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Endocrinology Vol. 140, No. 4 1709-1717
Copyright © 1999 by The Endocrine Society

ARTICLES

Single Exposure to Heat Induces Stage-Specific Germ Cell Apoptosis in Rats: Role of Intratesticular Testosterone on Stage Specificity1

Yah-He Lue, Amiya P. Sinha Hikim, Ronald S. Swerdloff, Paul Im, Khay Seng Taing, Tan Bui, Andrew Leung and Christina Wang

Division of Endocrinology, Department of Medicine, Harbor-University of California-Los Angeles Medical Center (Y.-H.L. A.P.S.H., R.S.S., A.L., C.W.), Torrance, California 90509; and California Academy of Mathematics and Science (P.I., K.S.T., T.B.), Carson, California 90747

Address all correspondence and requests for reprints to: C. Wang, M.D., Clinical Study Center, Box 16, Harbor-University of California-Los Angeles Medical Center, 1000 West Carson Street, Torrance, California 90509. E-mail: wang{at}gcrc.humc.edu

Short term exposure of the testis to heat causes degeneration of germ cells. However, the mechanisms underlying this process are poorly understood. The major objectives of this study were to determine whether the heat-induced loss of germ cells in the adult rat occurs via apoptosis, to document its stage-specific and cell-specific distribution, and to examine whether intratesticular testosterone (T) plays any role in the stage specificity of heat-induced germ cell death. Testes of adult male Sprague-Dawley rats were exposed to 22 C (control) or 43 C for 15 min. Animals were killed on days 1, 2, 9, and 56 after heat exposure. Germ cell apoptosis was characterized by DNA gel electrophoresis and in situ terminal deoxynucleotidyl transferase-mediated deoxy-UTP nick end labeling assay. The incidence of germ cell apoptosis [apoptotic index (AI)] was quite low in control rats (AI = 0.04–0.1). Mild hyperthermia within 1 or 2 days resulted in a marked activation (AI = 4.7–5.6) of germ cell apoptosis predominantly at early (I–IV) and late (XII–XIV) stages. Stages V–VI and VII–VIII were relatively protected from heat-induced apoptosis. Spermatocytes, including pachytenes at stages I–IV and IX–XII, diplotene and dividing spermatocytes at stages XIII–XIV, and early (steps 1–4) spermatids, were most susceptible to heat. On day 9, the majority of the tubules were severely damaged and displayed only a few remaining apoptotic germ cells. By day 56, spermatogenesis was completely recovered, and the incidence of germ cell apoptosis was compatible with the control levels. To determine whether intratesticular T plays a role in protecting germ cells at stages VII–VIII against heat-induced cell death, adult rats were exposed to local testicular heating on day 2 or were given a daily sc injection of GnRH antagonist (GnRH-A) for 4 days with and without a single exposure of testes to heat applied on day 2. By day 4, the incidence of increased germ cell apoptosis at stages other than VII–VIII were not different between heat-treated and GnRH-A- plus heat-treated groups, whereas the control group and the group treated with GnRH-A alone showed minimal apoptosis. GnRH-A addition to heat resulted in a further increase in apoptosis (by 3.2-fold) at stages VII–VIII over the values measured in the heat-treated group, and it became comparable to that at all other stages. Collectively, these results provide evidence that 1) heat induces germ cell apoptosis in a stage-specific and cell-specific fashion; and 2) intratesticular T plays a pivotal role in protecting germ cells at stages VII–VIII against heat-induced cell death. However, the possible involvement of various other factors, including growth factors, thermoprotectants, cytokines, and various death-related proteins, in protecting germ cells against heat-induced apoptosis cannot be ruled out.




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