Department of Histology and Embryology, Institute of Pathology and Pathophysiology, China Medical University, Shen Yang, Liao Ning, China.
PLoS One. 2012;7(2):e32771. doi: 10.1371/journal.pone.0032771. Epub 2012 Feb 28.
Bcl-2 and Bax play an important role in apoptosis regulation, as well as in cell adhesion and migration during kidney morphogenesis, which is structurally and functionally related to mitochondria. In order to elucidate the role of Bcl-2 and Bax during kidney development, it is essential to establish the exact location of their expression in the kidney. The present study localized their expression during kidney development. Kidneys from embryonic (E) 16-, 17-, 18-day-old mouse fetuses, and postnatal (P) 1-, 3-, 5-, 7-, 14-, 21-day-old pups were embedded in Epon. Semi-thin serial sections from two E17 kidneys underwent computer assisted 3D tubule tracing. The tracing was combined with a newly developed immunohistochemical technique, which enables immunohistochemistry on glutaraldehyde fixated plastic embedded sections. Thereby, the microstructure could be described in detail, and the immunochemistry can be performed using exactly the same sections. The study showed that Bcl-2 and Bax were strongly expressed in mature proximal convoluted tubules at all time points, less strongly expressed in proximal straight tubules, and only weakly in immature proximal tubules and distal tubules. No expression was detected in ureteric bud and other earlier developing structures, such as comma bodies, S shaped bodies, glomeruli, etc. Tubules expressing Bcl-2 only were occasionally observed. The present study showed that, during kidney development, Bcl-2 and Bax are expressed differently in the proximal and distal tubules, although these two tubule segments are almost equally equipped with mitochondria. The functional significance of the different expression of Bcl-2 and Bax in proximal and distal tubules is unknown. However, the findings of the present study suggest that the mitochondrial function differs between mature proximal tubules and in the rest of the tubules. The function of Bcl-2 and Bax during tubulogenesis still needs to be investigated.
Bcl-2 和 Bax 在细胞凋亡调控以及肾脏形态发生过程中的细胞黏附和迁移中发挥重要作用,这与线粒体在结构和功能上有关。为了阐明 Bcl-2 和 Bax 在肾脏发育过程中的作用,必须确定它们在肾脏中的表达的确切位置。本研究定位了它们在肾脏发育过程中的表达。将来自胚胎 (E) 16、17、18 天龄的胎鼠和出生后 (P) 1、3、5、7、14、21 天龄的幼鼠的肾脏嵌入 Epon。从两个 E17 肾脏的半薄连续切片中进行计算机辅助的 3D 小管追踪。该追踪与新开发的免疫组织化学技术相结合,该技术可在戊二醛固定的塑料包埋切片上进行免疫组织化学染色。由此,可以详细描述微观结构,并可使用完全相同的切片进行免疫化学染色。该研究表明,Bcl-2 和 Bax 在所有时间点均在成熟的近端卷曲小管中强烈表达,在近端直小管中表达较弱,在未成熟的近端小管和远端小管中表达较弱。在输尿管芽和其他早期发育结构(如逗号体、S 形体、肾小球等)中未检测到表达。偶尔观察到仅表达 Bcl-2 的小管。本研究表明,在肾脏发育过程中,Bcl-2 和 Bax 在近端和远端小管中的表达不同,尽管这两个小管段几乎都配备有相等数量的线粒体。Bcl-2 和 Bax 在近端和远端小管中的不同表达的功能意义尚不清楚。然而,本研究的结果表明,成熟的近端小管和其余小管之间的线粒体功能不同。Bcl-2 和 Bax 在小管生成中的功能仍需要进一步研究。