Jain R K, Koenig G C, Dellian M, Fukumura D, Munn L L, Melder R J
Steele Laboratory, Department of Radiation Oncology, Massachusetts General Hospital, Boston, USA.
Cancer Metastasis Rev. 1996 Jun;15(2):195-204. doi: 10.1007/BF00437472.
Leukocyte-endothelial adhesion and angiogenesis, until recently considered as separate processes, have been shown to be linked by two recent findings: soluble cellular adhesion molecules (CAMs) involved in leukocyte-endothelial interactions are angiogenic and well known angiogenic molecules secreted by cancer or immune. cells can modulate the endothelial CAMs. This molecular link may partially explain why the overall leukocyte-endothelial interaction is often low and heterogeneous in angiogenic tumor vessels and why activated lymphocytes adhere nonuniformly to tumor vessels when injected into the tumor's blood supply.
白细胞与内皮细胞的黏附以及血管生成,直到最近还被认为是两个独立的过程,但最近的两项发现表明它们之间存在联系:参与白细胞与内皮细胞相互作用的可溶性细胞黏附分子(CAMs)具有血管生成作用,并且癌症或免疫细胞分泌的众所周知的血管生成分子可以调节内皮CAMs。这种分子联系可能部分解释了为什么在血管生成性肿瘤血管中白细胞与内皮细胞的总体相互作用通常较低且不均匀,以及为什么激活的淋巴细胞注入肿瘤血液供应时会不均匀地黏附于肿瘤血管。