Function of stromal cell and follicular dendritic cells on the functional differentiation and formation of lymph node
Function of stromal cell and follicular dendritic cells on the functional differentiation and formation of lymph node
批准号:
14570007
负责人:
YOSHIDA Toshiko
金额:
$2.24万
依托单位国家:
日本
项目类别:
Grant-in-Aid for Scientific Research (C)
财政年份:
2002
资助国家:
日本
项目状态:
已结题
起止时间:
2002 至 2003
中文摘要
利用IL-2受体γ链敲除小鼠,研究其与基质细胞和滤泡树突状细胞的关系,认为基质细胞和树突状细胞影响淋巴结结构和微环境的调节。用电子显微镜观察了其超微结构。采用单克隆抗体检测细胞的特异性,即MOMA-1、MOMA-2、TCR-β链、CD45R、MIDC-8、FDC-M1、FDC-M2进行免疫组化。IL-2 Rγ链不导致TcRβ(+) T细胞数量减少,但导致淋巴结和脾脏中CD45R(+) B细胞数量减少。即使淋巴结结构不完整,也不影响位于T细胞区的MIDC-8阳性树突状细胞。单核细胞增多,脾脏中MOMA-1(+)细胞消失,淋巴结中MOMA-1(+)细胞增多。在该小鼠的一组基质细胞中发现了FDCs的前体。由于抗原刺激后,淋巴细胞间出现典型的FDC细胞质伸长过程。B细胞在未成熟FDC向成熟FDC的分化过程中未起关键作用。将IL-2R小鼠间质细胞分别培养为记忆T细胞、记忆B细胞和免疫复合物。当我们使用从T细胞区和B细胞区难以分离的未成熟淋巴结中分离FDC的方法时,我们可以得到前体细胞,结果表明IL-2受体γ链可能在FDC的分化过程中不起关键作用。该模型对间质细胞的功能构建、微环境和FDC的研究具有重要意义。
英文摘要
The relationship with stromal cells and follicular dendritic cells, which are considered to influence the structure of lymph node and the adjustment of microenvironment, was investigated used by IL-2 receptorγ chain knockout mouse.We had observed the ultrastructure by the electron microscopy. And the peculiar characteristic for the cell was detected by using monoclonal antibody, that is MOMA-1,MOMA-2,TCR-β chain,CD45R,MIDC-8,FDC-M1 and FDC-M2, for immuno histochemistry.1.The IL-2 Rγ chain did not lead the decrease the numbers of TcRβ(+) T cells, but decrease CD45R(+) B cells in the lymph node and spleen. It dose not influence the MIDC-8 positive dendritic cells which were located in the T cell area even if the structure of lymph node is not complete. The numbers of monocyte were increased, but MOMA-1(+) cells in spleen were disappeared, but much ones in lymph node. Precursor of FDCs was included in a group of stromal cells in this mouse. Because after the stimulation by the antigen, there was observed typical FDC elongated cytoplasmic processes with antigens between lymphocytes. The B cell did not play critical role to differentiate from immature FDC to mature.2.The stromal cells separated from IL-2R KO mouse were cultured with memory T cell, memory B cell and immune complexes. When we used the method of the separation FDC from immature lymph node which is difficult to separate from T cell areas and B cell area, we could get the precursor cellsOur result suggested that IL-2 receptorγ chain may do not play critical roles on the differentiation of FDC. This model is very useful for investigation of functional construction and microenvironment of stromal cells and FDC.
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