We have investigated endoproteolytic processing of protachykinin B and
regulated release of neurokinin B following transfection into heterol
ogous endocrine cell lines, AtT-20 and MING. Both of the transfected c
ell lines produced mature neurokinin B and secreted it in response to
a secretagogue, 8-Br-cAMP. Northern blot analysis of PC3 and PC2, two
recently cloned Kex2-like processing endoprotease, showed that AtT-20
cells expressed PC3 mRNA, while MING cells expressed both PC2 and PC3
mRNAs. These data suggest that protachykinin B is processed to neuroki
nin B by at least PC3 within the regulated secretory pathway.