Jonasson L, Bondjers G, Hansson G K
J Lipid Res. 1987 Apr;28(4):437-45.
The localization of lipoprotein lipase (LPL) in human atherosclerotic lesions was studied with immunocytochemical techniques. In the fibrous cap and surrounding intima of the plaque, where the smooth muscle cell is the dominating cell type, a high number of cells reacted with anti-LPL. A much lower number of stained cells was seen in the central lipid core region where the macrophages dominate. Further characterization of the LPL-containing cells in tissue sections showed that most of them were smooth muscle cells. Only a minor fraction of the macrophages in the plaque contained the enzyme. The results were confirmed on isolated cells from atherosclerotic tissue. Lipoprotein lipase was also detected in smooth muscle cells of non-atherosclerotic arteries. These findings suggest that the smooth muscle cells are the major source of LPL in the vascular wall. However, the enzyme was not present in some of the smooth muscle cells in the atherosclerotic lesion. This may imply that LPL synthesis is down-regulated in the atherosclerotic plaque.
采用免疫细胞化学技术研究了脂蛋白脂肪酶(LPL)在人类动脉粥样硬化病变中的定位。在斑块的纤维帽和周围内膜中,平滑肌细胞是主要的细胞类型,大量细胞与抗LPL发生反应。在巨噬细胞占主导的中央脂质核心区域,染色细胞的数量要少得多。对组织切片中含LPL细胞的进一步表征表明,其中大多数是平滑肌细胞。斑块中的巨噬细胞只有一小部分含有该酶。在从动脉粥样硬化组织分离出的细胞上证实了这些结果。在非动脉粥样硬化动脉的平滑肌细胞中也检测到了脂蛋白脂肪酶。这些发现表明,平滑肌细胞是血管壁中LPL的主要来源。然而,动脉粥样硬化病变中的一些平滑肌细胞中不存在该酶。这可能意味着动脉粥样硬化斑块中LPL的合成被下调。