Abstract:【Objective】To establish a simple and efficient in vitro isolation and culture system for bone marrow-derived precursor cells (DC) in rats.【Methods】 Granulocyte macrophage colony stimulating factor (GM-CSF) and interleukin -4 (IL-4) were used to induce and separate rat bone marrow hematopoietic progenitor cells to get immature dendritic cells after 7 d (imDC), immunomagnetic flow cytometry was used before and after purification of the surface of imDC to test positive expression rate of OX62. Lipopolysaccharide (LPS) lasted for 2 D to stimulate imDC maturation to get mature dendritic cells (mature dendritic cell, mDC), flow cytometry was used to detect imDC and mDC cell surface CD86, CD80, RT1B positive expression rate ; ELISA was used to detect the secretion of IL-12 in vitro in two groups of cells, mixed lymphocyte reaction (MLR) was used to determine lymphocyte proliferation ability of cells in two groups.【Results】Purified imDC surface OX62 positive expression rate was 91.9%, significantly higher than that before purification 82.8% (P<0.05); imDC, CD80, CD86 on the surface of the positive expression rates of RT1B were 11.48%, 6.25%, 77.2%, stimulated by LPS after the maturity of the mDC surface CD86, CD80 and RT1B positive expression rates were 91.38%, 93.54%, 98.6% imDC; cell IL-12 secretion level (36±9) pg/mL, was significantly lower than that of mDC (228 ±27) pg/mL (P<0.01) MLR results in mDC group; ability to stimulate T lymphocyte proliferation was significantly higher than that of the imDC group.【Conclusion】In this experiment, the cultured cells were identified by three aspects (cell morphology observation, surface molecular markers and functional status), and it was proved that the combination of GM-CSF+IL-4 could induce high purity and large numbers of DC in vitro; through the purification of immunomagnetic beads, a relatively large number of DC with high purity can be obtained to meet the experimental requirements.
黄江波,罗志刚,刘宇明,刘利,何群君,言彩红,李建军,龙向阳. 大鼠骨髓来源树突状细胞的体外分离培养鉴定初步研究[J]. 医学临床研究, 2018, 35(1): 4-7.
Huang Jiang-bo,LUO Zhi-gang,LIU Yu-ming,et al. A Simple and Efficient In Vitro Isolation and Culture System for Bone Marrow-Derived Precursor Cells (DC) in Rats. JOURNAL OF CLINICAL RESEARCH, 2018, 35(1): 4-7.
[1] Solari MG,Thomson AW.Human dendritic cells and transplant outcome[J].Transplantation,2008,85(11):1513-1522. [2] Hart DN.Dendritic cells: unique leukocyte populations which control the primary immune response[J].Blood,1997,90(9):3245-3287. [3] Mineharu Y ,King GD ,Muhammad AK,et al.Engineering the brain tumor microenvironment enhances the efficacy of dendritic cell vaccination: implications for clinical trial design[J].Clin Cancer Res,2011,17 (14):4705-4718. [4] 张升宁,李立,冉江华,等.大鼠骨髓来源树突状细胞的分离、培养及鉴定[J].昆明医学院学报,2008,29(2);41-44. [5] 方航荣,陈丽红,邱明链,等.大鼠骨髓来源树突状细胞的体外培养与鉴定[J].山西医科大学学报,2010,41(8);740-744. [6] Son YI,Egawa S,Tatsumi T,et al.A novel bulk-culture method for generating mature dendritic cells from mouse bone marrow cells[J].J Immunol Methods,2002 ,262(1-2): 145-157. [7] Brenan M,Puklavec M.The MRC OX-62 antigen:a useful marker in the Purification of rat veiled cells with the biochemical properties of an integrin [J].J Exp Med,1992,175(6) :1457-1465. [8] De Jong EC,Vieira PL,Kalinski P,et al.Microbial selectively Thl cell-Promoting or Th2-Promoting dendritic cells in vitro with diverse Th cell-polarizing signals[J].J Immunol,2002,168(4):1704-1709. [9] Kuipers H,Heirman C,Hijdra D,et al.Dendritic cells retrovirally overexpressing IL-12 induce strong Th1 responses to inhaled antigen in the lung but fail to revert established Th2 sensitization [J].Leukoc Biol,2004,76(5):1028-1038. [10] Turnquist HR,Fischer RT,Thomson AW.Pharmacological modification of dendritic cells to promote their tolerogenicity in transplantation[J].Methods Mol Biol,2010,595:135-148.