期刊文献+

5-氟尿嘧啶诱导的造血损伤中骨髓基质重建相关基因的表达及其意义

Expression Changes of Matrix Reconstitution-related Genes in Bone Marrow during 5-Fluorouracil-Induced Hemopoietic Injury and Their Significance
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摘要 目的:探究胞外基质重建相关基因在氟尿嘧啶(5-fluorouracil,5-FU)诱导的造血损伤重建中的表达及其意义。方法:采用C57BL/6小鼠腹腔注射5-FU(200 mg/kg)建立造血损伤模型。注射后3、6、9、15、21、27 d常规检测外周血象;在相同时间点用TRIzol法提取骨髓总RNA,反转录后以实时荧光定量PCR(RT-q PCR)检测胞外基质重建相关基因的mRNA水平,包括细胞外基质(ECM-1)、明胶酶(MMP-2)、基质降解素(MMP-3)、胶原酶(MMP-13)、组织金属酶抑制剂(TIMP-1)基因。结果:小鼠经5-FU注射后外周血出现典型的造血损伤与修复过程,且红细胞、白细胞、血小板损伤修复的动态不同;RT-q PCR显示在5-FU损伤期骨髓胞外基质重建相关基因的表达均显著上调,MMP-2在注射5-FU后第3天时表达最高,MMP-3、MMP-13、TIMP-1、ECM-1在第6天表达最高;MMP-3在骨髓中表达较低,但损伤后上升幅度最大。结论:在5-FU建立的骨髓造血损伤模型中,胞外基质重建相关基因可能参与造血损伤和随后骨髓基质的重构过程,且不同基因发挥的时段和作用对象不同,但彼此协同为造血损坏后重建奠定基础。 Objective: To explore the expression change of the genes related with matrix reconstitution during the injury and reconstitution of murine bone marrow following treatment with 5-fluorouracil (5-FU). Methods:C57BL/6 mice received intraperitoneal injection of 5-FU (200 mg/kg), and peripheral blood cell counts were monitored at 3, 6, 9, 15, 21, 27 days after treatment. Bone marrow cells were harvested at these times for total RNA extraction using TRIzol. Reverse transcriptions in combination with real-time PCR were performed for detecting expression of genes related with matrix reconstitution, including ECM-1, MMP-2, MMP-3, MMP-13 and TIMP-1. Results: After injection of 5-FU, the numbers of three line cells in peripheral blood (i. e. RBC, WBC and platelets ) decreased and then recovered with differential dynamics. Similarly, RT-qPCR revealed that all the 5 detected gene expressions were significantly up-regulated during the injury. The mRNA expression of MMP-2 reached to peak at day 3 while the other genes reached to peak at day 6. MMP-3 has a low expression when compared with others, but its expression increased significantly after injury. Conclusion: In 5-FU induced hematopoietic injury and reconstitution model, matrix reconstitution-related genes may play an important role in hematopoietic reconstitution, but different genes play different roles at various time, and cooperate with each other for hematopoietic reconstitution.
出处 《中国实验血液学杂志》 CAS CSCD 北大核心 2015年第3期848-851,共4页 Journal of Experimental Hematology
关键词 5-氟尿嘧啶 造血损伤 细胞外基质 MMP TIMP-1 5-fluorouracil hematopoietic damage extraceUular matrix MMP TIMP-1
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参考文献11

  • 1Votteler M,Kluger PJ,Walles H,et al.Stem cell microenvironments—unveiling the secret of how stem cell fate is defined.Macromol Biosci,2010;10(11):1302-1315.
  • 2Longley DB,Harkin DP,Johnston PG.5-fluorouracil:mechanisms of action and clinical strategies.Nat Rev Cancer,2003;3(5):330-338.
  • 3Hwang HS,Davis TW,Houghton JA,et al.Radiosensitivity of thymidylate synthase-deficient human tumor cells is affected by progression through the G1 restriction point into S-phase:implications for fluoropyrimidine radiosensitization.Cancer Res,2000;60(1):92-100.
  • 4De Angelis PM,Svendsrud DH,Kravik KL,et al.Cellular response to 5-fluorouracil(5-FU)in 5-FU-resistant colon cancer cell lines during treatment and recovery.Mol Cancer,2006;5:20.
  • 5刘智敏.基质金属蛋白酶的结构、功能和调节[J].生物医学工程学杂志,2002,19(4):680-683. 被引量:31
  • 6Heissig B,Hattori K,Dias S,et al.Recruitment of stem and progenitor cells from the bone marrow niche requires MMP-9 mediated release of kit-ligand.Cell,2002;109(5):625-637.
  • 7Wrzyszcz A,Wozniak M.On the origin of matrix metalloproteinase-2and-9 in blood platelets.Platelets,2012;23(6):467-474.
  • 8Nakamura-Ishizu A,Okuno Y,Omatsu Y,et al.Extracellular matrix protein tenascin-C is required in the bone marrow microenvironment primed for hematopoietic regeneration.Blood,2012;119(23):5429-5437.
  • 9Malara A,Gruppi C,Rebuzzini P,et al.Megakaryocyte-matrix interaction within bone marrow:new roles for fibronectin and factor XIIIA.Blood,2011;117(8):2476-2483.
  • 10Yu XF,Han ZC.Matrix metalloproteinases in bone marrow:roles of gelatinases in physiological hematopoiesis and hematopoietic malignancies.Histol Histopathol,2006;21(5):519-531.

二级参考文献25

  • 1Rooney PH, Murray GI, Stevenson DAJ, et al. Comparative genomic hybridization and chromosomal instability in solid tumouts. Br J Cancer,1999;80 : 862
  • 2Kleiner D, Stetler-Stevenson W. Matrix metalloproteinases and metastasis. Cancer Chemother Phamacol, 1999 ; 43(suppl) : 42
  • 3Hozumi A, Nishimura Y, Nishiuma T, et al. Induction of MMP-9 in normal human bronchial epithelial cells by TNF-alpha via NF-kappa B-mediated pathway. Am J Physiol Lung Cell Mol Physiol, 2001; 281(6) : 1444
  • 4Mengshol JA, Vincenti MP, Brinckerhoff CE, et al. IL-1 induces collagenase-3 (MMP-13) promoter activity in stably transfected chondrocytic cells: requirement for Runx-2 and activation by p38 MAPK and JNK pathways. Nucleic Acids Res.2001; 29(21) : 4361
  • 5Alper O, Bergmann-Leitner ES, Bennett TA, et al. Epidermal growth factor receptor signaling and the invasive phenotype of ovarian carcinoma cells. J Natl Cancer Inst, 2001; 93(18) : 1375
  • 6Alexander JP, Acott TS. Involvement of protein kinase C in TNFalpha regulation of trabecular matrix metalloproteinases and TIMPs. Invest Ophthalmol Vis Sci, 2001; 42(12) : 2831
  • 7Yang JQ, Zhao W, Duan H, et al. v-Ha-RaS oncogene upregulates the 92-kDa type Ⅳ collagenase (MMP-9) gene by increasing cellular superoxide production and activating NF-kappaB.Free Radic Biol Med, 2001; 31(4) : 520
  • 8Yoon A, Hurta RA. Insulin like growth factor-1 selectively regulates the expression of matrix metalloproteinase-2 in malignant H-ras transformed cells. Mol Cell Biochem, 2001; 223(1-2) : 1
  • 9Wick W, Plattern M, Weller M, et al. Glioma cell invasion:regulation of metalloproteinase activity by TGF-beta. J Neurooncol, 2001; 53(2) : 177
  • 10Frankenberger M, Hauck RW, Frankenberger B, et al. All trans-retinoic acid selectively down-regulates matrix metalloproteinase-9 (MMP-9) and up-regulates tissue inhibitor of metalloproteinase-1 (TIMP-1) in human bronchoalveolar lavage cells. Mol Med, 2001; 7(4) : 263

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