Ramanathapuram Lalitha V, Hopkin Dustin, Kurago Zoya B
Oral and Maxillofacial Pathology, Radiology and Medicine, College of Dentistry, New York University, 345 E. 24th St., Rm 837S, 1010S, New York, NY, 10010, USA.
Cancer Microenviron. 2013 Apr;6(1):41-55. doi: 10.1007/s12307-011-0077-4. Epub 2011 Aug 2.
In the inflammatory mucosal microenvironment of head and neck SCC (HNSCC), DC express CD16 and are usually in direct contact with tumor cells. Mucosal and inflammation-associated DC develop from monocytes, and monocyte-derived DC are used in HNSCC immunotherapy. However, beyond apoptotic tumor cell uptake and presentation of tumor antigens by DC, HNSCC cell interactions with DC are poorly understood. Using co-cultures of monocyte-derived DC and two established HNSCC cell lines that represent well- and poorly-differentiated SCC, respectively, we found that carcinoma cells induced significant increases in CD16 expression on DC while promoting a CD1a(+)CD86(dim) immature phenotype, similar to that observed in HNSCC specimens. Moreover, HNSCC cells affected steady-state and CCL21-induced migration of DC, and these effects were donor-dependent. The CCL21-induced migration directly correlated with HNSCC-mediated effects on CCR7 and CD38 expression on DC-SIGN-high DC. The dominant pattern seen in six out of nine donors was the increase in steady-state and CCL21-induced DC migration in co-cultures with HNSCC, while the reverse pattern, i.e., decreased DC migration in co-cultures with SCC, was identified in two donors. A split in migratory DC behavior, i.e. increase with one HNSCC cell line and a decrease with the second cell line, was observed in one donor. Remarkably, the numbers of live detached HNSCC cells were orders of magnitude higher in DC-HNSCC co-cultures than in parallel HNSCC cell cultures without DC. This study provides novel insights into the effects of DC-HNSCC interactions relevant to the tumor microenvironment.
在头颈部鳞状细胞癌(HNSCC)的炎性黏膜微环境中,树突状细胞(DC)表达CD16,且通常与肿瘤细胞直接接触。黏膜及炎症相关的DC由单核细胞发育而来,单核细胞衍生的DC已应用于HNSCC免疫治疗。然而,除了DC摄取凋亡肿瘤细胞并呈递肿瘤抗原外,HNSCC细胞与DC之间的相互作用仍知之甚少。我们将单核细胞衍生的DC与两种已建立的HNSCC细胞系共同培养,这两种细胞系分别代表高分化和低分化的鳞状细胞癌,结果发现癌细胞可诱导DC上CD16表达显著增加,同时促进CD1a(+)CD86(dim)未成熟表型的形成,这与在HNSCC标本中观察到的情况相似。此外,HNSCC细胞影响DC的稳态迁移以及CCL21诱导的迁移,且这些效应具有供体依赖性。CCL21诱导的迁移与HNSCC对DC-SIGN高表达DC上CCR7和CD38表达的影响直接相关。在9名供体中,有6名供体的主要模式是与HNSCC共培养时稳态迁移和CCL21诱导的DC迁移增加,而在另外2名供体中则发现了相反的模式,即与鳞状细胞癌共培养时DC迁移减少。在1名供体中观察到迁移性DC行为出现分歧,即与一种HNSCC细胞系共培养时增加,而与另一种细胞系共培养时减少。值得注意的是,在DC-HNSCC共培养中,存活的脱落HNSCC细胞数量比没有DC的平行HNSCC细胞培养高出几个数量级。这项研究为与肿瘤微环境相关的DC-HNSCC相互作用的影响提供了新的见解。