Machado Mariana N, Mazzoli-Rocha Flavia, Casquilho Natália V, Maron-Gutierrez Tatiana, Ortenzi Victor H, Morales Marcelo M, Fortunato Rodrigo S, Zin Walter A
Laboratory of Respiration Physiology, Carlos Chagas Filho Institute of Biophysics, Universidade Federal do Rio de Janeiro, Rio de Janeiro, Brazil.
Laboratory of Immunopharmacology, Oswaldo Cruz Institute (FIOCRUZ), Rio de Janeiro, Brazil.
Front Physiol. 2018 Feb 20;9:121. doi: 10.3389/fphys.2018.00121. eCollection 2018.
Murine papain-induced emphysema is a model that reproduces many of the features found in patients. Bone marrow-derived mononuclear cells (BMMC) have already been used to repair the alveolar epithelium in respiratory diseases, but not in the papain model. Thus, we hypothesized that BMMC could prevent the pathophysiological processes in papain-induced experimental emphysema. Female BALB/c mice received intratracheal instillation of 50 μL of saline (S groups) or papain (P groups, 10 IU/50 μl of saline) on days 1 and 7 of the experimental protocol. On the 14th day, 2 × 10 BMMC of male BALB/c mice (SC21 and PC21) or saline (SS21 and PS21) were injected by the jugular vein. Analyses were done on days 14 (S14 and P14) and 21 (SS21, PS21, SC21, and PC21) of the protocol. qPCR evaluated the presence of the Y chromosome in the lungs of BMMC recipient animals. Functional residual capacity (FRC), alveolar diameter, cellularity, elastic fiber content, concentrations of TNF-α, IL-1β, IL-6, MIP-2, KC, IFN-γ, apoptosis, mRNA expression of the dual oxidase (DUOX1 and DUOX2), production of HO and DUOX activity were evaluated in lung tissue. We did not detect the Y chromosome in recipients' lungs. FRC, alveolar diameter, polymorphonuclear cells (PMN) and levels of KC, MIP-2, and IFN-γ increased in P14 and PS21 groups; the changes in the latter were reverted by BMMC. TNF-α, IL-1β e IL-6 were similar in all groups. The amount of elastic fibers was smaller in P14 and PS21 than in other groups, and BMMC did not increase it in PC21 mice. PS21 animals showed increased DUOX activity and mRNA expression for DUOX1 and 2. Cell therapy reverted the activity of DUOX and mRNA expression of DUOX1. BMMC reduced mRNA expression of DUOX2. Apoptosis index was elevated in PS21 mice, which was reduced by cell therapy in PC21. Static compliance, viscoelastic component of elastance and pressure to overcome viscoelasticity were increased in P14 and PS21 groups. These changes and the high resistive pressure found on day 21 were reverted by BMMC. In conclusion, BMMC showed potent anti-inflammatory, antiapoptotic, antioxidant, and restorative roles in papain-triggered pulmonary emphysema.
小鼠木瓜蛋白酶诱导的肺气肿是一种能重现患者多种特征的模型。骨髓来源的单核细胞(BMMC)已被用于修复呼吸系统疾病中的肺泡上皮,但未用于木瓜蛋白酶模型。因此,我们假设BMMC可以预防木瓜蛋白酶诱导的实验性肺气肿中的病理生理过程。在实验方案的第1天和第7天,雌性BALB/c小鼠经气管内滴注50 μL生理盐水(S组)或木瓜蛋白酶(P组,10 IU/50 μl生理盐水)。在第14天,通过颈静脉注射雄性BALB/c小鼠的2×10 BMMC(SC21和PC21)或生理盐水(SS21和PS21)。在实验方案的第14天(S14和P14)和第21天(SS21、PS21、SC21和PC21)进行分析。qPCR评估BMMC受体动物肺中Y染色体的存在情况。在肺组织中评估功能残气量(FRC)、肺泡直径、细胞密度、弹性纤维含量、TNF-α、IL-1β、IL-6、MIP-2、KC、IFN-γ的浓度、细胞凋亡、双氧化酶(DUOX1和DUOX2)的mRNA表达、HO的产生和DUOX活性。我们在受体肺中未检测到Y染色体。P14和PS21组的FRC、肺泡直径、多形核细胞(PMN)以及KC、MIP-2和IFN-γ水平升高;后者的变化被BMMC逆转。所有组中的TNF-α、IL-1β和IL-6相似。P14和PS21组的弹性纤维量比其他组少,并且BMMC在PC21小鼠中未增加其含量。PS21动物的DUOX活性以及DUOX1和2的mRNA表达增加。细胞治疗逆转了DUOX的活性和DUOX1的mRNA表达。BMMC降低了DUOX2的mRNA表达。PS21小鼠的细胞凋亡指数升高,而PC21中的细胞治疗使其降低。P14和PS21组的静态顺应性、弹性的粘弹性成分以及克服粘弹性的压力增加。这些变化以及第21天发现的高阻力压力被BMMC逆转。总之,BMMC在木瓜蛋白酶引发的肺气肿中显示出强大的抗炎、抗凋亡、抗氧化和恢复作用。