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长期液氮保存PBSC细胞凋亡及死亡检测

Detect to Necrosis and Apoptosis of PBSC for Long-term Cryopreserred by Liquefaction of Nitrogen
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摘要 目的比较外周血干细胞(Peripheral blood stem cell,PBSC)采集物中有核细胞经长期深低温保存后细胞凋亡及死亡率与新鲜采集物的差异,便于对PBSC进行活力评价。方法47份外周血干细胞采集物标本,新鲜对照标本12份,实验I组为液氮保存2~4年的PBSC26份,实验II组为液氮保存5~7年的PBSC9份,以流式细胞仪检测各组有核细胞中核酸染料7AAD着色的细胞百分比(代表死亡率),以及有核细胞中表达活化的caspase-3的细胞百分比(代表凋亡率)。结果两实验组的细胞死亡率和凋亡率均高于对照组(P<0.05),实验II组凋亡率为35.6%±17.51%,与实验I组(24.14%±16.87%)的差异有显著性(P=0.031)。结论深低温保存2~7年的PBSC采集物中有核细胞活性较新鲜PBSC采集物低,凋亡率及死亡率升高。 Objective To compare nucleated cell viability between the fresh and the long-term cryopreserved PBSC collections,to assist the judgment on the activity of PBSC. Methods Among the total 47 samples of PBSC collections, frozen samples were divided into two groups: group 1(cryopreserred for 2-4 years,n=26) and group 2 (cryopreservd for 5-7 years,n=9) ;fresh samples (n=12) were taken as control. Flow cytometry method (FCM) based on 7AAD or caspase-3 staining was applied to assess the degree of cell necrosis (7AAD+) or apoptosis(caspase-3+) in cryopreserved and red-cell lytic collection samples. Results Both the necrosis and apoptosis levels of group 1 and group 2 were higher than those of control group(P〈0.05); apoptosis cell of group 2 was more than that of group 1 (35.6%±17.51% to 24.14± 16. 87% ,P = 0. 031). Conclusion Compared with the fresh PBSC collections, the long-term frozend ones had decreased NCs viabilities.
出处 《临床输血与检验》 CAS 2008年第1期40-42,共3页 Journal of Clinical Transfusion and Laboratory Medicine
关键词 外周血干细胞 流式细胞术 造血干细胞 Peripheral blood stem cell Flow cytometry Hematopoietic stem cell
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  • 1Zhao-You Tang Liver Cancer Institute & Zhongshan Hospital of Fudan University Professor of Surgery Chairman.Liver Cancer Institute of Fudan University(previous Liver Cancer Institute of Shanghai Medical University)136 Yixueyuan Road,Zhongshan Hospital,Shanghai 200032,China..Hepatocellular Carcinoma-Cause,Treatment and Metastasis[J].World Journal of Gastroenterology,2001,7(4):445-454. 被引量:214
  • 2[1]de Boer F, Drager AM, Pinedo HM, et al. Early apoptosis largely accounts for functional impairment of CD34 + cells in frozen-thawed stem cell grafts. J Hematother Stem Cell Res, 2002; 11: 951-963 被引量:1
  • 3[2]Schuurhuis GJ, Muijen MM, Oberink JW, et al. Large populations of non-clonogenic early apoptotic CD34-positive cells are present in frozen-thawed peripheral blood stem cell transplants. BBone Marrow Transplant, 2001; 27: 487 - 498 被引量:1
  • 4[3]Baust JM, Vogel MJ, Van Buskirk R, et al. A molecular basis of cryopreservation failure and its modulation to improve cell survival.Cell Transplant, 2001; 10:561-571 被引量:1
  • 5[4]Stroh C, Cassens U, Samraj AK, et al. The role of caspases in cryoinjury: caspase inhibition strongly improves the recovery of cryopreserved hematopoietic and other cells. FASEB J, 2002; 16: 1651- 1653 被引量:1
  • 6[5]Peter AT, Linde-Forsberg C. Efficacy of the anticaspase agent zVAD-fmk on post-thaw viability of canine spermtozoa. Theriogenology, 2003; 59:1525 - 1532 被引量:1
  • 7[6]Eroglu A, Russo M J , Bieganski R, et al. Intracellular trehalose improves the survival of cryopreserved mammalian cells. Nat Biotechnol, 2000; 18: 163-167 被引量:1
  • 8[7]Limaye L S, Kale V P. Cryopreservation of human hematopoietic cells with membrane stabilizers and bioantioxidants as additives in the conventional freezing mediuin. J Hematother Stem Cell Res, 2001;10:709-718 被引量:1
  • 9[8]Rauen U, Polzar B, Stephan H, et al. Cold-induced apoptosis in cultured hepatocytes and liver endothelial cells: mediation by reactive oxygen species. FASEBJ, 1999; 13:155-168 被引量:1
  • 10[9]Schulze-Osthoff K, Ferrari D, Los M, et al. Apoptosis signaling by death receptors. Eur J Biochem, 1998; 254:439-459 被引量:1

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