Asano T, Matsushima K, Kleinerman E S
Department of Cell Biology, University of Texas M.D. Anderson Cancer Center, Houston 77030.
Cancer Immunol Immunother. 1994 Jan;38(1):16-22. doi: 10.1007/BF01517165.
Liposome-encapsulated muramyl tripeptide phosphatidylethanolamine (L-MTP-PE) is a novel immune modulator that is now under investigation against metastatic melanoma and osteosarcoma. We have already reported that L-MTP-PE induced monocyte-mediated tumoricidal activity and up-regulation of the tumor necrosis factor and interleukin-1 (IL-1) in vivo and in vitro. We now demonstrate that L-MTP-PE also induces monocyte chemotactic and activating factor (MCAF) mRNA expression at both the transcriptional and post-transcriptional levels. Monocyte chemotactic activity was also present in the supernatants of L-MTP-PE-stimulated cells. In monocytes, the increased expression of MCAF was induced rapidly (by 2 h) but was short-lived. By 4 h, MCAF mRNA had decreased to background level. We found no change in MCAF mRNA levels in lymphocytes exposed to L-MTP-PE. We therefore conclude that L-MTP-PE selectively up-regulates MCAF expression in monocytes and that MCAF may play a role in the tumoricidal and immune-stimulating activity of L-MTP-PE.
脂质体包裹的胞壁酰三肽磷脂酰乙醇胺(L-MTP-PE)是一种新型免疫调节剂,目前正针对转移性黑色素瘤和骨肉瘤进行研究。我们已经报道过,L-MTP-PE在体内和体外均可诱导单核细胞介导的杀瘤活性以及肿瘤坏死因子和白细胞介素-1(IL-1)的上调。我们现在证明,L-MTP-PE在转录和转录后水平均能诱导单核细胞趋化和激活因子(MCAF)mRNA表达。L-MTP-PE刺激的细胞上清液中也存在单核细胞趋化活性。在单核细胞中,MCAF的表达增加迅速(2小时内),但持续时间较短。到4小时时,MCAF mRNA已降至背景水平。我们发现暴露于L-MTP-PE的淋巴细胞中MCAF mRNA水平没有变化。因此,我们得出结论,L-MTP-PE选择性地上调单核细胞中MCAF的表达,并且MCAF可能在L-MTP-PE的杀瘤和免疫刺激活性中发挥作用。