期刊文献+

脂多糖诱导的CD11b^+Gr-1^+髓源抑制性细胞对小鼠脾脏T细胞增殖的抑制作用 被引量:3

Inhibition of lipopolysaccharide-induced myeloid.derived suppressor cells in the proliferation of spleen T lymphocytes
原文传递
导出
摘要 目的观察脂多糖诱导的CD11b^+Gr-1^+髓源抑制性细胞(MDSCs)对小鼠脾脏T细胞增殖的影响,探讨其在免疫调控可能发挥的作用。方法10只6-8周龄BALB/c小鼠随机数字表法随机分为脂多糖组和对照组各5只,分别予脂多糖或生理盐水腹腔注射;采用CD11b磁珠从脾脏组织中分选MDSCs,通过瑞氏.姬姆萨染色观察细胞形态,并用流式细胞术检测细胞表面特征分子表达情况;四唑盐(MTr)比色法测定与MDSCs在体外共培养后T细胞的增殖情况。结果脂多糖组小鼠脾脏组织中CD11b^+Gr-1^+MDSCs比例为27.4%±6.6%,较对照组(5.1%±3.8%)明显增多(t=5.06,P=0.007);采用CD11b磁珠从注射脂多糖的小鼠脾脏中分离出的CD11b^+Gr-1^+MDSCs纯度高达84.0%±4.2%;MTr法显示在MDSCs共培养后脾脏T细胞增殖水平明显低于对照组,且此作用与MDSCs的数量呈正相关(F=46.26,P=0.000)。结论CD11b磁珠可分离提取出纯度较高的脂多糖来源的MDSCs,且脂多糖诱导的MDSCs对脾脏T细胞的增殖具有抑制作用,该作用呈剂量依赖性关系。 Objective To explore the effects of lipopolysaccharide (LPS) -induced myeloid-derived suppressor cells (MDSCs) on the proliferation of spleen T lymphocytes. Methods BALB/c mice were randomly divided into two groups: LPS group and normal control group. They were injected intraperitoneally with LPS and normal saline solution respectively. MDSCs were separated with CD1 lb immunomagnetic beads from the spleen extract of mice. The morphological characteristics of MDCSs were observed by Wright- Giemsa staining and the characteristic molecules on cell surface identified by flow cytometry. And the effects of MDSCs on the in vitro proliferation of T cells were determined by methylthiazolyldiphenyl-tetrazolium bromide (MTY). Results The proportion of MDSCs in the spleen of the LPS group was much more than that of the normal control group (27.4% ±6.6% vs5.1% ±3.8%; t=5.06, P=0.007). CD11b^+Gr-1^+ MDSCs could be separated by CDllb immunomagnetic beads from the spleen of mice injected with LPS at a high purity of 84.0% ±4. 2%. MTT method showed that the proliferation of T cells decreased significantly after a co-cultivation withCD11b^+Gr-1^+MDSCs versus the control group. And it was positively correlated with the number of MDSCs ( F = 46. 26, P = 0. 000). Conclusions A high purity of LPS-induced myeloid-derived suppressor cells may be separated with CD11 b immunomagnetic beads. And it has dose-dependent inhibitory effects on the proliferation of the spleen T lymphocytes.
出处 《中华医学杂志》 CAS CSCD 北大核心 2012年第24期1702-1705,共4页 National Medical Journal of China
基金 广东省科技计划项目(20108031600095)
关键词 脂多糖 T淋巴细胞 调节性 细胞增殖 Lipopolysacc-harides T-lymphocytes, regulatory Cell proliferation
  • 相关文献

参考文献14

  • 1Delano MJ, Scumpia PO, Weinstein JS, et al. MyD88-dependent expansion of an immature GR-1 + CD1 l b + population induces T cell suppression and Th2 polarization in sepsis. J Exp Med, 2007, 204 .. 1463-1474.
  • 2De Santo C, Salio M, Masri SH, et al. Invariant NKT cells reduce the immunosuppressive activity of influenza A virus-induced myeloid-derived suppressor cells in mice and humans. J Clin Invest, 2008, 118 : 4036-4048.
  • 3Makarenkova VP, Bansal V, Matta BM, et al. CD11b+/Gr-1+ myeloid suppressor ceils cause T cell dysfunction after traumatic stress. J Immunol, 2006, 176: 2085-2094.
  • 4Zhu B, Bando Y, Xiao S, et al. CD11b+ Ly-6Chi suppressive monocytes in experimental autoimmune encephalomyelitis. J Immunol, 2007, 179: 5228-5237.
  • 5Movahedi K, Guilliams M, Van den Bossche J, et al. Identification of discrete tumor-induced myeloid-derived suppressor cell subpopulations with distinct T cell-suppressive activity. Blood, 2008, 111 : 4233-4244.
  • 6Dugast AS, Handebourg T, Coulon F, et al. Myeloid-derived suppressor cells accumulate in kidney allograft tolerance and specifically suppress effector T cell expansion. J Immunol, 2008, 180 : 7898-7906.
  • 7Arora M, Poe SL, Oriss TB, et al. TLR4/MyD88-induced CD11b+ Gr-lint F4/80 + non-migratory myeloid cells suppress Th2 effector function in the lung. Mucosal Immunol, 2010, 3: 578-593.
  • 8De Wilde V, Van Rompaey N, Hill M, et al. Endotoxin-induced myeloid-derived suppressor cells inhibit alloimmune responses via heine oxygenase-1. Am J Transplant, 2009, 9 : 2034-2047.
  • 9Zhang W, Liang S, Wu J, et al. Human inhibitory receptor immunoglobulin-like transcript 2 amplifies CD11 b + Gr1+ myeloid- derived suppressor cells that promote long-term survival of allografts. Transplantation, 2008. 86 : 1125-1134.
  • 10李海文,戴夫,彭琼,李颖,吴虓.髓系来源的抑制性细胞免疫学特点及其在自身免疫性疾病中的作用[J].中华微生物学和免疫学杂志,2011,31(7):667-670. 被引量:3

二级参考文献26

  • 1Zhu B, Bando Y, Xiao S, et al. CDllb^+Ly-6C(hi) suppressive monocytes in experimental autoimmune encephalomyelitis. J Im- munol, 2007, 179(8) : 5228-5237.
  • 2Kerr EC, Raveney B J, Copland DA, et al. Analysis of retinal cel- lular infiltrate in experimental autoimmune uveoretinitis reveals multiple regulatory cell populations. J Autoimmun, 2008, 31 (4) : 354-361.
  • 3Haile LA, yon Wasielewski R, Gamrekelashvili J, et al. Myeloid- derived suppressor cells in inflammatory bowel disease: a new im- munoregulatory pathway. Gastroenterology, 2008, 135 ( 3 ) : 871- 881, 881. el-5.
  • 4Highfi11 SL, Rodriguez PC, Zhou Q, et al. Bone marrow myeloid- derived suppressor cells (MDSCs) inhibit graft-versus-host disease (GVHD) via an arginase-1-dependent mechanism that is up-regu- lated by interleukin-13. Blood, 2010, 116 (25) : 5738-5747.
  • 5Gabrilovich DI, Nagaraj S. Myeloid-derived suppressor cells as regulators of the immune system. Nat Rev Immunol, 2009, 9(3) : 162-174.
  • 6Zhang W, Liang S, Wu J, et al. Human inhibitory receptor immu- noglobulin-like transcript 2 amplifies CD1 lb^+Grl^+ myeloid-derived suppressor cells that promote long-term survival of allografts. Transplantation, 2008, 86(8) : 1125-1134.
  • 7Yang R, Cai Z, Zhang Y, et al. CD80 in immune suppression by mouse ovarian carcinoma-associated Gr-1^+CDllb^+ myeloid cells. Cancer Res, 2006, 66(13): 6807-6815.
  • 8Youn JI, Nagaraj S, Collazo M, et al. Subsets of myeloid-derived suppressor ceils in tumor-bearing mice. J Immunol, 2008, 181 ( 8 ) : 5791-5802.
  • 9Ribechini E, Greifenberg V, Sandwick S, et al. Subsets, expan- sion and activation of myeloid-derived suppressor cells. Med Mi- crobiol Immunol, 2010, 199(3): 273-281.
  • 10Sinha P, Clements VK, Ostrand-Rosenberg S. Reduction of mye- loid-derived suppressor ceils and induction of M1 macrophages fa- cilitate the rejection of established metastatic disease. J Immunol, 2005, 174(2) : 636-645.

共引文献2

同被引文献61

  • 1陈万军 ,张烜 .CD_4^+CD_(25)^+T免疫调节细胞在疾病发生和临床应用中的意义[J].中华医学杂志,2005,85(41):2948-2951. 被引量:14
  • 2王聚乐,李长山,顿珠,周惠英.藏药结血蒿水提物的免疫抑制作用研究[J].四川大学学报(医学版),2006,37(6):908-912. 被引量:13
  • 3施国海,周佩军,王祥慧,徐达,施敏敏,陈皓.FTY720对体外混合培养淋巴细胞增殖和凋亡的影响[J].上海交通大学学报(医学版),2007,27(4):380-383. 被引量:6
  • 4Gabrilovich DI, Nagaraj S. Myeloid-derived suppressor cells as regulators of the immune system. Nat Rev Immunol, 2009, 9: 162-174.
  • 5Peranzoni E, Zilio S, Marigo I, et al. Myeloid-derived suppressor cell heterogeneity and subset definition. Carr Opin Immunol, 2010, 22:238-244.
  • 6Movahedi K, Guilliams M, Van den Bossche J, et al. Identification of discrete tumor-induced myeloid-.derived suppressor cell subpopulations with distinct T cell-suppressive activity. Blood, 2008, 111:4233-4244.
  • 7Deshane J, Zmijewski JW, Luther R, et al. Free radical- producing myeloid-derived regulatory cells: potent activators and suppressors of lung inflammation and airway hyperresponsiveness. Mueosal Immunol, 2011,4 : 503-518.
  • 8Saiwai H, Kumamaru H, Ohkawa Y, et al. Ly6C + Ly6G- Myeloid-derived suppressor cells play a critical role in the resolution of acute inflammation and the subsequent tissue repair process after spinal cord injury. J Neurochem, 2013, 125:74-88.
  • 9Dietlin TA, Hofman FM, Lund BT, et al. Mycobacteria-indueed Gr-1 + subsets from distinct myeloid lineages have opposite effectson T cell expansion. J Leukoc Biol, 2007, 81:1205-1212.
  • 10Zhu B, Bando Y, Xiao S, et al. CD11 b ~ Ly-6C (hi) suppressive monocytes in experimental autoimmune encephalomyelitis. J Immunol, 2007, 179:5228-5237.

引证文献3

二级引证文献8

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部