Bobryshev Y V, Lord R S
St. Vincent's Hospital, University of New South Wales, Sydney, Australia.
J Submicrosc Cytol Pathol. 1996 Jan;28(1):49-60.
Structural heterogeneity and contact interactions of vascular dendritic cells (VDCs) in early atherosclerotic lesions of the human aortic intima were studied using electron microscopy. VDCs were identified through their ultrastructural features which were typical of dendritic cells. From their morphological characteristics, two phenotypes of VDCs (types I and II) were distinguished. VDCs were found to be distributed throughout atherosclerotic lesions, and through their processes were seen to be in contact with each other and with other intimal cells. VDCs developed multiple contacts with intimal macrophages, smooth muscle cells and foam cells. Smooth muscle cells contacting VDCs were mainly of synthetic phenotype suggesting the involvement of VDCs in the regulation of cell phenotypes. Occasionally, contacts between VDCs and lymphocyte-like cells were also observed. We speculate that through cell-to-cell contacts, VDCs are involved in immune reactions in atherosclerotic lesions.
利用电子显微镜研究了人主动脉内膜早期动脉粥样硬化病变中血管树突状细胞(VDCs)的结构异质性和接触相互作用。通过树突状细胞典型的超微结构特征鉴定出VDCs。根据其形态特征,区分出两种表型的VDCs(I型和II型)。发现VDCs分布于整个动脉粥样硬化病变中,通过其突起可见它们相互接触并与其他内膜细胞接触。VDCs与内膜巨噬细胞、平滑肌细胞和泡沫细胞形成多种接触。与VDCs接触的平滑肌细胞主要为合成表型,提示VDCs参与细胞表型的调节。偶尔也观察到VDCs与淋巴细胞样细胞之间的接触。我们推测,通过细胞间接触,VDCs参与动脉粥样硬化病变中的免疫反应。