2 research outputs found
Insulin receptor-related receptor as an extracellular alkali sensor
17sireservedThe insulin receptor-related receptor (IRR), an orphan receptor tyrosine kinase of the insulin receptor family, can be activated by alkaline media both in vitro and in vivo at pH >7.9. The alkali-sensing property of IRR is conserved in frog, mouse, and human. IRR activation is specific, dose-dependent and quickly reversible and demonstrates positive cooperativity. It also triggers receptor conformational changes and elicits intracellular signaling. The pH sensitivity of IRR is primarily defined by its L1F extracellular domains. IRR is predominantly expressed in organs that come in contact with mildly alkaline media. In particular, IRR is expressed in the cell subsets of the kidney that secrete bicarbonate into urine. Disruption of IRR in mice impairs the renal response to alkali loading attested by development of metabolic alkalosis and decreased urinary bicarbonate excretion in response to this challenge. We therefore postulate that IRR is an alkali sensor that functions in the kidney to manage metabolic bicarbonate excess.mixedDeyev, Igor E; Sohet, Fabien; Vassilenko, Konstantin P; Serova, Oxana V; Popova, Nadezhda V; Zozulya, Sergey A; Burova, Elena B; Houillier, Pascal; Rzhevsky, Dmitry I; Berchatova, Anastasija A; Murashev, Arkady N; Chugunov, Anton O; Efremov, Roman G; Nikol'Sky, Nikolai N; Bertelli, Eugenio; Eladari, Dominique; Petrenko, Alexander G.Deyev, Igor E; Sohet, Fabien; Vassilenko, Konstantin P; Serova, Oxana V; Popova, Nadezhda V; Zozulya, Sergey A; Burova, Elena B; Houillier, Pascal; Rzhevsky, Dmitry I; Berchatova, Anastasija A; Murashev, Arkady N; Chugunov, Anton O; Efremov, Roman G; Nikol'Sky, Nikolai N; Bertelli, Eugenio; Eladari, Dominique; Petrenko, Alexander G
Structural Determinants of the Insulin Receptor-related Receptor Activation by Alkali
IRR is a member of the insulin receptor (IR) family that does not have any known agonist of a peptide nature but can be activated by mildly alkaline medium and was thus proposed to function as an extracellular pH sensor. IRR activation by alkali is defined by its N-terminal extracellular region. To reveal key structural elements involved in alkali sensing, we developed an in vitro method to quantify activity of IRR and its mutants. Replacing the IRR L1C domains (residues 1–333) or L2 domain (residues 334–462) or both with the homologous fragments of IR reduced the receptor activity to 35, 64, and 7% percent, respectively. Within L1C domains, five amino acid residues (Leu-135, Gly-188, Arg-244, and vicinal His-318 and Lys-319) were identified as IRR-specific by species conservation analysis of the IR family. These residues are exposed and located in junctions between secondary structure folds. The quintuple mutation of these residues to alanine had the same negative effect as the entire L1C domain replacement, whereas none of the single mutations was as effective. Separate mutations of these five residues and of L2 produced partial negative effects that were additive. The pH dependence of cell-expressed mutants (L1C and L2 swap, L2 plus triple LGR mutation, and L2 plus quintuple LGRHK mutation) was shifted toward alkalinity and, in contrast with IRR, did not show significant positive cooperativity. Our data suggest that IRR activation is not based on a single residue deprotonation in the IRR ectodomain but rather involves synergistic conformational changes at multiple points