دورية أكاديمية

Targeting nuclear receptor corepressors for reversible male contraception.

التفاصيل البيبلوغرافية
العنوان: Targeting nuclear receptor corepressors for reversible male contraception.
المؤلفون: Suk-Hyun Hong, Castro, Glenda, Wang, Dan, Nofsinger, Russell, Kane, Maureen, Folias, Alexandra, Atkins, Annette R., Yu, Ruth T., Napoli, Joseph L., Sassone-Corsi, Paolo, de Rooij, Dirk G., Liddle, Christopher, Downes, Michael, Evans, Ronald M.
المصدر: Proceedings of the National Academy of Sciences of the United States of America; 2/27/2024, Vol. 121 Issue 9, p1-7, 19p
مصطلحات موضوعية: MALE contraceptives, ORAL contraceptives, THYROID hormone receptors, CONTRACEPTION, ORAL drug administration, RETINOIC acid receptors, HISTONE deacetylase inhibitors, SEMINIFEROUS tubules, FAMILY planning
مستخلص: Despite numerous female contraceptive options, nearly half of all pregnancies are unintended. Family planning choices for men are currently limited to unreliable condoms and invasive vasectomies with questionable reversibility. Here, we report the development of an oral contraceptive approach based on transcriptional disruption of cyclical gene expression patterns during spermatogenesis. Spermatogenesis involves a continuous series of self-renewal and differentiation programs of spermatogonial stem cells (SSCs) that is regulated by retinoic acid (RA)-dependent activation of receptors (RARs), which control target gene expression through association with corepressor proteins. We have found that the interaction between RAR and the corepressor silencing mediator of retinoid and thyroid hormone receptors (SMRT) is essential for spermatogenesis. In a genetically engineered mouse model that negates SMRT-RAR binding (SMRTmRID mice), the synchronized, cyclic expression of RAR-dependent genes along the seminiferous tubules is disrupted. Notably, the presence of an RA-resistant SSC population that survives RAR de-repression suggests that the infertility attributed to the loss of SMRT-mediated repression is reversible. Supporting this notion, we show that inhibiting the action of the SMRT complex with chronic, low-dose oral administration of a histone deacetylase inhibitor reversibly blocks spermatogenesis and fertility without affecting libido. This demonstration validates pharmacologic targeting of the SMRT repressor complex for non-hormonal male contraception. [ABSTRACT FROM AUTHOR]
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قاعدة البيانات: Complementary Index
الوصف
تدمد:00278424
DOI:10.1073/pnas.2320129121