RESUMO
Mannose 6-phosphate receptor deficient mice were generated by crossing mice carrying null alleles for Igf2 and the 300 kDa and 46 kDa mannose 6-phosphate receptors, Mpr300 and Mpr46. Pre- and perinatal lethality of mice nullizygous for Igf2, Mpr300 and Mpr46 was increased. Triple deficient mice surviving the first postnatal day had normal viability and developed a phenotype resembling human I-cell disease. The triple deficient mice were characterized by dwarfism, facial dysplasia, waddling gait, dysostosis multiplex, elevated lysosomal enzymes in serum and histological signs of lysosomal storage predominantly in fibroblasts, but also in parenchymal cells of brain and liver. A paternally inherited Mpr300 wild type allele that is normally inactive in mice due to imprinting was reactivated in some tissues of mice lacking IGF II and MPR 46 and carrying a maternal Mpr300 null allele. Inspite of the partial reactivation the phenotype of these mice was similar to that of triple deficient mice.
Assuntos
Mucolipidoses/genética , Receptor IGF Tipo 2/genética , Animais , Western Blotting , Osso e Ossos/diagnóstico por imagem , Feminino , Impressão Genômica , Genótipo , Heterozigoto , Lisossomos/enzimologia , Masculino , Camundongos , Mucolipidoses/diagnóstico por imagem , Mucolipidoses/patologia , Fenótipo , Radiografia , Receptor IGF Tipo 2/deficiênciaRESUMO
The cytoplasmic tail of the human 46 kDa mannose 6-phosphate receptor (MPR 46) is necessary for rapid internalization of the receptor and sufficient to mediate internalization of a resident plasma membrane protein. To localize the internalization sequences within the 67 amino acids of the cytoplasmic tail, the tail was progressively shortened from its C-terminus, internal deletions of between four and eight amino acids were introduced into the tail, and individual residues were substituted by alanine, glycine or serine. Three sequences were identified that contribute to the internalization of MPR 46. The first is located within the 23 juxtamembrane cytoplasmic residues of the tail. It contains four essential residues within a heptapeptide and does not resemble known internalization signals. The second sequence contains as a critical residue Tyr-45. The third region is located within the C-terminal seven residues and contains a di-leucine pair as essential residues. The first and third sequences were shown to function as autonomous internalization sequences. Substitution of critically important residues within a single internalization sequence was tolerated, with no or only a moderate decrease in the internalization rate. When essential residues from two or all three internalization sequences were substituted, however, the internalization rate was decreased by more than 60% and 90% respectively. This indicates that the autonomous internalization signals in the cytoplasmic tail of MPR 46 function in an additive manner, but are partly redundant.
Assuntos
Citoplasma/metabolismo , Manosefosfatos/metabolismo , Receptor IGF Tipo 2/química , Sequência de Aminoácidos , Linhagem Celular , Membrana Celular/metabolismo , Citoplasma/química , Endocitose , Fibroblastos , Genes Reporter , Humanos , Rim/citologia , Leucina/genética , Leucina/fisiologia , Dados de Sequência Molecular , Peso Molecular , Mutagênese Sítio-Dirigida , Peptídeos/metabolismo , Receptor IGF Tipo 2/genética , Deleção de Sequência , Tirosina/genética , Tirosina/fisiologiaRESUMO
Morphological and biochemical autopsy findings of a 12 year old girl with mucopolysaccharidosis type III (Sanfilippo's syndrome). The clinically suspected diagnosis was biochemically ascertained before the patients death. The autopsy findings obtained by biochemical and by light and electron microscopic investigations of different organs are compared with the results of other authors.