Identification of Suitable Reference Genes for mRNA Studies in Bone Marrow in a Mouse Model of Hematopoietic Stem Cell Transplantation

被引:5
作者
Li, H. [1 ]
Chen, C. [2 ,3 ]
Yao, H. [2 ,3 ]
Li, X. [2 ,3 ]
Yang, N. [2 ,3 ]
Qiao, J. [2 ,3 ,4 ]
Xu, K. [2 ,3 ,4 ]
Zeng, L. [2 ,3 ,4 ]
机构
[1] Xuzhou Med Coll, Affiliated Hosp, Dept Clin Lab, Xuzhou, Peoples R China
[2] Xuzhou Med Coll, Blood Dis Inst, Xuzhou, Peoples R China
[3] Key Lab Bone Marrow Stem Cell, Xuzhou, Jiangsu, Peoples R China
[4] Xuzhou Med Coll, Affiliated Hosp, Dept Hematol, 99 West Huaihai Rd, Xuzhou 221002, Jiangsu, Peoples R China
基金
中国博士后科学基金; 中国国家自然科学基金;
关键词
PROGENITOR CELLS; EXPRESSION; PCR; BETA(2)-MICROGLOBULIN; SELECTION; NICHES; TARGET;
D O I
10.1016/j.transproceed.2016.07.028
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Background. Bone marrow micro-environment changes during hematopoietic stem cell transplantation (HSCT) with subsequent alteration of genes expression. Quantitative polymerase chain reaction (q-PCR) is a reliable and reproducible technique for the analysis of gene expression. To obtain more accurate results, it is essential to find a reference during HSCT. However, which gene is suitable during HSCT remains unclear. This study aimed to identify suitable reference genes for mRNA studies in bone marrow after HSCT. Methods. C57BL/6 mice were treated with either total body irradiation (group T) or busulfan/cyclophosphamide (BU/CY) (group B) followed by infusion of bone marrow cells. Normal mice without treatments were served as a control. All samples (group T + group B + control) were defined as group G. On days 7, 14, and 21 after transplantation, transcription levels of 7 candidate genes, ACTB, B2M, GAPDH, HMBS, HPRT, SDHA, and YWHAZ, in bone marrow cells were measured by use of real-time quantitative PCR. The expression stability of these 7 candidate reference genes were analyzed by 2 statistical software programs, GeNorm and NormFinder. Results. Our results showed that ACTB displayed the highest expression in group G, with lowest expression of PSDHA in group T and HPRT in groups B and G. Analysis of expression stability by use of GeNorm or NormFinder demonstrated that expression of B2M in bone marrow were much more stable during HSCT, compared with other candidate genes including commonly used reference genes GAPDH and ACTB. Conclusions. ACTB could be used as a suitable reference gene for mRNA studies in bone marrow after HSCT.
引用
收藏
页码:2826 / 2832
页数:7
相关论文
共 31 条
  • [1] Busulphan-Cyclophosphamide Cause Endothelial Injury, Remodeling of Resistance Arteries and Enhanced Expression of Endothelial Nitric Oxide Synthase
    Al-Hashmi, Sulaiman
    Boels, Piet J. M.
    Zadjali, Fahad
    Sadeghi, Behnam
    Sallstrom, Johan
    Hultenby, Kjell
    Hassan, Zuzana
    Arner, Anders
    Hassan, Moustapha
    [J]. PLOS ONE, 2012, 7 (01):
  • [2] Al-Hashmi S, 2011, INT J CLIN EXP PATHO, V4, P596
  • [3] Normalization of real-time quantitative reverse transcription-PCR data: A model-based variance estimation approach to identify genes suited for normalization, applied to bladder and colon cancer data sets
    Andersen, CL
    Jensen, JL
    Orntoft, TF
    [J]. CANCER RESEARCH, 2004, 64 (15) : 5245 - 5250
  • [4] Osteoblastic cells regulate the haematopoietic stem cell niche
    Calvi, LM
    Adams, GB
    Weibrecht, KW
    Weber, JM
    Olson, DP
    Knight, MC
    Martin, RP
    Schipani, E
    Divieti, P
    Bringhurst, FR
    Milner, LA
    Kronenberg, HM
    Scadden, DT
    [J]. NATURE, 2003, 425 (6960) : 841 - 846
  • [5] Association between serum β2-microglobulin level and infectious mortality in hemodialysis patients
    Cheung, Alfred K.
    Greene, Tom
    Leypoldt, John K.
    Yan, Guofen
    Allon, Michael
    Delmez, James
    Levey, Andrew S.
    Levin, Nathan W.
    Rocco, Michael V.
    Schulman, Gerald
    Eknoyan, Garabed
    [J]. CLINICAL JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY, 2008, 3 (01): : 69 - 77
  • [6] SLAM family receptors distinguish hematopoietic stem and progenitor cells and reveal endothelial niches for stem cells
    Kiel, MJ
    Yilmaz, ÖH
    Iwashita, T
    Yilmaz, OH
    Terhorst, C
    Morrison, SJ
    [J]. CELL, 2005, 121 (07) : 1109 - 1121
  • [7] Reference genes for real-time qPCR in leukocytes from asthmatic patients before and after anti-asthma treatment
    Kozmus, Carina E. P.
    Potocnik, Uros
    [J]. GENE, 2015, 570 (01) : 71 - 77
  • [8] Reference genes in the developing murine brain and in differentiating embryonic stem cells
    Kraemer, Nadine
    Neubert, Gerda
    Issa, Lina
    Ninnemann, Olaf
    Seiler, Andrea E. M.
    Kaindl, Angela M.
    [J]. NEUROLOGICAL RESEARCH, 2012, 34 (07) : 664 - 668
  • [9] Reference genes for gene expression analysis in proliferating and differentiating human keratinocytes
    Lanzafame, Manuela
    Botta, Elena
    Teson, Massimo
    Fortugno, Paola
    Zambruno, Giovanna
    Stefanini, Miria
    Orioli, Donata
    [J]. EXPERIMENTAL DERMATOLOGY, 2015, 24 (04) : 314 - 316
  • [10] Lee WJ, 2015, REPROD FERTIL DEV