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Isolation and Culture of Cells from the Nephrogenic Zone of the Embryonic Mouse Kidney
Published on: April 22, 2011
Expression of Bcl-2 and Bax in mouse renal tubules during kidney development
Xiao-Feng Song1, Hao Ren, Arne Andreasen
1Department of Histology and Embryology, Institute of Pathology and Pathophysiology, China Medical University, Shen Yang, Liao Ning, China.
Abstract:
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.
Insights
Bcl-2 and Bax proteins are key in kidney development, showing distinct expression patterns in proximal and distal tubules. Their varied localization suggests differing mitochondrial functions during kidney tubulogenesis.
Area of Science:
- Developmental Biology
- Cell Biology
- Mitochondrial Biology
Background:
- Bcl-2 and Bax are crucial regulators of apoptosis, cell adhesion, and migration.
- These proteins are structurally and functionally linked to mitochondria.
- Understanding their role in kidney development requires precise localization data.
Purpose of the Study:
- To determine the spatiotemporal expression patterns of Bcl-2 and Bax during mouse kidney development.
- To correlate protein expression with specific kidney structures and developmental stages.
Main Methods:
- Utilized kidneys from embryonic and postnatal mice (E16-21, P1-21).
- Employed computer-assisted 3D tubule tracing on E17 kidneys.
- Developed and applied an immunohistochemical technique on glutaraldehyde-fixed, plastic-embedded sections for precise localization.
Main Results:
- Strong Bcl-2 and Bax expression observed in mature proximal convoluted tubules across all time points.
- Weaker expression noted in proximal straight and immature proximal tubules, with minimal expression in distal tubules.
- No expression detected in early developing structures like ureteric buds, comma bodies, S-shaped bodies, and glomeruli.
Conclusions:
- Bcl-2 and Bax exhibit differential expression in proximal versus distal tubules during kidney development.
- This distinct localization suggests potential differences in mitochondrial function between mature proximal tubules and other tubular segments.
- The precise functional significance of Bcl-2 and Bax in tubulogenesis warrants further investigation.

