To test this hypothesis, lung histology findings, collagen fibre content in the airway and alveolar septa, levels of cytokines and growth factors in lung tissue, and lung mechanics were analyzed following IT and IV administration of BMDMCs in a Olaparib murine model of allergic asthma. This study was approved by the Ethics Committee of the Health Sciences Centre, Federal University of Rio de Janeiro. All animals received humane care in compliance with the “Principles of Laboratory Animal Care” formulated by the National Society for Medical Research and the U.S. National

Research Council “Guide for the Care and Use of Laboratory Animals”. Bone marrow cells were extracted from

male C57BL/6 mice (weight 20–25 g, n = 10) and administered on the day of collection. Alternatively, BMDMCs were obtained from GFP+ male mice (weight 20–25 g, n = 5) and administered to RO4929097 concentration C57BL/6 female mice to evaluate the degree of pulmonary GFP+ cell engraftment. Briefly, bone marrow cells were aspirated from the femur and tibia by flushing the bone marrow cavity with Dulbecco’s modified Eagle’s medium (DMEM) (Life Technologies, Grand Island, NY, USA). After a homogeneous cell suspension was achieved, cells were centrifuged (400 × g for 10 min), re-suspended in DMEM and added to Ficoll-Hypaque (Histopaque 1083, Sigma Chemical Co., St. Louis, MO, USA), and again centrifuged and re-suspended in phosphate-buffered saline (PBS). Cells were counted in a Neubauer Reverse transcriptase chamber with Trypan Blue for the evaluation of viability. For the administration of saline or BMDMCs, mice were anaesthetized with sevoflurane, the jugular vein or the trachea of each mouse was dissected, and cells were slowly injected. A small aliquot of mononuclear cells was used for immunophenotypic characterization of the injected cell population. Cell characterization was performed by flow cytometry using antibodies against CD45 (leukocytes), CD34 (haematopoietic

precursors), CD3, CD8, and CD4 (T lymphocytes), CD19 (B lymphocytes), CD14 (monocytes), CD11b, CD29 and CD45 (mesenchymal stem cells), all from BD Biosciences, USA. Thirty-six female C57BL/6 mice (20–25 g) were randomly assigned to two groups. In the OVA group, mice were immunized using an adjuvant-free protocol by intraperitoneal injection of sterile ovalbumin (OVA, 10 μg OVA in 100 μl saline) on 7 alternate days. Forty days after the start of sensitization, 20 μg of OVA in 20 μl saline was instilled intratracheally. This procedure was performed 3 times with 3-day intervals between applications (Xisto et al., 2005). The control group (C) received saline using the same protocol. The C and OVA groups were further randomized to receive saline solution (0.