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pubmed-article:7574467pubmed:abstractTextFragments of sural nerve biopsy specimens were cultured in the presence of the supernatant of lymphokine-activated killer cells, resulting in the selective outgrowth of cells with bipolar or tripolar morphology, reminiscent of that of Schwann cells. Immunofluorescent staining with antibodies to the S-100 protein, the low-affinity nerve growth factor receptor, and the surface Thy-1 antigen confirmed that these cultures contained more than 99% Schwann cells and no detectable fibroblasts. The mitotic activity of Schwann cells was measured by bromodeoxyuridine labeling, and was increased when the cells were grown in medium with lymphokine-activated killer cell supernatant compared with medium without this supernatant. In the presence of lymphokine-activated killer cell supernatant, Schwann cells could be maintained in continuous culture for a minimum of 8 months.lld:pubmed
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pubmed-article:7574467pubmed:authorpubmed-author:BärP RPRlld:pubmed
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pubmed-article:7574467pubmed:authorpubmed-author:WokkeJ JJJlld:pubmed
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pubmed-article:7574467pubmed:volume38lld:pubmed
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pubmed-article:7574467pubmed:pagination674-8lld:pubmed
pubmed-article:7574467pubmed:dateRevised2006-11-15lld:pubmed
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pubmed-article:7574467pubmed:year1995lld:pubmed
pubmed-article:7574467pubmed:articleTitleSelective expansion and long-term culture of human Schwann cells from sural nerve biopsies.lld:pubmed
pubmed-article:7574467pubmed:affiliationRudolf Magnus Research School in the Neurosciences, Department of Neurology, University Hospital Utrecht, Netherlands.lld:pubmed
pubmed-article:7574467pubmed:publicationTypeJournal Articlelld:pubmed
pubmed-article:7574467pubmed:publicationTypeResearch Support, Non-U.S. Gov'tlld:pubmed
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