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J A Witkowski

Publications and source records attributed to J A Witkowski.

At least 145 records · Page 8Linked to original sources
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Tissue culture studies of muscle disorders: Part 1. Techniques, cell growth, morphology, cell surface.

Tissue culture has been used extensively in studies of human inherited disorders, and its application in the field of the neuromuscular disorders has increased rapidly in recent years. This review, covering the period 1977 to 1984, deals with tissue culture studies of both human and animal muscle disorders, although Duchenne muscular dystrophy (DMD) figures prominently because of the overwhelming interest in that disorder. The review is in two parts. In the first part, I discuss technical innovations in the field, the morphology and growth of cells, and a variety of studies related to the cell surface. Important findings in relation to DMD include reports of abnormal growth rates and reduced lifespan of DMD cells, hypersensitivity to DNA-damaging agents, abnormal cell-to-cell and cell-to-substratum adhesion, and a more "fluid" cell membrane. However, these findings are controversial or have so far been reported only by single laboratories.

Animals↗
PubMedDate not supplied

Rotation-mediated aggregation of skin fibroblasts in Duchenne muscular dystrophy. Effects of monensin.

Rotation-mediated aggregation of human skin fibroblasts has been studied and the patterns of aggregation compared between cultures obtained from 9 patients with Duchenne muscular dystrophy and from 10 normal controls. The rate of aggregation was dependent on the growth state of the cells, with growing cells aggregating more rapidly than growth-arrested cells. There was considerable variation between individuals in the rate at which cells aggregated but no differences were detected in the aggregation of normal and DMD cells measured by this method. The monovalent cation ionophore monensin, which inhibits the transport of cellular proteins to the extracellular medium, reduced aggregation of all cells. The data suggest that after initial cell-cell contact continued aggregation is dependent on the secretion of materials to the cell surface. The aggregation of normal and DMD cells was affected similarly by this treatment.

Adolescent↗
PubMedDate not supplied

Wound cleansers.

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Animals↗