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J. Biol. Chem., Vol. 265, Issue 9, 4775-4777, Mar, 1990
LW Jiang, VM Maher, JJ McCormick and M Schindler
The pH of the intralysosomal compartment of fibroblasts in culture was
monitored by measuring the fluorescence emission intensity at 530 nm of
fluid phase pinocytosed fluorescein-conjugated dextrans (FITC-dextrans)
excited at 488 and 457 nm. Following the procedure of Ohkuma and Poole
(Ohkuma, S., and Poole, B. (1978) Proc. Natl. Acad. Sci. U. S. A. (1978)
75, 3327-3331), a relationship was established between the fluorescence
emission intensity of the FITC-dextrans and pH. This correlation was used
to determine the intralysosomal apparent pH (pHapp) of a series of
fibroblast cultures. The mean intralysosomal pHapp values of nontransformed
mouse 3T3 fibroblasts and an infinite life-span human fibroblast cell
strain, designated MSU-1.1, was 5.0. In distinction that of 3T3 fibroblasts
transformed to the malignant state by Kirsten murine sarcoma virus and
MSU-1.1 cells transformed by transfection of the v-Ki-ras or T24 H-ras
oncogene was 6.1. These measurements suggest that ras transformation
results in a significant perturbation of lysosomal pH.
Alkalinization of the lysosomes is correlated with ras transformation of murine and human fibroblasts
Department of Biochemistry, Michigan State University, East Lansing 48824-1316.
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