Serine protease activity in M-1 cortical collecting duct cells

An apical serine protease, channel-activating protease 1 (CAP1), augments sodium transport in A6 cells. Prostasin, a novel serine protease originally purified from seminal fluid, has been proposed to be the mammalian ortholog of CAP1. We have recently found functional evidence for a similar protease activity in the M-1 cortical collecting duct cell line. The purposes of the present studies were to determine whether prostasin (or CAP1) is present in collecting duct cells by use of mouse M-1 cells, to sequence mouse prostasin, and to further characterize the identity of the serine protease activity and additional functional features in M-1 cells. Using, mouse expressed sequence tag sequences that are highly homologous to the published human prostasin sequence as templates, reverse transcription-polymerase chain reaction and RACE (rapid amplification of cDNA ends) were used to sequence mouse prostasin mRNA, which shows 99% identical to published mouse CAP1 sequence. A single 1800-bp transcript was found by Northern analysis, and this was not altered by aldosterone. Equivalent short-circuit current (1,,), which represents sodium transport in these cells, dropped to 59 +/- 3% of control value within I hour of incubation with aprotinin, a serine protease inhibitor. Trypsin increased the I, in aprotinin-treated cells to the value of the control group within 5 minutes. Application of aprotinin not only inhibited amiloride sensitive I-eq but also reduced transepithelial resistance (R-te) to 43 +/- 2%, an effect not expected with simple inhibition of sodium channels. Trypsin partially reversed the effect of aprotinin on R-te. Another serine protease inhibitor, soybean trypsin inhibitor (STI), decreased I-eq in M-1 cells. STI inhibited I, gradually over 6 hours, and the inhibition of I, by 2 inhibitors was additive. STI decreased transepithelial resistance much less than did aprotinin. Neither aldosterone nor dexamethasone significantly augmented protease activity or prostasin mRNA levels, and in fact, dexamethasone decreased prostasin mRNA expression. In conclusion, although prostasin is present in M-1 cells and probably augments sodium transport in these cells, serine proteases probably have other effects (eg, resistance) in the collecting duct in addition to effects on sodium channels. Steroids do not alter these effects in M-I cells. Additional proteases are likely also present in mouse collecting duct cells.