Pharmacological effects of recombinant human tissue kallikrein on bradykinin B2 receptors. Issue 2 (10th February 2015) - Charest‐Morin, Xavier
Abstract: Tissue kallikrein (KLK‐1), a serine protease, initiates the release of bradykinin (BK)‐related peptides from low‐molecular weight kininogen. KLK‐1 and the BK B2 receptor (B2 R) mediate beneficial effects on the progression of type 2 diabetes and renal disease, but the precise role of KLK‐1 independent of its kinin‐forming activity remains unclear. We used DM199, a recombinant form of human KLK‐1, along with the isolated human umbilical vein, a robust bioassay of the B2 R, to address the previous claims that KLK‐1 directly binds to and activates the human B2 R, with possible receptor cleavage. DM199 (1–10 nmol/L) contracted the isolated vein via the B2 R, but in a tachyphylactic, kinin‐dependent manner, without desensitization of the tissue to exogenously added BK. In binding experiments with recombinant N‐terminally tagged myc‐B2 Rs expressed in HEK 293a cells, DM199 displaced [ 3 H]BK binding from the rabbit myc‐B2 R, but not from the human or rat myc‐B2 Rs. No evidence of myc‐B2 R degradation by immunoblot analysis was apparent following treatment of these 3 myc‐B2 R constructs with DM199 (30 min, ≤10 nmol/L). In HEK 293 cells stably expressing rabbit B2 R‐GFP, DM199 (11–108 pmol/L) elicited signaling‐dependent endocytosis and reexpression, while a higher concentration (1.1 nmol/L) induced a partially irreversible endocytosis of the construct (microscopy), paralleled by the appearance of free GFP in cells (immunoblotting, indicative of incomplete receptor down‐regulation). The pharmacology of DM199 at relevant concentrations (<10 nmol/L) is essentially based on the activity of locally generated kinins. Binding to and mild down‐regulation of the B2 R is possibly a species‐dependent idiosyncratic response to DM199. Abstract : e00119