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   <subfield code="a">Monoclonal antibodies against human chondrocytes</subfield>
   <subfield code="h">[Elektronische Daten]</subfield>
   <subfield code="c">[J. Bujia, M. Sittinger, H. Sudhoff, A. Fisseler-Eckhoff, G. Burmester, E. Kastenbauer, C. Hammer]</subfield>
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   <subfield code="a">Summary: Cell-specific antigens are mainly found in cells or membrane surfaces rather than in the surrounding matrix. However, until now it was not possible to produce antibodies specific for cellular structures of chondrocytes. In 1989, Lance (Immunol. Lett. 21:63-73; 1989) first established specific monoclonal antibodies for human articular chondrocytes tested only by immunofluorescence. Studies describing the specificity of these five antibodies (HUMC 1-5) and their relevance for immunohistological analysis of cartilage tissue were not available until now. Therefore, the aim of the following study was to investigate the distribution of HUMC 1, 2, 3, 4, and 5 in mesenchymal cellsin vivo andin vitro immunohistochemically. Further investigations concentrate on the localization of chondrocyte specific antigens using immunoelectron microscopy. Immunohistological studies showed positive immunostainings with all five antibodies in human chondrocytesin vivo andin vitro. A cross-reaction with human fibroblasts and osteoblasts for the antibodies HUMC 2 and HUMC 5 was observed. furthermore, a parallel loss of immunoreactivity for HUMC 1, HUMC 3, and HUMC 4 was observed in cultured chondrocytes indicating that the specific antigens vanish during differentiation observedin vitro. Subsequent immunoblot analysis employing collagens as antigens did not show any reactivity. Using immunoelectron microscopy, gold particle labeling was observed in intracytoplasmatic vesicles of isolated chondrocytes. Our results indicate that HUMC 1, HUMC 3, and HUMC 4 are specific for cartilage cells and might be suitable for immunohistological analysis of different cartilage tissues and pathologically altered chondrocytes.</subfield>
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   <subfield code="a">Society for In Vitro Biology, 1996</subfield>
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   <subfield code="a">cartilage differentiation</subfield>
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   <subfield code="a">monoclonal antibodies</subfield>
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   <subfield code="a">Bujia</subfield>
   <subfield code="D">J.</subfield>
   <subfield code="u">Department of Otolaryngology, Ludwig-Maximilians-University of Munich, Germany</subfield>
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   <subfield code="a">Sittinger</subfield>
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   <subfield code="u">Department of Medicine III, Charité, Humboldt University of Berlin, Germany</subfield>
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   <subfield code="D">H.</subfield>
   <subfield code="u">Department of Otorhinolaryngology, St. Elisabeth Hospital, Germany</subfield>
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   <subfield code="a">Fisseler-Eckhoff</subfield>
   <subfield code="D">A.</subfield>
   <subfield code="u">Institute of Pathology, Berufsgenossenschaftliche Kliniken &quot;Bergmannsheil” University of Bochum, Germany</subfield>
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   <subfield code="u">Department of Medicine III, Charité, Humboldt University of Berlin, Germany</subfield>
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   <subfield code="u">Department of Otolaryngology, Ludwig-Maximilians-University of Munich, Germany</subfield>
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   <subfield code="t">In Vitro Cellular &amp; Developmental Biology - Animal</subfield>
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