Since its discovery in 1975, we now have a wealth of knowledge relating to
the biochemical, pharmacological and physiological actions of thromboxane A
(2) (TXA(2)) and its related metabolites. These molecular insights have bee
n greatly expedited by the molecular cloning and characterization of a cDNA
for the human TXA(2) receptor, now termed the T Prostanoid or TP receptor,
from a megakaryocytic/placental cDNA library in 1991, and later through th
e discovery of a cDNA encoding a second isoform of the human TP receptor in
1994. The requirement for two TP receptors in primates, but not in other s
pecies thus far investigated, is unclear, but points to potential species-s
pecific physiological differences. In this review, I will describe some rec
ent advances in the research field of TXA(2)/TP receptor signalling, focusi
ng particularly on studies pertaining to the human TP receptor isoforms.