Bone marrow mononuclear cell therapy in experimental allergic asthma: Intratracheal versus intravenous administration

被引:29
作者
Abreu, Soraia C. [1 ]
Antunes, Mariana A. [1 ]
Maron-Gutierrez, Tatiana [1 ,2 ]
Cruz, Fernanda F. [1 ]
Ornellas, Debora S. [1 ,2 ]
Silva, Adriana L. [1 ]
Diaz, Bruno L. [3 ]
Ab'Saber, Alexandre M. [4 ]
Capelozzi, Vera L. [4 ]
Xisto, Debora G. [1 ,2 ]
Morales, Marcelo M. [2 ]
Rocco, Patricia R. M. [1 ]
机构
[1] Univ Fed Rio de Janeiro, Carlos Chagas Filho Inst Biophys, Lab Pulm Invest, BR-21941902 Rio De Janeiro, RJ, Brazil
[2] Univ Fed Rio de Janeiro, Carlos Chagas Filho Inst Biophys, Lab Cellular & Mol Physiol, BR-21941902 Rio De Janeiro, RJ, Brazil
[3] Univ Fed Rio de Janeiro, Carlos Chagas Filho Inst Biophys, Lab Inflammat, BR-21941902 Rio De Janeiro, RJ, Brazil
[4] Univ Sao Paulo, Sch Med, Dept Pathol, Sao Paulo, Brazil
基金
巴西圣保罗研究基金会;
关键词
Collagen; Lung mechanics; Stem cells; Asthma; Growth factor; MESENCHYMAL STEM-CELLS; MURINE MODEL; LUNG-MECHANICS; AIRWAY; INFLAMMATION; BRONCHOSCOPY; EXPRESSION; CONTRIBUTE; BLEOMYCIN; PULMONARY;
D O I
10.1016/j.resp.2012.11.005
中图分类号
Q4 [生理学];
学科分类号
071003 ;
摘要
We hypothesized that the route of administration would impact the beneficial effects of bone marrow-derived mononuclear cell (BMDMC) therapy on the remodelling process of asthma. C57BL/6 mice were randomly assigned to two main groups. In the OVA group, mice were sensitized and challenged with ovalbumin, while the control group received saline using the same protocol. Twenty-four hours before the first challenge, control and OVA animals were further randomized into three subgroups to receive saline (SAL), BMDMCs intravenously (2 x 10(6)), or BMDMCs intratracheally (2 x 10(6)). The following changes were induced by BMDMC therapy in OVA mice regardless of administration route: reduction in resistive and viscoelastic pressures, static elastance, eosinophil infiltration, collagen fibre content in airways and lung parenchyma; and reduction in the levels of interleukin (IL)-4, IL-13, transforming growth factor-beta and vascular endothelial growth factor. In conclusion, BMDMC modulated inflammatory and remodelling processes regardless of administration route in this experimental model of allergic asthma. (C) 2012 Elsevier B.V. All rights reserved.
引用
收藏
页码:615 / 624
页数:10
相关论文
共 43 条
  • [1] Cells derived from the circulation contribute to the repair of lung injury
    Abe, S
    Boyer, C
    Liu, XD
    Wen, FQ
    Kobayashi, T
    Fang, QH
    Wang, XQ
    Hashimoto, M
    Sharp, JG
    Rennard, SI
    [J]. AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE, 2004, 170 (11) : 1158 - 1163
  • [2] Mechanisms of cellular therapy in respiratory diseases
    Abreu, Soraia C.
    Antunes, Mariana A.
    Pelosi, Paolo
    Morales, Marcelo M.
    Rocco, Patricia R. M.
    [J]. INTENSIVE CARE MEDICINE, 2011, 37 (09) : 1421 - 1431
  • [3] Effects of bone marrow-derived mononuclear cells on airway and lung parenchyma remodeling in a murine model of chronic allergic inflammation
    Abreu, Soraia C.
    Antunes, Mariana A.
    Maron-Gutierrez, Tatiana
    Cruz, Fernanda F.
    Carmo, Luana G. R. R.
    Ornellas, Debora S.
    Carreira Junior, Humberto
    AbiSaber, Alexandre M.
    Parra, Edwin R.
    Capelozzi, Vera L.
    Morales, Marcelo M.
    Rocco, Patricia R. M.
    [J]. RESPIRATORY PHYSIOLOGY & NEUROBIOLOGY, 2011, 175 (01) : 153 - 163
  • [4] Epithelial to mesenchymal transition (EMT) induced by bleomycin or TFGb1/EGF in murine induced pluripotent stem cell-derived alveolar Type II-like cells
    Alipio, Zaida A.
    Jones, Nathan
    Liao, Wenbin
    Yang, Jianchang
    Kulkarni, Shilpa
    Kumar, K. Sree
    Hauer-Jensen, Martin
    Ward, David C.
    Ma, Yupo
    Fink, Louis M.
    [J]. DIFFERENTIATION, 2011, 82 (02) : 89 - 98
  • [5] Analysis of NLRP3 in the Development of Allergic Airway Disease in Mice
    Allen, Irving C.
    Jania, Corey M.
    Wilson, Justin E.
    Tekeppe, Erin M.
    Hua, Xiaoyang
    Brickey, Willie J.
    Kwan, Mildred
    Koller, Beverly H.
    Tilley, Stephen L.
    Ting, Jenny P. -Y.
    [J]. JOURNAL OF IMMUNOLOGY, 2012, 188 (06) : 2884 - 2893
  • [6] Sex-specific lung remodeling and inflammation changes in experimental allergic asthma
    Antunes, Mariana A.
    Abreu, Soraia C.
    Silva, Adriana L.
    Parra-Cuentas, Edwin R.
    Ab'Saber, Alexandre M.
    Capelozzi, Vera L.
    Ferreira, Tatiana P. T.
    Martins, Marco A.
    Silva, Patricia M. R.
    Rocco, Patricia R. M.
    [J]. JOURNAL OF APPLIED PHYSIOLOGY, 2010, 109 (03) : 855 - 863
  • [7] Different strains of mice present distinct lung tissue mechanics and extracellular matrix composition in a model of chronic allergic asthma
    Antunes, Mariana A.
    Abreu, Soraia C.
    Damaceno-Rodrigues, Nilsa R.
    Parra, Edwin R.
    Capelozzi, Vera L.
    Pinart, Mariona
    Romero, Pablo V.
    Silva, Patricia M. R.
    Martins, Marco Aurelio
    Rocco, Patricia R. M.
    [J]. RESPIRATORY PHYSIOLOGY & NEUROBIOLOGY, 2009, 165 (2-3) : 202 - 207
  • [8] Bone marrow-derived mononuclear cell therapy in experimental pulmonary and extrapulmonary acute lung injury
    Araujo, Indianara M.
    Abreu, Soraia C.
    Maron-Gutierrez, Tatiana
    Cruz, Fernanda
    Fujisaki, Livia
    Carreira, Humberto, Jr.
    Ornellas, Felipe
    Ornellas, Debora
    Vieira-de-Abreu, Adriana
    Castro-Faria-Neto, Hugo C.
    Ab'Saber, Alexandre Muxfeldt
    Teodoro, Walcy R.
    Diaz, Bruno L.
    DaCosta, Carlos Peres
    Capelozzi, Vera L.
    Pelosi, Paolo
    Morales, Marcelo M.
    Rocco, Patricia R. M.
    [J]. CRITICAL CARE MEDICINE, 2010, 38 (08) : 1733 - 1741
  • [9] Innate IL-13-producing nuocytes arise during allergic lung inflammation and contribute to airways hyperreactivity
    Barlow, Jillian L.
    Bellosi, Agustin
    Hardman, Clare S.
    Drynan, Lesley F.
    Wong, See Heng
    Cruickshank, James P.
    McKenzie, Andrew N. J.
    [J]. JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY, 2012, 129 (01) : 191 - U275
  • [10] INTERRUPTER RESISTANCE ELUCIDATED BY ALVEOLAR PRESSURE MEASUREMENT IN OPEN-CHEST NORMAL DOGS
    BATES, JHT
    LUDWIG, MS
    SLY, PD
    BROWN, K
    MARTIN, JG
    FREDBERG, JJ
    [J]. JOURNAL OF APPLIED PHYSIOLOGY, 1988, 65 (01) : 408 - 414