Abstract
Fibroblasts derived from patients with I-cell disease have been shown to accumulate many natural substrates including a three to fourfold increase in sialic acid content compared to that found in normal fibroblasts. This diverse accumulation of storage material is due to a massive deficiency of multiple lysosomal hydrolases as they are preferentially excreted into the culture fluid. There is evidence that the I-cell plasma membrane itself is abnormal with respect to certain transferase activities and in its sensitivity to freezing and Triton X-100. In this study, we have shown that a neuraminidase-sensitive substrate, and perhaps others in I-cell fibroblasts, contribute to an increased electronegativity of the I-cell fibroblast surface and to the cells' sensitivity to freezing. We also found that neuraminidase treatment of I-cell fibroblasts before preservative freezing in liquid nitrogen enables the cells to adapt more easily to subculture upon thawing.
| Original language | English |
|---|---|
| Pages (from-to) | 588-592 |
| Number of pages | 5 |
| Journal | In Vitro |
| Volume | 17 |
| Issue number | 7 |
| DOIs | |
| State | Published - Jul 1981 |
Keywords
- cell electrophoresis
- cryopreservation
- I-cell disease
- neuraminidase
- sialic acid
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