Abstract | BACKGROUND: In cultured fibroblasts from I-cell disease patients the transport of many lysosomal enzymes is defective, and affected cells contain inclusion bodies filled with undegraded substrates. However, the contents of these inclusion bodies have not been well characterized yet. We attempted to identify accumulated substances in cultured I-cell disease fibroblasts cytochemically. METHODS: RESULTS: The patients' cells were granularly stained with the antibody to GM2 ganglioside and the lectins including Maakia amurensis, Datura stramonium, and concanavalin A. Their localization was coincident with that of LAMP-1. CONCLUSIONS:
|
Authors | Ikuo Kawashima, Mai Ohsawa, Tomoko Fukushige, Yoshihisa Nagayama, Yo Niida, Masaharu Kotani, Youichi Tajima, Takuro Kanekura, Tamotsu Kanzaki, Hitoshi Sakuraba |
Journal | Clinica chimica acta; international journal of clinical chemistry
(Clin Chim Acta)
Vol. 378
Issue 1-2
Pg. 142-6
(Mar 2007)
ISSN: 0009-8981 [Print] Netherlands |
PMID | 17204262
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
|
Chemical References |
- LAMP1 protein, human
- Lectins
- Lysosomal Membrane Proteins
- G(M2) Ganglioside
|
Topics |
- Cells, Cultured
- Female
- Fibroblasts
(chemistry)
- G(M2) Ganglioside
(analysis)
- Histocytochemistry
- Humans
- Infant
- Lectins
(analysis)
- Lysosomal Membrane Proteins
(analysis)
- Lysosomes
(enzymology)
- Microscopy, Electron
- Mucolipidoses
(metabolism, pathology)
- Skin
(ultrastructure)
|