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Expression of Human Hormone-Sensitive Lipase (HSL) in Postmeiotic Germ Cells Confers Normal Fertility to HSL-Deficient Mice

Service of Medical Genetics (S.P.W., K.S., H.B., G.A.M.), Hôpital Sainte-Justine, Montréal, Québec H3T 1C5, Canada; Department of Anatomy and Cell Biology (S.C., L.H.), McGill University, Montréal, Québec, Canada, H3A 2B2; and Departments of Pediatrics, Human Genetics, and Pharmacology and Therapeutics (J.T.), McGill University and the Montreal Children’s Hospital, Montréal, Québec, Canada H3H 1P3

Address all correspondence and requests for reprints to: Grant A. Mitchell, M.D., Service of Medical Genetics, Hôpital Sainte-Justine, 3175 Chemin Côte Ste-Catherine, Montréal, Québec, Canada H3T 1C5. E-mail: grant.mitchell{at}recherche-ste-justine.qc.ca.

Hormone-sensitive lipase (HSL, Lipe, E.C.3.1.1.3) is a multifunctional fatty acyl esterase that is essential for male fertility and spermatogenesis and that also plays important roles in the function of adipocytes, pancreatic ß-cells, and adrenal cortical cells. Gene-targeted HSL-deficient (HSL–/–) male mice are infertile, have a 2-fold reduction in testicular mass, a 2-fold elevation of the ratio of esterified to free cholesterol in testis, and unique morphological abnormalities in round and elongating spermatids. Postmeiotic germ cells in the testis express a specific HSL isoform. We created transgenic mice expressing a normal human testicular HSL cDNA from the mouse protamine-1 promoter, which mediates expression specifically in postmeiotic germ cells. Testicular cholesteryl esterase activity was undetectable in HSL–/– mice, but in HSL–/– males expressing the testicular transgene, activity was 2-fold greater than normal. HSL transgene mRNA became detectable in testes between 19 and 25 days of age, coinciding with the first wave of postmeiotic transcription in round spermatids. In contrast to nontransgenic HSL–/– mice, HSL–/– males expressing the testicular transgene were normal with respect to fertility, testicular mass, testicular esterified/free cholesterol ratio, and testicular histology. Their cauda epididymides contained abundant, normal-appearing spermatozoa. We conclude that human testicular HSL is functional in mouse testis and that the mechanism of infertility in HSL-deficient males is cell autonomous and resides in postmeiotic germ cells, because HSL expression in these cells is in itself sufficient to restore normal fertility.

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