Ortega-Martínez Marta, Rodríguez-Flores Laura E, de-la-Garza-González Carlos, Ancer-Rodríguez Jesús, Jaramillo-Rangel Gilberto
Department of Pathology, School of Medicine, Autonomous University of Nuevo Leon, Monterrey, Nuevo Leon, Mexico.
Department of Embryology, School of Medicine, Autonomous University of Nuevo Leon, Monterrey, Nuevo Leon, Mexico.
J Cell Mol Med. 2015 Nov;19(11):2679-81. doi: 10.1111/jcmm.12653. Epub 2015 Aug 10.
Regeneration of the lung airway epithelium after injury has been extensively studied. In contrast, analysis of its turnover in healthy adulthood has received little attention. In the classical view, this epithelium is maintained in the steady-state by the infrequent proliferation of basal or Clara cells. The intermediate filament protein nestin was initially identified as a marker for neural stem cells, but its expression has also been detected in other stem cells. Lungs from CD1 mice at the age of 2, 6, 12, 18 or 24 months were fixed in neutral-buffered formalin and paraffin-embedded. Nestin expression was examined by an immunohistochemical peroxidase-based method. Nestin-positive cells were detected in perivascular areas and in connective tissue that were in close proximity of the airway epithelium. Also, nestin-positive cells were found among the cells lining the airway epithelium. These findings suggest that nestin-positive stem cells circulate in the bloodstream, transmigrate through blood vessels and localize in the lung airway epithelium to participate in its turnover. We previously reported the existence of similar cells able to differentiate into lung chondrocytes. Thus, the stem cell reported here might be a bone marrow-derived mesenchymal stem cell (BMDMSC) able to generate several types of lung tissues. In conclusion, our findings indicate that there exist a BMDMSC in healthy adulthood that participates in the turnover of the lung airway epithelium. These findings may improve our knowledge about the lung stem cell biology and also provide novel approaches to therapy for devastating pulmonary diseases.
肺气道上皮损伤后的再生已得到广泛研究。相比之下,其在健康成年期的更新分析却很少受到关注。按照传统观点,这种上皮通过基底细胞或克拉拉细胞的不频繁增殖维持在稳态。中间丝蛋白巢蛋白最初被鉴定为神经干细胞的标志物,但其表达也在其他干细胞中被检测到。将2、6、12、18或24月龄CD1小鼠的肺用中性缓冲福尔马林固定并石蜡包埋。采用基于免疫组织化学过氧化物酶的方法检测巢蛋白表达。在血管周围区域和靠近气道上皮的结缔组织中检测到巢蛋白阳性细胞。此外,在气道上皮内衬细胞中也发现了巢蛋白阳性细胞。这些发现表明,巢蛋白阳性干细胞在血液中循环,穿过血管迁移并定位于肺气道上皮以参与其更新。我们之前报道过存在能够分化为肺软骨细胞的类似细胞。因此,这里报道的干细胞可能是一种能够生成多种类型肺组织的骨髓间充质干细胞(BMDMSC)。总之,我们的研究结果表明,在健康成年期存在一种参与肺气道上皮更新的BMDMSC。这些发现可能会增进我们对肺干细胞生物学的了解,也为治疗严重肺部疾病提供新的方法。