TY - JOUR
T1 - The distal convoluted tubule of rabbit kidney does not express a functional sodium channel
AU - Velázquez, Heino
AU - Silva, Teresa
AU - Andújar, Eleanor
AU - Desir, Gary V.
AU - Ellison, David H.
AU - Greger, Rainer
PY - 2001
Y1 - 2001
N2 - We sought to assess whether the distal convoluted tubule (DCT) segment of the rabbit nephron expresses a functional epithelial sodium channel. First, the transepithelial voltage (Vte, lumen vs. bath) was measured in isolated perfused DCT segments (assessed separately in the upstream half and the downstream half of the DCT). Vte was zero and not affected by amiloride or barium in the upstream DCT. Vte was sometimes negative in the downstream DCT and depolarized by amiloride and hyperpolarized by barium, suggesting inclusion of connecting tubule (CNT) cells. To determine expression of epithelial sodium channel (ENaC) mRNA subunits by the upstream DCT, rabbit α-, β-, and γ-ENaC cDNA fragments were cloned and primers were selected for single-nephron RT-PCR analysis. Although α-ENaC was expressed by the DCT, β- and γ-ENaC were not detected in the DCT. In contrast, the CNT, CCD, and outer medullary collecting duct (OMCD) expressed all three subunits. Nedd4 was also not detected in the DCT but was expressed by the CNT, CCD, and OMCD. When upstream DCT fragments were grown to confluent monolayers in primary culture, the epithelia exhibited negative voltages and high transepithelial resistances and expressed mRNA for all three ENaC subunits as well as for Nedd4. The absence of a negative voltage and failure to detect transcript for β- and γ-ENaC and Nedd4 in the native rabbit DCT suggest that the sodium channel is not a significant pathway for sodium absorption by this segment. The phenotype conversion observed when DCT cells are grown in culture does not rule out the possibility that there may be conditions in which the DCT in the intact kidney expresses sodium channel activity. The results are consistent with the notion that DCT sodium transport is predominantly, if not exclusively, electroneutral.
AB - We sought to assess whether the distal convoluted tubule (DCT) segment of the rabbit nephron expresses a functional epithelial sodium channel. First, the transepithelial voltage (Vte, lumen vs. bath) was measured in isolated perfused DCT segments (assessed separately in the upstream half and the downstream half of the DCT). Vte was zero and not affected by amiloride or barium in the upstream DCT. Vte was sometimes negative in the downstream DCT and depolarized by amiloride and hyperpolarized by barium, suggesting inclusion of connecting tubule (CNT) cells. To determine expression of epithelial sodium channel (ENaC) mRNA subunits by the upstream DCT, rabbit α-, β-, and γ-ENaC cDNA fragments were cloned and primers were selected for single-nephron RT-PCR analysis. Although α-ENaC was expressed by the DCT, β- and γ-ENaC were not detected in the DCT. In contrast, the CNT, CCD, and outer medullary collecting duct (OMCD) expressed all three subunits. Nedd4 was also not detected in the DCT but was expressed by the CNT, CCD, and OMCD. When upstream DCT fragments were grown to confluent monolayers in primary culture, the epithelia exhibited negative voltages and high transepithelial resistances and expressed mRNA for all three ENaC subunits as well as for Nedd4. The absence of a negative voltage and failure to detect transcript for β- and γ-ENaC and Nedd4 in the native rabbit DCT suggest that the sodium channel is not a significant pathway for sodium absorption by this segment. The phenotype conversion observed when DCT cells are grown in culture does not rule out the possibility that there may be conditions in which the DCT in the intact kidney expresses sodium channel activity. The results are consistent with the notion that DCT sodium transport is predominantly, if not exclusively, electroneutral.
KW - Amiloride
KW - Cell culture
KW - Cloning
KW - Epithelial sodium channel
KW - Nedd4
UR - http://www.scopus.com/inward/record.url?scp=0034984531&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=0034984531&partnerID=8YFLogxK
U2 - 10.1152/ajprenal.2001.280.3.f530
DO - 10.1152/ajprenal.2001.280.3.f530
M3 - Article
C2 - 11181416
AN - SCOPUS:0034984531
SN - 0363-6127
VL - 280
SP - F530-F539
JO - American journal of physiology. Renal physiology
JF - American journal of physiology. Renal physiology
IS - 3 49-3
ER -