Deficiency of mannose 6-phosphate receptors and lysosomal storage: a morphometric analysis of hepatocytes of neonatal mice

被引:5
作者
Schellens, JPM
Saftig, P
von Figura, K
Everts, V
机构
[1] Univ Amsterdam, Acad Med Ctr, Dept Cell Biol & Histol, NL-1100 DE Amsterdam, Netherlands
[2] Christian Albrecht Univ, Kiel, Germany
[3] Univ Gottingen, D-3400 Gottingen, Germany
[4] Acad Ctr Dent Amsterdam, Dept Periodontol, NL-1066 EA Amsterdam, Netherlands
[5] Acad Ctr Dent Amsterdam, Dept Oral Cell Biol, NL-1066 EA Amsterdam, Netherlands
关键词
neonatal mice; M6PR-deficient; hepatocytes; lysosomes; morphometric analysis;
D O I
10.1016/j.cellbi.2003.07.001
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Transport of lysosomal enzymes is mediated by two mannose 6-phosphate receptors: a cation dependent (CD-MPR) and a cation independent receptor (CI-MPR). In the present study the effect of MPR-deficiency on the lysosomal system of neonatal mouse hepatocytes was studied by ultrastructural morphometric analyses. The volume density of the lysosomal system in hepatocytes of mice that lack both receptors was significantly increased in comparison with controls and with mice deficient for CI-MPR only. This higher volume density was due to a nine-fold increase of residual bodies. In CI-MPR-deficient mice the volume density of the lysosomal system was not different from controls and no increase of residual bodies was observed. It is concluded that in hepatocytes of MPR-deficient neonatal mice lysosomal storage occurs when both MPRs are lacking, whereas deficiency of CI-MPR only has no effect on the ultrastructure of the lysosomal system. (C) 2003 Elsevier Ltd. All rights reserved.
引用
收藏
页码:897 / 902
页数:6
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