ROLE OF CYTOPLASMIC ATP IN THE RESTORATION AND MAINTENANCE OF A MEMBRANE-PERMEABILITY BARRIER IN TRANSFORMED MAMMALIAN-CELLS

被引:25
作者
MAKAN, NR
机构
[1] Section of Biochemistry, Cornell University, Ithaca, New York, 14853, Wing Hall
关键词
D O I
10.1002/jcp.1041010314
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Addition of ATP to medium surrounding intact, transformed 3T3 cells activates the formation of aqueous channels in the plasma membrane. This results in efflux of nucleotide pools and ions and entry into the cytosol of charged, phosphorylated species. In such permeabilized cells, glycolysis is totally dependent on the external addition of glucose, inorganic phosphate, ADP, K+, Mg2+ and NAD+ which restore lactic acid formation to levels found in untreated cells. As expected, such reconstitution of glycolytic activity is found to restore intracellular ATP levels. This is accompanied by sealing of the membrane channels so that efflux of nucleotide pools ceases. Pyruvate, a substrate for mitochondrial ATP synthesis, when provided along with ADP and inorganic phosphate also produces sealing of the membrane channels. On the other hand, reactivation of pentose phosphate shunt activity, which does not lead to ATP synthesis, does not induce restoration of the membrane permeability barrier. Furthermore, compounds which lower the internal ATP pool prevent sealing, and also render the plasma membrane more sensitive to external ATP (Roxengurt and Heppel, 1979). Sealing of aqueous channels following restoration of the internal ATP pool is associated with phosphorylation of the inner membrane surface, and is unaffected by inhibitors of protein synthesis, microfilament or microtubular assembly. These results indicate the probable role of intracellular ATP in the restoration and/or maintenance of an active membrane barrier against efflux of small molecules and ions in transformed 3T3 cells. Copyright © 1979 Wiley‐Liss, Inc.
引用
收藏
页码:481 / 492
页数:12
相关论文
共 34 条
[1]   PHOSPHORYLATION AND DEPHOSPHORYLATION OF RENAL BRUSH-BORDER MEMBRANES BY PROTEIN KINASE AND PHOSPHOPROTEIN PHOSPHATASE [J].
ABOUISSA, H ;
MENDICINO, J ;
LEIBACH, F ;
PILLION, D .
FEBS LETTERS, 1975, 50 (02) :121-124
[2]   (P-32) PHOSPHORYL TRANSFER BY ENDOGENOUS PROTEIN KINASE AT GLIA AND GLIOMA CELL-SURFACE IN CULTURE INTO EXTRINSIC ACCEPTOR PROTEINS [J].
AGREN, G ;
RONQUIST, G .
ACTA PHYSIOLOGICA SCANDINAVICA, 1974, 92 (03) :430-432
[3]   LEAKAGE AS SOURCE OF OVERGROWTH STIMULATING ACTIVITY IN ROUS SARCOMA TRANSFORMED CULTURES [J].
BISSELL, MJ ;
RUBIN, H ;
HATIE, C .
EXPERIMENTAL CELL RESEARCH, 1971, 68 (02) :404-&
[4]   PLASMA-MEMBRANE PROTEIN-KINASE ACTIVITY IN NORMAL AND ROUS-SARCOMA VIRUS-TRANSFORMED CHICK-EMBRYO FIBROBLASTS [J].
BRANTON, PE ;
LANDRYMAGNAN, J .
BIOCHIMICA ET BIOPHYSICA ACTA, 1978, 508 (02) :246-259
[5]   RAPID METHOD FOR ISOLATION OF L-CELL SURFACE MEMBRANES USING AN AQUEOUS 2-PHASE POLYMER SYSTEM [J].
BRUNETTE, DM ;
TILL, JE .
JOURNAL OF MEMBRANE BIOLOGY, 1971, 5 (03) :215-&
[6]  
BUSCH H, 1962, INTRO BIOCH CANCER C, P356
[7]   EFFECT OF METABOLIC DEPLETION ON MEMBRANE-PERMEABILITY OF SMOOTH MUSCLE-CELLS AND ITS MODIFICATION BY LA3+ [J].
CASTEELS, R ;
VANBREEM.C ;
WUYTACK, F .
NATURE-NEW BIOLOGY, 1972, 239 (95) :249-&
[8]   GROWTH ON ARTIFICIAL MEDIUM OF AN AGENT ASSOCIATED WITH ATYPICAL PNEUMONIA AND ITS IDENTIFICATION AS A PPLO [J].
CHANOCK, RM ;
HAYFLICK, L ;
BARILE, MF .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1962, 48 (01) :41-&
[9]  
CHIANG TM, 1978, FED PROC, V37, P1328
[10]   ACTIVATION BY ADENOSINE 3'-5'-MONOPHOSPHATE OF A MEMBRANE-BOUND PHOSPHOPROTEIN PHOSPHATASE FROM TOAD BLADDER [J].
DELORENZO, RJ ;
GREENGARD, P .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1973, 70 (06) :1831-1835