SR2-CELLS( CAN PASS THROUGH CA2+ ENTRY PATHWAY ACTIVATED BY CA2+ DEPLETION, BUT CAN BE HARDLY TAKEN UP BY THE CA2+ STORES IN THE RAT SALIVARY ACINAR)

When Sr2+ was introduced to the external solution after the depletion of Ca2+ from stores of submandibular acinar cells by ACh stimulation, Sr2+ entered cytoplasm of the cell, like the case of Ca2+. SK&F 96365, a Ca2+ channel blocker, or Ni2+ blocked this divalent cation entry. S r2+ entering the cell continued to increase to a steady level, after t he cessation of stimulation, when Sr2+ present in the external solutio n, unlike the case of Ca2+. Ca2+ entered cells which had been stimulat ed with ACh in Sr2+-containing external solution. In the cells to whic h Sr2+ has been applied after the store depletion with ACh, Sr2+ canno t be released by the renewed ACh stimulation, unlike the case of Ca2+. Sr-89(2+) uptake by the parotidic microsomal fraction 100 min after a ddition of ATP was 15.08+/-0.70 nmol/mg protein, whereas Ca-45(2+) upt ake was 144.19+/-16.93 nmol/mg protein. It was concluded that in the s alivary acinar cells Sr2+ can be a substituent for Ca2+ in the mechani sm of entry from the extracellular fluid but cannot be in the mechanis m of uptake into the stores.