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Apoptosis in the cortex of the developing mouse kidney.
Jonathan G D Foley1, Jonathan B L Bard
1Department of Biomedical Sciences, Edinburgh University, Edinburgh EH8 9XD, UK.
Journal of Anatomy
|December 20, 2002
Summary
Apoptosis levels in developing mouse kidneys are significantly lower than previously reported. This study reveals apoptosis is minimal in embryonic kidney development, similar to other tissues.
Area of Science:
- Developmental Biology
- Cell Biology
- Histology
Background:
- Published apoptosis levels in developing rat kidneys (approx. 2.5%) appear high for a tissue without apparent need for continuous cell death.
- Investigating apoptosis and mitosis in developing mammalian kidneys is crucial for understanding organogenesis.
Purpose of the Study:
- To quantify and characterize apoptosis and mitosis in the developing mouse kidney cortex.
- To compare apoptosis levels in wholemount versus cryosectioned embryonic kidney tissues.
- To determine if apoptosis levels in the embryonic kidney are typical of other developing mammalian tissues.
Main Methods:
- Confocal microscopy of wholemount embryonic mouse kidneys stained with propidium iodide.
- Analysis of nuclear morphology to count mitotic, apoptotic, and interphase nuclei.
- Comparison of apoptosis and mitotic indices in wholemount kidneys, tails, and lungs.
Main Results:
- The mean apoptotic index in wholemount embryonic mouse kidneys was 0.28%, approximately 10% of levels reported in cryosectioned rat kidneys.
- Mitotic index peaked at E14.5 (around 2-3%) and decreased to 0.5% by P14.
- Cryosectioning may artifactually inflate apoptosis measurements due to nuclear fragmentation.
Conclusions:
- Apoptosis levels in wholemount embryonic mouse kidney cortex are substantially lower than previously reported.
- The observed low level of apoptosis is typical for embryonic mouse tissues not requiring extensive cell death during development.
- Cryosectioning artifacts may account for discrepancies in previously reported apoptosis rates.