Increasing testicular temperature by exposure to elevated ambient temperatures restores spermatogenesis in adult Utp 14b jsd mutant (jsd) mice

P. B. Comish, L. Y. Liang, Y. Yamauchi, C. C. Weng, G. Shetty, K. A. Naff, M. A. Ward, M. L. Meistrich

Research output: Contribution to journalArticlepeer-review

4 Scopus citations

Abstract

Because mutations in the human UTP14C gene are associated with male infertility, we sought to develop a method for fertility restoration in azoospermic mice with a mutation in the orthologous Utp14bjsd (jsd) gene that have spermatogonial arrest. The method is based on our observation that elevation of testicular temperatures restores spermatogonial differentiation in jsd mutant mice. To non-surgically raise intrascrotal temperatures we placed these mice in incubators at different elevated ambient temperatures. Exposure of jsd/jsd mice to ambient temperatures of 34.5 °C or 35.5 °C for 24 days increased the proportion of tubules with spermatocytes from 0% in untreated controls to over 80%. As those higher temperatures interfere with spermatid differentiation, the mice were then transferred to incubators at 32-32.5 °C for the next 24 days. These environments allowed differentiation to progress, resulting in up to 42% of tubules having late spermatids and about half of the mutant mice having spermatozoa in testicular suspensions. When these spermatozoa were used in intracytoplasmic sperm injection, all gave rise to viable healthy offspring with normal weight gain and fertility. The successful restoration of fertility in Utp14b mutant mice suggests that transient testicular warming might also be useful for spermatogenesis recovery in infertile men with UTP14C gene mutations.

Original languageEnglish (US)
Pages (from-to)376-384
Number of pages9
JournalAndrology
Volume3
Issue number2
DOIs
StatePublished - Mar 1 2015

Keywords

  • Azoospermia
  • Genetic disorders
  • Infertility
  • Intracytoplasmic sperm injection
  • Spermatogenesis

ASJC Scopus subject areas

  • Endocrinology, Diabetes and Metabolism
  • Reproductive Medicine
  • Endocrinology
  • Urology

MD Anderson CCSG core facilities

  • Research Animal Support Facility

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