Lysosomal enzymes inhibit binding of insulin-like growth factor II (IGF-II) to the IGF-II/mannose-6-phosphate receptor

1989 ◽  
Vol 120 (3_Suppl) ◽  
pp. S192
Author(s):  
W. KIESS ◽  
C. THOMAS ◽  
M. SKLAR ◽  
G. SAHAGIAN ◽  
S. P. NISSLEY
Keyword(s):  
Growth Factor ◽  
Lysosomal Enzymes ◽  
Insulin Like Growth Factor ◽  
Factor Ii ◽  
Mannose 6 Phosphate

Mannose 6-phosphate Receptor (MPR 300) Proteins from Goat and Chicken Bind Human IGF-II

2006 ◽  
Vol 26 (2) ◽  
pp. 101-112 ◽  
Author(s):  
Suresh Koduru ◽  
Sivaramakrishna Yadavalli ◽  
Siva Kumar Nadimpalli
Keyword(s):  
Plasma Membrane ◽  
Growth Factor ◽  
Lysosomal Enzymes ◽  
Growth Factor Receptor ◽  
Cell Receptor ◽  
Insulin Like Growth Factor ◽  
Fish Embryo ◽  
Multifunctional Protein ◽  
Factor Ii ◽  
Mannose 6 Phosphate

Mannose 6-phosphate receptor proteins (MPR 300 and 46) in mammals have been shown to mediate transport of lysosomal enzymes to lysosomes intracellularly. Both receptors are also expressed on the plasma membrane. Only MPR 300 protein on the plasma membrane has been shown to be a multifunctional protein which in addition to binding mannose 6-phosphate containing proteins also binds human insulin-like growth factor-II (IGF-II) causing its internalization [Hille-Rehfeld, A. (1995) Mannose 6-phosphate receptors in sorting and transport of lysosomal enzymes. Biochim. Biophys. Acta. 1241: 177–194]. This property has been shown to be exhibited by other mammalian receptors but not by the chicken and frog receptors. In a recent study however it was shown that the fish embryo MPR 300 binds human IGF-II. [Mendez, E., Planas, J.V., Castillo, J., Navarro, I. and Gutierrez, J. (2001) Identification of a type II insulin-like growth factor receptor in fish embryos. Endocrinology, 142: 1090–1097]. In the present study, we demonstrate that the purified goat and chicken liver receptors bind human IGF-II by employing cross-linking experiments (purified receptors and radiolabeled IGF-II) and by ligand blotting (using purified receptors and biotinylated IGF-II). Further CEF cells (chicken embryonic fibroblasts) that are known to contain the putative MPR 300 protein were employed to demonstrate that the CEF cell receptor binds human IGF-II.

scholarly journals Mouse mutants lacking the cation-independent mannose 6-phosphate/insulin-like growth factor II receptor are impaired in lysosomal enzyme transport: comparison of cation-independent and cation-dependent mannose 6-phosphate receptor-deficient mice

1998 ◽  
Vol 330 (2) ◽  
pp. 903-908 ◽  
Author(s):  
Istvan SOHAR ◽  
David SLEAT ◽  
Chang-Gong LIU ◽  
Thomas LUDWIG ◽  
Peter LOBEL
Keyword(s):  
Growth Factor ◽  
Lysosomal Enzyme ◽  
Enzyme Activities ◽  
Lysosomal Enzymes ◽  
Insulin Like Growth Factor ◽  
Factor Ii ◽  
Solid Tissues ◽  
Mannose 6 Phosphate ◽  
Deficient Mice

Two proteins have been implicated in the mannose 6-phosphate-dependent transport of lysosomal enzymes to lysosomes: the 300 kDa cation-independent and the 46 kDa cation-dependent mannose 6-phosphate receptors (CI- and CD-MPRs). The mammalian CI-MPR also mediates endocytosis and clearance of insulin-like growth factor II (IGF-II). Mutant mice that lack the CD-MPR are viable, mice that lack the CI-MPR accumulate high levels of IGF-II and usually die perinatally, whereas mice that lack both IGF-II and CI-MPR are viable. To investigate the relative roles of the MPRs in the targeting of lysosomal enzymes in vivo, we analysed the effect of a deficiency of either MPR on lysosomal enzyme activities in animals lacking IGF-II. In CD-MPR-deficient mice, most activities were relatively normal in solid tissues and some were marginally elevated in serum. In CI-MPR-deficient mice, some enzyme activities were moderately decreased in solid tissues and multiple enzymes were markedly elevated in serum. Finally, total levels of serum mannose 6-phosphorylated glycoproteins were ~ 45-fold and ~ 15-fold higher than wild type in CI- and CD-MPR-deficient mice respectively, and there were specific differences in the pattern of these proteins when comparing CI- and CD-MPR deficient animals. These results indicate that while lack of the CI-MPR appears to perturb lysosome function to a greater degree than lack of the CD-MPR, each MPR has distinct functions for the targeting of lysosomal enzymes in vivo.

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