways of nystatin-treated cells were reduced. Epitope-tagged AE1 R730C at the Xenopus laevis oocyte surface exhibited severely reduced Cl(-) transport insensitive to rescue by glycophorin A (GPA) coexpression or by methanethiosulfonate (MTS) treatment. AE1 mutant R730K preserved Cl(-) transport activity, but R730 substitution with I, E, or H inactivated Cl(-) transport. AE1 R730C expression substantially increased endogenous oocyte Na(+)-K(+)-ATPase-mediated (86)Rb(+) influx, but ouabain-insensitive flux was minimally increased and GPA-insensitive. The reduced AE1 R730C-mediated sulfate influx did not exhibit the wild-type pattern of stimulation by acidic extracellular pH (pH(o)) and, unexpectedly, was partially rescued by exposure to sodium 2-sulfonatoethyl methanethiosulfonate (MTSES) but not to 2-aminoethyl methanethiosulfonate hydrobromide (MTSEA) or 2-(trimethylammonium)ethyl methanethiosulfonate bromide (MTSET). AE1 R730E correspondingly exhibited acid pH(o)-stimulated sulfate uptake at rates exceeding those of wild-type AE1 and AE1 R730K, whereas mutants R730I and R730H were inactive and pH(o) insensitive. MTSES-treated oocytes expressing AE1 R730C and untreated oocytes expressing AE1 R730E also exhibited unprecedented stimulation of Cl(-) influx by acid pH(o). Thus recombinant cation-leak stomatocytosis mutant AE1 R730C exhibits severely reduced anion transport unaccompanied by increased Rb(+) and Li(+) influxes. Selective rescue of acid pH(o)-stimulated sulfate uptake and conferral of acid pH(o)-stimulated Cl(-) influx, by AE1 R730E and MTSES-treated R730C, define residue R730 as critical to selectivity and regulation of anion transport by AE1.

PubMed ID: 21209359
PMC ID: PMC3093938
Article link: Am J Physiol Cell Physiol.
Grant support: DK-34854 NIDDK NIH HHS , DK-43495 NIDDK NIH HHS , HL-077765 NHLBI NIH HHS , HL-077765 NHLBI NIH HHS , HL-077765 NHLBI NIH HHS , HL-077765 NHLBI NIH HHS , HL-077765 NHLBI NIH HHS , HL-077765 NHLBI NIH HHS , HL-090632 NHLBI NIH HHS , HL-090632 NHLBI NIH HHS , HL-090632 NHLBI NIH HHS , HL-090632 NHLBI NIH HHS , HL-090632 NHLBI NIH HHS , HL-090632 NHLBI NIH HHS

Genes referenced: slc4a1
Antibodies referenced:
Morpholinos referenced:

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