Search

The testis homogenate from Red bull (3-17 months of age) show specific binding of hLH and hFSH with Kd of 1.3 +/- 0.1 X 10(-10)M and 1.5 +/- 0.1 X 10(-9)M, respectively. Prepubertal bulls (3-5 3/4 months) exhibit the highest binding capacity of both LH and FSH, revealing the fact that LH and FSH receptors are present in high concentrations prior to the first rise in plasma T. The testicular T concentration was significantly higher in the four prepubertal bulls than in the four older animals in spite of the fact that circulating T is lower before puberty. Thus, local androgen effects within the testis may occur before peripheral androgenization. The prepubertal bull Leydig cell also displayed steroidogenic capacity. The ratio of biologically active (testosterone, dihydrotestosterone) to inactive androgens (androstenedione) increased as the animals approached puberty. Such qualitative changes in steroid production may be one of the factors responsible for peripheral androgenization.

Soluble Mn2+-dependent adenylate cyclase (MnAC) activity was found in testicular cytosol from blue foxes castrated during the breeding season. The rate of MnAC activity was approximately constant for 30 min at 35 degrees C and for 2 hr after storage at 25 degrees C. Activity was directly proportional to cytosol protein concentration and was optimal in the physiological pH range. Enzyme activity declined in the presence of an alkylating agent (N-ethyl maleimide, NEM) and was eliminated at a concentration of 1 mM NEM. Low concentrations (0.1-10 mM) of a reducing agent (beta-mercapto ethanol, beta ME) did not increase MnAC activity, whereas a high concentration (100 mM) led to a significant reduction (p less than 0.01) in activity. Substitution of Mn2+ in the assay medium with Mg2+ led to a total loss of enzyme activity, which could not be regained by adding hormones or by preincubation of cytosol for 60 min. The Km for Mn2+ was estimated to be 3.5 mM. The affinity of the enzyme for Mn2+ was not altered by varying the concentration of ATP. In contrast, increasing concentrations of Mn2+ appeared to increase the affinity of the enzyme for MnATP2-. The Km for MnATP2- thus varied from 6 to 18 mM.

An examination of the activity of the Mn2+-dependent adenylyl cyclase (AC) in fine needle biopsies from human testes was made. Simultaneously the DNA distribution patterns in suspensions of testicular cells derived from the same patients have been determined. The DNA distribution patterns were estimated by microflow fluorimetry (MFF) after straining with fluorochrome (ethidium bromide). Thus, AC activity could be assessed and correlated with the relative number of haploid (1C = spermatids), diploid (2C = spermatogonia and testicular somatic cells), and tetraploid (4C = primary spermatocytes) cells. Testicular Mn2+-dependent AC activities varied between 0 and 8.4 pmol cyclic adenosine monophosphate (cAMP)/mg protein/min and were highly correlated with the contents of haploid (1C) germ cells (spermatids) (r = 0.62, p less than 0.01). There was no correlation between Mn2+-dependent AC activity and diploid or tetraploid cells. This indicates that the Mn2+-dependent AC activity in the human testis, like in the rat and mouse, may be exclusively localized to haploid germ cells. An inverse correlation between plasma FSH and Mn2+-dependent AC activities indicated reduced inhibin secretion in situations where the Sertoli cells did not maintain the testicular germ cell production.

Adenylyl cyclase (AC) and protein carboxyl methylase (PCM) activities in human ejaculated spermatozoa were measured in 31 men being evaluated for infertility at the Infertility Clinic. The spermatozoal Mn2+-sensitive AC activities ranging between zero and 1.4 nmol cyclic adenosine monophosphate (cAMP)/10(9) cells/min, was positively correlated with motility index [% motile sperm X degree (0-4)] (r = 0.72, rho less than 0.05). This confirms a role for cAMP in human sperm motility. PCM activities, ranging between zero and 160 pmoles (CH3OH/10(9) cells/min), were significantly correlated with AC activities (r = 0.86, p less than 0.001). However, PCM activities were not positively correlated with motility index (p = 0.065). PCM most probably is a factor involved in spermatozoal motility since two patients suffering necrospermia possessed spermatozoa deficient in both AC and PCM activities.

The effects of prolactin and 2-bromo-alpha-ergocryptine (CB-154) on Leydig cell function in intact and hypophysectomized male rats were studied. The conclusions can be summarized as follows: prolactin (1) has a direct stimulatory effect on the number of LH receptors on rat Leydig cells, (2) has no effect on the characteristics of the dose-response curve of isolated Leydig cells (hCG stimulated androgen production) in vitro even after treatment with pharmacological doses in vivo, and (3) acts synergistically with LH to stimulate the quantity of androgen produced by the Leydig cells in response to hCG in vitro and to increase the sensitivity of the hCG-dose-response curve. Treatment of intact rats with CB-154 reduced the quantity of androgen produced by the Leydig cells in vitro after exposure to hCG and decreased LH binding to the same cells by 50%. These results suggest that under normal conditions, endogenous prolactin plays a key role in maintaining the functional integrity of rat Leydig cells.

Growth during adolescence was analyzed in 40 children with slipped capital femoral epiphysis using the Infancy Childhood Puberty growth model. The advantage of this model is that reference values for height can be adjusted for the individual age at pubertal maturation. In both sexes an above average height was found before the onset of the pubertal growth spurt. However, the pubertal gain in height was less than normal, and at maturity the heights were only slightly above the reference mean values. Most of the children had their first hip symptoms during the period of increasing gain in height at the initial stage of the pubertal growth spurt. Both boys and girls were overweight before puberty and remained so during puberty and at maturity.

The physicochemical and molecular properties of testicular Protein Carboxyl Methylase (PCM) have been studied. The testicular enzyme was stable at high ionic strength, independent of metal ions and resistant to reducing or alkylating agents, and displayed a narrow pH optimum of pH 5.8-6.0. The enzyme had a molecular weight of approximately 25,000 daltons and a Km for S-adenosyl-L-methionine (SAM) of 1.3 microM. Varying concentrations of gelatine (exogenous methyl acceptor protein) did not change the affinity of the enzyme for SAM. The molecular properties of the enzyme were characterized using gel filtration, hydroxyapatite and DEAE-cellulose chromatography, and isoelectric focusing. Three charge isomers exhibiting PCM activity were isolated with pI values of 6.1, 6.7, and 7.35 while comparative data from the pituitary gland revealed primarily the presence of the most acid isozyme (pI 6.1). These results suggest that the different testicular charge isozymes may be involved in the selective methylation of specific testicular proteins.

We have examined the hormonal regulation of the secretion of lactate and pyruvate from cultured rat Sertoli cells. FSH and isoproterenol caused 3-6-fold stimulation of lactate and pyruvate secretion, whereas ovine LH, TSH, and prolactin were ineffective. Dibutyryl cyclic AMP (10(-4) M) stimulated the secretion of lactate and pyruvate to the same extent as FSH. Much lower stimulation was observed when Sertoli cells from 43-day old rats were exposed to FSH or isoproterenol. FSH increased lactate secretion in a concentration-dependent manner. The concentration of FSH (NIH-S14) causing half-maximal stimulation of lactate secretion (150 ng/ml) was similar to that causing 50% maximal stimulation of Sertoli cell adenylyl cyclase. Both FSH and isoproterenol caused a time-dependent increase in lactate levels in the incubation medium during the first 6-9 hr after the addition of hormones, after which levels were constant or decreased. Thus, the production of lactate and pyruvate by cultured Sertoli cells is stimulated both by FSH and isoproterenol and these effects are exerted via cyclic AMP.

In the present study we have examined the soluble Mn2+ dependent, germ cell specific adenylyl cyclase (AC) activity and germ cell morphology in testicular biopsies from twenty-three boys, aged 2-17 years, with undescended testes and three adult men with normally descended testes. Eight of the boys were treated with hCG immediately before surgery. Germ cell AC-activity (3.2-3.4 pmoles cAMP/mg protein/min) was found in the adult testes with normal germ cell morphology. Furthermore, low but significant AC-activity (0.2-0.8 pmoles cAMP/mg protein/min) was noted in biopsies containing only primary spermatocytes. There was no Mn2+ dependent AC-activity in Sertoli cell only testes or in testes where only spermatogonia were observed. Treatment with hCG did not influence germ cell maturation or soluble Mn2+ dependent AC-activity.

Physicochemical properties of the soluble Mn2+-dependent adenylate cyclase (MnAC) in the blue fox testis were examined. MnAC activity in the cytosol fraction (106,000 g) migrated in a linear sucrose gradient as a single peak with a sedimentation coefficient (S20,W) of 4.2 Gel filtration on a Sephadex G-200 column revealed an Einstein-Stokes radius of 28 A and a frictional ratio of 1.15, indicating a molecular weight of approximately 51,000. The MnAC migrated as a single peak of activity during polyacrylamide gel electrophoresis with an Rf of 0.52. The isoelectric point (pI) estimated by isoelectric focusing was 5.5.

The properties (association and dissociation rates, affinity and specificity) of GnRH receptors in the rat pituitary and the Leydig cells are very similar. In addition, in vivo administration for 5 or 11 days of 10 micrograms of GnRH to adult rats resulted in an increase (p less than 0.01) in both Leydig cell and pituitary GnRH receptors. In contrast, the same treatment caused a significant decrease (p less than 0.01) of Leydig cell LH receptor number. Furthermore, testosterone propionate (500 micrograms/day), which had no effect on Leydig cell LH receptors, caused a significant increase (p less than 0.01) of testicular GnRH receptors but a decrease (p less than 0.01) of pituitary GnRH receptors. Estradiol 17 beta valerate (5 micrograms/day) reduced (p less than 0.01) both testicular (5 days) and pituitary (5 and 11 days) GnRH receptors. Such treatment for 5 days also decreased (p less than 0.05) the Leydig cell LH receptors. No effect of dexamethasone and 17-hydroxyprogesterone was seen after 5 or 11 days of treatment. Thus, although pituitary and Leydig cell receptors appear similar, their regulation by exogenous hormone treatments is different. Furthermore, the regulation of Leydig cell GnRH and LH receptors also appears very different, suggesting different roles of the receptors in the control of the Leydig cell function.

Particulate and Triton X-100 solubilized receptors for luteinizing hormone (LH) in the pig and bull testis were studied. In some of the experiments tissue from the rat testis was included for comparison. LH receptors in the bull and pig revealed very similar association and dissociation kinetics, affinity (Kd = 1.2-1.8 x 10(-10) M), stability and physicochemical properties. Binding capacity was higher in the pig (73 fmol/mg protein) than in the rat (33 fmol/mg protein) and bull (17 fmol/mg protein). Hormone binding stabilized the receptor against thermal denaturation and temperature stability decreased upon solubilization. It is concluded that the properties of the testicular LH receptor of the pig and bull are very similar to those previously described from the rat.

A single s.c. injection of 75 IU of human chorionic gonadotropin (hCG) into adult male rats caused a transient desensitization of the LH/hCG responsive adenylyl cyclase (AC) in membrane particles from rat testis. Two hours after the injection of hCG, LH/hCG responsive AC was reduced by 40%, whereas LH binding was still normal. After 24 hr LH/HCG responsive AC was lost, whereas LH binding only showed a marginal decrease. During the next 2-3 days there was a gradual loss of LH/HCG receptors, which reached a nadir at day 4 (14% of control levels). At day y and 9 following the hCG injection LH/hCG receptors and LH/hCG responsive AC gradually returned towards normal. Fluoride (F-) stimulated AC activity showed only minor changes throughout the period investigated. The initial loss of AC responsiveness to hCG was associated with maximal levels of circulating hCG. However, desensitization persisted for several days after hCG was cleared form the circulation. AC desensitization preceded LH receptor downregulation and may support the notion that uncoupling of the catalytic subunit of the AC from Leydig cell LH/hCG receptors is a requirement for subsequent receptor internalization.

The variation of the specific Mn2+-dependent adenylyl cyclase (AC activity in spermatids and follicle stimulating hormone (FSH)-responsive AC activities in Sertoli cells in different stages (I-XIV) of the seminiferous epithelial cycle has been investigated. Maximal Mn2+-dependent AC activity was observed in stages II-III while minimal activity was encountered in stages VII-VIII (spermiation). FSH-responsive AC activity exhibited a pattern that coincided with that of the Mn2+-dependent AC. The stage-dependent variation in spermatid AC activity cannot be explained by altered numbers of haploid cells. This raises the question whether the Sertoli cells may regulate the spermatid AC activity. Sertoli cells in various stages are all exposed to the same concentration of circulatory hormones. Hence the stage-dependent difference in FSH-responsiveness indicates that local influences (from germ cells?) may regulate the response of the AC in Sertoli cells to FSH.

Changes in the proportion of cells within various DNA classes of dispersed testicular cells from the developing rat were monitored by microflow fluorometry and correlated with changes in the function of the pituitary (FSH), of the Leydig cells (androgens) and Sertoli cells (androgen-binding proteins, ABP). Peaks of androgens and of FSH appeared simultaneously and coincided with an accumulation of tetraploid cells and with the first appearance of haploid cells in the testis and ABP in the epididymis. Estrogen treatment (5 micrograms/day) of developing rats from day 7 completely prevented the appearance of haploid cells in the testis as well as ABP in the epididymis. In these animals the wave of tetraploid cells started and progressed normally, indicating that transformation and progression of germinal cells to the stage of the primary spermatocytes were taking place. A combined treatment with FSH and dihydrotestosterone propionate (DHTP) resulted in a premature start of Sertoli cell secretion of ABP into the epididymis, but in a normal appearance of haploid and tetraploid cells. The time correlation between peaks in FSH/androgens, the start of Sertoli cell secretion, and the occurrence of haploid cells in the testis stresses the importance of these two hormones for normal Sertoli cell function and the importance of a functional Sertoli cell for the completion of meiosis.

Measurements of total rat testicular protein carboxyl-methylase (PCM) activity at various ages ranging from 10 to 90 days showed a rapid (fivefold) increase between 20 and 30 days, coincident with the occurrence of haploid germ cells. When partially purified testicular enzyme, at different ages, was fractionated by isoelectric focusing, the activity of the individual PCM isomers displayed clear differences in the time at which maximal activity was reached. The most acid PCM isoenzyme (pI 6.1) was the dominant isoform in the immature testis and exhibited the highest increase in activity between 20 and 30 days of age. During the same age interval, the activity of the other two isoenzymes (pI 6.7 and 7.4) increased only slightly. At 50 days, while the isofocusing profile revealed no additional increase in the activity of the acid isoform (pI 6.1) and only a doubling in the activity of the second isomer (pI 6.7), the most basic isoenzyme displayed a drastic increment in specific activity (approximately sixfold when compared to 30 days). This indicates that the PCM isozymes have different cellular localization in the seminiferous tubules. The acid isomer (pI 6.1) appears to be associated to the early stages of spermatogenesis and may represent both germ cell and somatic cell PCM. The basic isomer (pI 7.4) may be specific for germ cells (spermatids), and is most likely associated with the later stages of germ cell maturation.

Sertoli cell monolayers were prepared from 19-day-old rat testes. On day 7 of culture cells were incubated for 24 hr in the presence or absence of ovine follicle stimulating hormone (oFSH). Cells were harvested, and adenylyl cyclase responses of the membrane particles to FSH, human chorionic gonadotropin (hCG), isoproterenol, and fluoride (F-) were examined in the presence of either GTP or the nonhydrolyzable guanylyl nucleotide GMP-P(NH)P. Culturing the cells in presence of FSH caused a hormone specific desensitization of FSH-responsive adenylyl cyclase, whereas responses to isoproterenol and fluoride were unaffected. Activation of Sertoli cell adenylyl cyclase by GTP and GMP-P(NH)P showed no difference between cells preincubated with or without FSH, indicating that FSH did not change the activity of the G/F (or N) component or its interaction with the catalytic subunit of the adenylyl cyclase. FSH-responsive adenylyl cyclase in cultured Sertoli cells has been shown to be selectively desensitized by homologous hormone. The mechanism may involve alteration or loss of the FSH receptor or changes in the "coupling" of the FSH receptors to the G/F component of the adenylyl cyclase, since there was no alteration in the guanylyl nucleotide and fluoride activation.

Membrane-bound adenylate cyclase (AC) activity was much higher in the presence of Mn2+ than of Mg2+. The Mn2+-sensitive adenylate cyclase (MnAC) showed a linear rate of activity for at least 60 min. In contrast, the Mg2+-sensitive AC (MgAC) displayed a considerable burst in activity, so that after 90 min of activity it was approximately tenfold higher than at the start of incubation. Guanine nucleotides enhanced MgAC activity; 10(-6) to 10(-5) M of 5'-guanylylimidodiphosphate caused a threefold stimulation. The MgAC could be stimulated by hormones (FSH, hCG, PGE1, isoproterenol, glucagon), the highest activation being achieved with FSH. Increasing levels of ATP produced a concentration-dependent increase in MgAC activity. The apparent affinity of the AC for MgATP increased threefold (Km 0.50-0.15 mM) by raising the free Mg2+ concentration from 0.4 to 10.0 mM. The membrane-bound AC of the blue fox testis is thus regulated by hormones, Mg2+, and guanine nucleotides in a similar manner to ACs in other somatic cells and in testes from other species. The high MnAC activity in membrane particles from these testes probably represents membrane-bound AC activity in germ cells. The burst in MgAC activity during incubation may represent proteolytic activation of membrane-bound germ cell AC, with a gradual appearance of Mg2+ sensitivity.

Injection of high doses of FSH causes a partial desensitization of the FSH-responsive adenylyl cyclase (AC) in adult rat testes. The loss of responsiveness to FSH is dependent on time. Two hours after injection of one dose of human FSH (256 micrograms hFSH-PT2) in vivo, no effect was seen on FSH-stimulated AC activity (Km and maximal activation). After 24 hr there was an approximately 40% decrease in FSH activated AC. Injection of two doses of FSH (256 micrograms hFSH-PT2) 24 and 48 hr before being killed, gave a loss in FSH-responsive AC activity of approximately 60%. The decreased FSH-stimulated AC activity after FSH injections in vivo was associated with a comparable decrease in specific FSH binding. Whether this is a reflection of receptor occupancy or down regulation of the number of FSH receptors is not known. Desensitization of the FSH-responsive AC caused by FSH was not associated with a change in its Km.

Carnitine concentration was measured in human tissue obtained at surgery or autopsy. In all patients, the concentration of carnitine (nMol. g-1 tissue) was higher in epididymis than in testis, vas deferens, prostate, and seminal vesicles. There was no correlation between the tissue levels of testosterone in the testis and the concentration of carnitine in epididymis. As in the rat and baboon, carnitine is also found in high concentrations in the human epididymis.

The assay for cyclic nucleotide phosphodiesterase has been applied, with certain modifications, to the measurement of the soluble forms of these enzymes in the rat testis. The homogenization and incubation conditions were adjusted to achieve linear product formation as a function of time and protein concentrations and the resulting products were isolated by ion exchange chromatography using 5 mM HCl as the eluting agent. Phosphodiesterase activities were present in the testicular cytosol (105,000 g supernatant) of adult rats which were capable of hydrolyzing cAMP with a high (Km2 microM) and low Km20 microM) affinity and GMP with a relatively high affinity (Km3 microM). The low affinity cAMP enzyme activity could be stimulated with divalent ions such as calcium, magnesium, and manganese. At 18 days of age, all three enzyme activities were present in the testis, although both the high and low affinity cAMP phosphodiesterase displayed maximal rates (Vmax) that were only one third of the adult testis (when expressed per mg protein).

The case of a 74-year-old woman with the rare popliteal pterygium syndrome is presented. This syndrome is inherited as an autosomal dominant trait with incomplete penetrance and varying expression and consists of cleft lip and palate, lip pits, genital anomalies, popliteal pterygium, and malformations of the extremities. The various treatments our patient underwent over the years are reported. Treatment of popliteal pterygium involves special problems whem removing the skin fold because the nerve and vascular cords lie immediately anterior to the posterior fibrous cord. In the present case there are widespread arthrotic changes, both in the extremity joints and in the spine. These patients are short in stature. This, together with the general arthropathy, suggests a hereditary metabolic disturbance in the cartilaginous tissue.