Human kidney cortex and medulla contain ETA and ETB receptors in a 30:70 ratio, which can be identified using selective ligands like sarafotoxin-6c and BQ123.
High affinity and high density endothelin (ET)-binding sites were identified in membranes prepared from human kidney cortex and medulla. Saturation binding experiments performed in membranes prepared from cortex and medulla using 125IET-1 and 125IET-3 revealed that the proportion of 125IET-3-binding sites was 30-35% less than that of 125IET-1-binding sites. The apparent dissociation constants and maximum binding for 125IET-1 and 125IET-3 to membranes from cortex were 91 +/- 5 pM and 165 +/- 10 fmol/mg protein, and 117 +/- 9 pM and 110 +/- 7 fmol/mg protein, respectively, whereas in medulla they were 139 +/- 10 pM and 360 +/- 11 fmol/mg protein, and 142 +/- 11 pM and 245 +/- 15 fmol/mg protein, respectively. In the presence of 10 nM sarafotoxin-6c, which is selective for ETB receptors, 125IET-1 binding was decreased by 65-70%, whereas 125IET-3 binding was totally abolished, suggesting that 65-70% of 125IET-1 binding and 100% of 125IET-3 binding was to ETB receptors. This was further confirmed by the use of a cyclic pentapeptide cyclo(D-Trp,D-Asp,L-Pro, D-Val,L-Leu) (BQ123), which is selective for ETA receptors. In the presence of 1 microM BQ123, 125IET-1 binding was decreased by 25-30%, whereas 125IET-3 binding was unaffected, confirming that 30-35% of ET receptors belong to the ETA subtypes, and that 125IET-1 bound to both ETA and ETB receptors with the same high affinity, but 125IET-3 bound only to ETB receptors with high affinity. These results suggest that human kidney cortex and medulla contain ETA and ETB receptors in a ratio of 30:70, and that sarafotoxin-6c and BQ123 are valuable tools in identifying the subtype of ET receptors in various tissues.
Nambi et al. (1992) studied this question.