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Published on: February 6, 2018
Apoptosis mediated by phosphatidylserine externalization in the elimination of aneuploid germ cells during human
L Garcia-Quevedo1, J Blanco, Z Sarrate
1Unitat de Biologia Cel·lular, Facultat de Biociències, Universitat Autònoma de Barcelona, Bellaterra (Cerdanyola del Vallès), Spain.
Abstract:
It has been described that aneuploidies trigger cell cycle checkpoints leading to apoptosis. The aim of this study was to assess the relationship between the presence of chromosomal abnormalities and apoptosis in germ cells and in Sertoli cells. Fourteen diagnostic testicular biopsies from infertile patients were processed following a sequential methodology, which included enzymatic disaggregation, apoptotic staining, cell sorting, cell fixation, and fluorescent in situ hybridization analysis. The chromosome constitution of germ cells (interphase pre-meiotic germ cells, meiotic figures, post-reductional germ cells, and spermatozoa) and Sertoli cells was evaluated in non-sorted and flow-sorted cell populations (apoptotic and viable). The mean percentage of aneuploidy was compared between the three fractions in each cell type using a Kruskal-Wallis test. If significant results were obtained, a two-by-two Chi-squared test was performed. There were significant differences between the apoptotic fraction and the viable and non-sorted fractions in the pre-meiotic germ cells (p < 0.01). In the remaining cell types, no association between the presence of aneuploidy and apoptotic processes was observed, even in the case of post-reductional germ cells in which we detected the highest rates of aneuploidy regardless of the fraction analyzed. From our data, it can be inferred that most of the aneuploid post-reductional germ cells are efficiently removed from the testicular epithelium without differentiating into spermatozoa. Our results suggest that the elimination of aneuploid testicular epithelial cells is triggered by different mechanisms. Accordingly, the cellular elimination of aneuploid germ cells beyond the blood-testis barrier does not involve phosphatidylserine externalization.
Insights
Aneuploidies, or chromosomal abnormalities, in germ cells are linked to apoptosis in pre-meiotic cells. However, most aneuploid germ cells are eliminated before becoming sperm, suggesting varied removal mechanisms.
Area of Science:
- Reproductive Biology
- Cell Biology
- Genetics
Background:
- Aneuploidies are known to induce cell cycle checkpoints, leading to programmed cell death (apoptosis).
- Understanding the link between chromosomal abnormalities and apoptosis in testicular cells is crucial for male fertility research.
Purpose of the Study:
- To investigate the relationship between chromosomal abnormalities (aneuploidy) and apoptosis in germ cells and Sertoli cells.
- To determine if aneuploid germ cells are eliminated through apoptosis before differentiating into spermatozoa.
Main Methods:
- Analyzed 14 testicular biopsies from infertile patients using enzymatic disaggregation, apoptotic staining, cell sorting, and fluorescent in situ hybridization.
- Evaluated chromosome constitution in sorted and non-sorted germ cells (pre-meiotic, meiotic, post-reductional, spermatozoa) and Sertoli cells.
- Compared aneuploidy percentages between apoptotic and viable cell fractions using Kruskal-Wallis and Chi-squared tests.
Main Results:
- A significant association between aneuploidy and apoptosis was found in pre-meiotic germ cells (p < 0.01).
- No significant association between aneuploidy and apoptosis was observed in other germ cell types or Sertoli cells.
- The highest rates of aneuploidy were detected in post-reductional germ cells, irrespective of the apoptotic fraction.
Conclusions:
- Most aneuploid post-reductional germ cells are effectively eliminated from the testicular epithelium before differentiating into spermatozoa.
- The elimination of aneuploid germ cells beyond the blood-testis barrier does not appear to involve phosphatidylserine externalization (a common apoptotic marker).
- Different mechanisms likely regulate the removal of aneuploid testicular epithelial cells.
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