Distribution of bone-marrow-derived endothelial and immune cells in a murine colitis-associated colorectal cancer model.
Distribution of bone-marrow-derived endothelial and immune cells in a murine colitis-associated colorectal cancer model.
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小鼠结肠炎相关结直肠癌模型中骨髓源性内皮细胞和免疫细胞的分布
DOI:
10.1371/journal.pone.0073666
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发表时间:
2013
期刊:
影响因子:
3.7
通讯作者:
Guleng B
中科院分区:
文献类型:
--
作者:
Xiao CX;Wang HH;Shi Y;Li P;Liu YP;Ren JL;Guleng B
Inflammatory bowel disease (IBD) can lead to an increased risk of developing colorectal cancer (CRC). The aim of this study was to establish a model for combined bone marrow transplantation (BMT) and colitis-associated colorectal cancer (CAC) and to define the contribution of BM-derived cells during the inflammation associated with carcinogenesis. We established a model for BMT using green fluorescent protein (GFP) transgenic mice, followed by AOM/DSS-induced CAC, and performed confocal microscopy analysis on in vivo living tissue and frozen tumor sections. Our imaging analyses showed that GFP-positive cells extensively infiltrated the tumor stroma and that some WGA and GFP or CD31 and GFP double-positive cells were observed in the lining of tumor vessels. Flow cytometry analysis of the tumor-infiltrating cells showed that the GFP-positive CD11c+ DCs cells were one-third of the GFP+/CD11C- cells, and that half of these DCs (0.96% vs 1.02%) were GFP-positive BM-derived cells. The majority of CD4+ T cells were GFP-negative (12.02% vs 1.9%), and we discovered a novel CD4+ CD11c+ DC subset (0.34% vs 1.64%). In conclusion, we defined the distribution of BM-derived endothelial cells, CD11c+ DCs and CD4+ T cells in tumors. This model might be useful for elucidating the diverse BM-derived cell types and functions during the progression of colitis-associated colorectal cancer.
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影响因子:
0.7
作者:
Laurent, Julien;Touvrey, Cedric;Ruegg, Curzio
通讯作者:
Ruegg, Curzio
影响因子:
11.2
作者:
Guleng, B;Tateishi, K;Omata, M
通讯作者:
Omata, M
影响因子:
3.2
作者:
Ferrara, Napoleone
通讯作者:
Ferrara, Napoleone
影响因子:
82.9
作者:
Okamoto, R;Yajima, T;Watanabe, M
通讯作者:
Watanabe, M
影响因子:
4.4
作者:
Brinster, C;Shevach, EM
通讯作者:
Shevach, EM