Bone Marrow Mononuclear Cell Transplantation Improves Survival and Induces Hepatocyte Proliferation in Rats after CCl4 Acute Liver Damage

被引:8
|
作者
Baldo, Guilherme [1 ,2 ]
Giugliani, Roberto [1 ,2 ,3 ]
Uribe, Carolina [1 ]
Belardinelli, Maria Cristina [1 ,2 ]
Soares Duarte, Marcos Eugenio [4 ]
Meurer, Luise [5 ]
da Silveira, Themis Reverbel [6 ]
Matte, Ursula [1 ,6 ]
机构
[1] Hosp Clin Porto Alegre, Res Ctr, Gene Therapy Ctr, Porto Alegre, RS, Brazil
[2] Univ Fed Rio Grande do Sul, Postgrad Program Biochem, Porto Alegre, RS, Brazil
[3] Hosp Clin Porto Alegre, Med Genet Serv, Porto Alegre, RS, Brazil
[4] Hosp Clin Porto Alegre, Expt Anim Unit, Res Ctr, Porto Alegre, RS, Brazil
[5] Hosp Clin Porto Alegre, Pathol Serv, Porto Alegre, RS, Brazil
[6] Hosp Clin Porto Alegre, Res Ctr, Expt Hepatol Lab, Porto Alegre, RS, Brazil
关键词
Acute liver failure; Bone marrow stem cells; Carbon tetrachloride; Cell therapy; Conditioned medium; Hepatocyte proliferation; HEMATOPOIETIC STEM-CELLS; CARBON-TETRACHLORIDE; INJURY; EXPRESSION; INFUSION; DIFFERENTIATION; FIBROBLASTS; THERAPY; MODEL;
D O I
10.1007/s10620-010-1195-4
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
The aim of this research was to evaluate the effects of bone marrow mononuclear cell (BMC) transplantation in rats with toxic acute liver damage induced by carbon tetrachloride (CCl4). Cells from male Wistar rats were obtained using Ficoll density gradient and 0.2 ml (1 x 10(6) cells) were injected into the portal vein of female rats (n = 15) 24 h after damage. Sham group (n = 15) was performed injecting only vehicle in CCl4-treated animals. Survival, liver histology, number of mitosis and apoptosis, and identification of stained donor cells were observed 72 h after damage. ALT levels were measured at 0 h, 24 h, 48 h, and 72 h after injury. Donor cells could be detected in recipient rats' livers by fluorescence staining and Sry PCR. The treated group revealed a significant improvement in survival rate after 72 h (p = 0.003). There was also a significant increase in the number of mitotic events in treated livers (p = 0.029). This result was confirmed using an in vitro cell proliferation assay in isolated hepatocytes treated with conditioned medium from BMC. ALT was reduced in the treated group after 72 h (p = 0.034). Results indicate that BMC transplantation has potential as a new therapeutic option for acute liver disease and suggest that these cells may contribute to hepatic recovery through release of mitotic cytokines.
引用
收藏
页码:3384 / 3392
页数:9
相关论文
共 50 条
  • [41] DOSE-DEPENDENT CONTRIBUTION OF HUMAN PERIPHERAL BLOOD CD34-POSITIVE CELL TRANSPLANTATION TO HEPATIC REGENERATION AFTER CCL4 CHRONIC LIVER INJURY
    Nakamura, Toru
    Tsutsumi, Victor
    Torimura, Takuji
    Naitou, Masako
    Iwamoto, Hideki
    Hashimoto, Osamu
    Taniguchi, Eitaro
    Ueno, Takato
    Sata, Michio
    HEPATOLOGY, 2010, 52 (04) : 1271A - 1271A
  • [42] Transplantation of Roxadustat-preconditioned bone marrow stromal cells improves neurological function recovery through enhancing grafted cell survival in ischemic stroke rats
    Chen, Jiayu
    Lin, Xiao
    Yao, Chaojie
    Bingwa, Lebohang Anesu
    Wang, Hao
    Lin, Zhongxiao
    Jin, Kunlin
    Zhuge, Qichuan
    Yang, Su
    CNS NEUROSCIENCE & THERAPEUTICS, 2022, 28 (10) : 1519 - 1531
  • [43] Bone Marrow Mononuclear Cell Transplantation Increases Metalloproteinase-9 and 13 and Decreases Tissue Inhibitors of Metalloproteinase-1 and 2 Expression in the Liver of Cholestatic Rats
    de Carvalho, Simone Nunes
    Helal-Neto, Edward
    de Andrade, Daniela Caldas
    Costa Cortez, Erika Afonso
    Thole, Alessandra Alves
    Barja-Fidalgo, Christina
    de Carvalho, Lais
    CELLS TISSUES ORGANS, 2013, 198 (02) : 139 - 148
  • [44] Autologous bone marrow-derived mesenchymal stem cell transplantation promotes liver regeneration after portal vein embolization in cirrhotic rats
    Li, Tingjun
    Zhu, Jin
    Ma, Kuansheng
    Liu, Nianzhou
    Feng, Kai
    Li, Xiaowu
    Wang, Shuguang
    Bie, Ping
    JOURNAL OF SURGICAL RESEARCH, 2013, 184 (02) : 1161 - 1173
  • [45] Preconditioning of bone marrow mesenchymal stem cells by prolyl hydroxylase inhibition enhances cell survival and angiogenesis in vitro and after transplantation into the ischemic heart of rats
    Xian-Bao Liu
    Jian-An Wang
    Xiao-Ya Ji
    Shan Ping Yu
    Ling Wei
    Stem Cell Research & Therapy, 5
  • [46] Preconditioning of bone marrow mesenchymal stem cells by prolyl hydroxylase inhibition enhances cell survival and angiogenesis in vitro and after transplantation into the ischemic heart of rats
    Liu, Xian-Bao
    Wang, Jian-An
    Ji, Xiao-Ya
    Yu, Shan Ping
    Wei, Ling
    STEM CELL RESEARCH & THERAPY, 2014, 5
  • [47] Decreased collagen types I and IV, laminin, CK-19 and α-SMA expression after bone marrow cell transplantation in rats with liver fibrosis
    S. N. Carvalho
    D. C. Lira
    G. P. Oliveira
    A. A. Thole
    A. C. Stumbo
    C. E. Caetano
    R. G. Marques
    L. Carvalho
    Histochemistry and Cell Biology, 2010, 134 : 493 - 502
  • [48] Decreased collagen types I and IV, laminin, CK-19 and α-SMA expression after bone marrow cell transplantation in rats with liver fibrosis
    Carvalho, S. N.
    Lira, D. C.
    Oliveira, G. P.
    Thole, A. A.
    Stumbo, A. C.
    Caetano, C. E.
    Marques, R. G.
    Carvalho, L.
    HISTOCHEMISTRY AND CELL BIOLOGY, 2010, 134 (05) : 493 - 502
  • [49] Comparison of the Treatment Efficiency of Bone Marrow-Derived Mesenchymal Stem Cell Transplantation via Tail and Portal Veins in CCl4-Induced Mouse Liver Fibrosis
    Nhung Hai Truong
    Nam Hai Nguyen
    Trinh Van Le
    Ngoc Bich Vu
    Nghia Huynh
    Thanh Van Nguyen
    Huy Minh Le
    Ngoc Kim Phan
    Phuc Van Pham
    STEM CELLS INTERNATIONAL, 2016, 2016
  • [50] Conditioned Medium from Bone Marrow-Derived Mesenchymal Stem Cells Improves Recovery after Spinal Cord Injury in Rats: An Original Strategy to Avoid Cell Transplantation
    Cantinieaux, Dorothee
    Quertainmont, Renaud
    Blacher, Silvia
    Rossi, Loic
    Wanet, Thomas
    Noel, Agnes
    Brook, Gary
    Schoenen, Jean
    Franzen, Rachelle
    PLOS ONE, 2013, 8 (08):