UPTAKE OF INJECTED I-125 RICIN BY RAT-LIVER INVIVO - SUBCELLULAR-DISTRIBUTION AND CHARACTERIZATION OF THE INTERNALIZED LIGAND

被引:20
作者
FRENOY, JP [1 ]
TURPIN, E [1 ]
JANICOT, M [1 ]
GEHINFOUQUE, F [1 ]
DESBUQUOIS, B [1 ]
机构
[1] HOP NECKER ENFANTS MALAD, INSERM, U30, F-75730 PARIS 15, FRANCE
关键词
D O I
10.1042/bj2840249
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Subcellular-fractionation techniques were used to characterize the endocytic pathway followed by ricin in rat liver in vivo and tentatively identify the site(s) at which the ricin interchain disulphide bridge is split. After injection of I-125-ricin, hepatic uptake of radioactivity was maximum at 30 min (40% of injected dose). At 5 min, about 80% of the radioactivity in the homogenate was recovered in the microsomal (P) fraction, but later on the recovery of the radioactivity in the mitochondrial-lysosomal (ML) fractions progressively increased (50% at 30 min) at the expense of that in the P fraction. Subfractionation of the P and ML fractions on analytical sucrose-density gradients revealed a time-dependent translocation of the radioactivity from low- to high-density endocytic structures, with median relative densities at 5 and 60 min of about 1.15 and 1.16 (P fraction) and 1.19 and 1.22 (ML fraction) respectively. The late distribution of the radioactivity in the ML fraction was similar to that of the lysosomal marker acid phosphatase. Studies with co-injected lactose and mannan showed that ricin was internalized mainly via the mannose receptor. In the presence of mannan, the late recovery of radioactivity in the ML fraction was decreased, and the distribution of the radioactivity associated with the P fraction was shifted toward lower densities (median relative density 1.13), indicating a different pathway of endocytosis. Analysis of the radioactivity associated with the ML and S fractions by SDS/PAGE revealed a time-dependent increase in the amount of intact A- and B-chains and low-molecular-mass products. When ML fractions containing partially processed ricin were incubated at 37-degrees-C at pH 5 or at pH 7.2 in the presence of ATP, only low-molecular-mass products were generated. We conclude that internalized ricin associates with endocytic structures whose size and density of equilibration increase with time, and that, although detectable in these structures, reduction of the ricin interchain disulphide bridge occurs to a large extent in the cytosol.
引用
收藏
页码:249 / 257
页数:9
相关论文
共 64 条
  • [1] Aronson N N Jr, 1974, Methods Enzymol, V31, P90
  • [2] BAENZIGER JU, 1979, J BIOL CHEM, V254, P9795
  • [3] RICIN - TOXIC PROTEIN OF CASTOR-OIL SEEDS
    BALINT, GA
    [J]. TOXICOLOGY, 1974, 2 (01) : 77 - 102
  • [4] REDUCTION OF RICIN AND OTHER PLANT TOXINS BY THIOL-PROTEIN DISULFIDE OXIDOREDUCTASES
    BARBIERI, L
    BATTELLI, MG
    STIRPE, F
    [J]. ARCHIVES OF BIOCHEMISTRY AND BIOPHYSICS, 1982, 216 (01) : 380 - 383
  • [5] ANALYTICAL STUDY OF MICROSOMES AND ISOLATED SUBCELLULAR MEMBRANES FROM RAT-LIVER .1. BIOCHEMICAL METHODS
    BEAUFAY, H
    AMARCOST.A
    FEYTMANS, E
    THINESSE.D
    WIBO, M
    ROBBI, M
    BERTHET, J
    [J]. JOURNAL OF CELL BIOLOGY, 1974, 61 (01) : 188 - 200
  • [6] CALAFAT J, 1988, CANCER RES, V48, P3822
  • [7] TISSUE FRACTIONATION STUDIES .6. INTRACELLULAR DISTRIBUTION PATTERNS OF ENZYMES IN RAT-LIVER TISSUE
    DUVE, CD
    PRESSMAN, BC
    GIANETTO, R
    WATTIAUX, R
    APPELMANS, F
    [J]. BIOCHEMICAL JOURNAL, 1955, 60 (1-4) : 604 - 617
  • [8] SEPARATION OF RICIN A-CHAINS AND B-CHAINS AFTER DITHIOTHREITOL REDUCTION
    EMMANUEL, F
    TURPIN, E
    ALFSEN, A
    FRENOY, JP
    [J]. ANALYTICAL BIOCHEMISTRY, 1988, 173 (01) : 134 - 141
  • [9] ENDO Y, 1987, J BIOL CHEM, V262, P8128
  • [10] ENDO Y, 1987, J BIOL CHEM, V262, P5908