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Differential expression of CD146 in tissues and endothelial cells derived from infantile haemangioma and normal human skin

CD146号 病理 免疫组织化学 内皮干细胞 生物 流式细胞术 周细胞 内皮 细胞粘附分子 免疫学 医学 川地34 细胞生物学 干细胞 内分泌学 体外 生物化学
作者
Qing Li,Ying Yu,Joyce Bischoff,John B. Mulliken,Bjørn R. Olsen
出处
期刊: 卷期号:201 (2): 296-302 被引量:102
标识
DOI:10.1002/path.1443
摘要

Abstract Haemangioma is the most common tumour of endothelial origin, occurring in 4–10% of Caucasian infants. It is characterized by rapid growth during the first year of postnatal life, followed by spontaneous regression from 1 to 7 years of age. The cell surface adhesion molecule CD146 has been identified as an endothelial cell marker. Despite advances in understanding the functional role of CD146 in normal endothelial cells and tumour progression, its expression and a possible role in an endothelial tumour have not been studied. As part of an investigation of endothelial cell alterations in infantile haemangioma, differential expression studies were performed with several known antigens and endothelial cell markers. Using immunohistochemical and flow cytometric analyses, cultured human dermal microvascular endothelial cells isolated from newborn foreskin (HDMEC) were compared with endothelial cells derived from haemangioma tissue (HemECs). In addition, immunohistochemistry was used to compare haemangioma tissues with normal human skin. Unexpectedly, cultured HemECs showed a significantly lower level of CD146 than HDMECs by both flow cytometric analysis and immunofluorescence staining. Using immunohistochemical studies, it was further demonstrated that endothelia in all haemangioma tissues, regardless of the tumour phase, showed negative immunoreactivity for CD146. In contrast, strong positive staining for CD146 was observed in the pericyte‐like cells that surround the endothelial layers. These findings are believed to be relevant to the molecular basis of haemangioma. Furthermore, it is possible that antibodies against CD146 may be useful for separating haemangioma‐derived endothelial cells from normal endothelial cells and pericytes. Copyright © 2003 John Wiley & Sons, Ltd.
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