Global Deletion of ALDH1A1 and ALDH1A2 Genes Does Not Affect Viability but Blocks Spermatogenesis.
| Autor: | Topping T; School of Molecular Biosciences, College of Veterinary Medicine, Washington State University, Pullman, WA, United States., Griswold MD; School of Molecular Biosciences, College of Veterinary Medicine, Washington State University, Pullman, WA, United States. |
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| Jazyk: | angličtina |
| Zdroj: | Frontiers in endocrinology [Front Endocrinol (Lausanne)] 2022 Apr 28; Vol. 13, pp. 871225. Date of Electronic Publication: 2022 Apr 28 (Print Publication: 2022). |
| DOI: | 10.3389/fendo.2022.871225 |
| Abstrakt: | The transition of undifferentiated A spermatogonia to differentiated spermatogonia requires the action of retinoic acid (RA). The synthesis of retinoic acid from retinal in the seminiferous epithelium is a result of the action of aldehyde dehydrogenases termed ALDH1A1, ALDH1A2, and ALDH1A3. We used a mouse with a global deletion of the Aldh1a1 gene that is phenotypically normal and the CRE -loxP approach to eliminate Aldh1a2 genes globally and from Sertoli cells and germ cells. The results show that global elimination of Aldh1a1 and Aldh1a2 genes blocks spermatogenesis but does not appear to affect viability. The cell specific elimination of Aldh1a2 gene showed that retinoic acid synthesis by Sertoli cells is required for the initial round of spermatogonial differentiation but that there is no requirement for retinoic acid synthesis by germ cells. In both the global gene deletion and the cell specific gene deletions the maintenance of Aldh1a3 activity could not compensate. Competing Interests: The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest. The reviewer KR declared a shared affiliation with the authors to the handling editor at the time of review. (Copyright © 2022 Topping and Griswold.) |
| Databáze: | MEDLINE |
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