Reduced capacity of dendritic cells from trauma-hemorrhage mice in initiating delayed-type hypersensitivity to fluorescein isothiocyanate.

Reduced capacity of dendritic cells from trauma-hemorrhage mice in initiating delayed-type hypersensitivity to fluorescein isothiocyanate.
复制标题

创伤出血小鼠的树突状细胞引发异硫氰酸荧光素迟发型超敏反应的能力降低。

DOI:
10.3760/cma.j.issn.1008-1275.2009.06.003
复制
发表时间:
2009
期刊:
Chinese journal of traumatology = Zhonghua chuang shang za zhi
影响因子:
--
通讯作者:
Hua
Hua
中科院分区:
--
文献类型:
--
作者:
Hui Qiu;Sheng;Yong;Hua

文献摘要

参考文献

相似文献

OBJECTIVE To study the role of dendritic cells (DCs) in initiating delayed-type hypersensitivity (DTH) to fluorescein isothiocyanate (FITC) after trauma-hemorrhage in mice. METHODS Inbred BALB/c mice (6-8 weeks old, male) were epicutaneously sensitized with FITC 12 hours, 1 day, 2 days, 4 days and 7 days after closed bilateral femur fractures combined with hemorrhage. And 5 days after sensitization, DTH was evaluated by ear swelling after a challenge of FITC. Draining lymph node cells were examined for the percentages of FITC-positive cells, cluster of differentiation (CD)11c-positive cells and major histocompatibility complex II (MHC II)-positive cells by means of flow cytometry. In vitro proliferative responses of syngeneic lymphocytes and in vivo passive transfer of DTH to naive recipients induced by isolated DCs from the draining lymph nodes were determined. RESULTS The time of DTH to FITC decreased more significantly in the mice with trauma-hemorrhage (12 hours to 4 days) than in the mice with sham injury. After sensitization, the relative percentages of FITC+ cells, FITC+/CD11c+ cells and FITC+/CD11c+/MHC II+ cells from the draining lymph nodes were all significantly reduced following injury. And the capacity of DCs from the draining lymph nodes in stimulating proliferative responses of lymphocytes and transferring DTH to naive recipients were also inhibited after injury. CONCLUSIONS Trauma-hemorrhage induces repressive DTH in mice, which may be attributed, at least partially, to the reduced trafficking of DCs into the draining lymph nodes and insufficient maturation during DC migration.
DOI: 10.1152/ajpcell.00447.2008
发表时间: 2009-01-01
影响因子: 5.5
作者:
Kawasaki, Takashi;Choudhry, Mashkoor A.;Chaudry, Irshad H.
通讯作者: Chaudry, Irshad H.