A SARCO ENDOPLASMIC-RETICULUM CA2-ATPASE 3-TYPE CA2+ PUMP IS EXPRESSED IN PLATELETS, IN LYMPHOID-CELLS, AND IN MAST-CELLS()

An organellar-type of Ca2+ pump formerly detected by means of its phos phoprotein intermediate in platelets and in lymphoid cells, and which runs in acid gels at 97 kDa, is now characterized as sarco/endoplasmic reticulum Ca2+ ATPase 3 (SERCA3). SERCA3 is co-expressed in these cel ls along with the housekeeping SERCA2b. This conclusion is based on th e following observations. 1) Tryptic digestion the phosphoprotein inte rmediate of SERCA3 expressed in COS cells yields a phosphorylated frag ment of about 80 kDa, which can be clearly distinguished from the 57-k Da fragments formed in the SERCA1 and SERCA2 pumps. This 80-kDa fragme nt comigrates with a similar phosphoprotein fragment previously observ ed in human platelets (Papp, B., Enyedi, A., Paszty, K., Kovacs, T., S arkadi, B., Gardos, G., Wuytack, F., and Enouf, J. (1992) Biochem. J. 288, 297-302). 2) An antiserum directed against an NH2-terminal SERCA3 -specific peptide (N89) reacts with SERCA3 expressed in COS cells and with the 97-kDa protein in rat platelets and the corresponding protein in human platelets. Likewise an antiserum against the rat SERCA3 term inus (C90) binds to SERCA3 expressed in COS cells and to the 97-kDa ba nd in rat platelets, but it does not recognize the human platelet pump . In conformity with the predicted absence of the T1 tryptic cleavage site in SERCA3, the autophosphorylated aspartyl residue and the COOH-t erminal epitope were co-localized on the 80-kDa fragment. 3) The co-ex pression of nearly equal levels of SERCA3 and SERCA2b messengers in hu man lymphoblastoid Jurkat cells and in proliferating rat mucosal mast cells was also demonstrated by reverse transcriptase polymerase chain reaction.