Secretion of transferrin in ovine seminiferous tubule cell cultures in response to FSH: influence of breed, season of birth and age of lambs

1993 ◽  
Vol 5 (1) ◽  
pp. 83 ◽  
Author(s):  
C Monet-Kuntz ◽  
I Fontaine

The response of lamb Sertoli cells to follicle stimulating hormone (FSH) was investigated by measuring transferrin secretion in seminiferous tubule cell cultures throughout the non-pubertal and the prepubertal periods. Cells could be cultured from birth until they attained a testicular weight of 19 g. The characteristics of individual dose-response curves were compared according to the breed, season of birth and testicular weight of the lambs. At the same season of birth and within a given testis weight range, dose-response curves of Romanov and Ile-de-France lambs were similar. Within a given testis weight range, spring-born animals exhibited a higher maximal transferrin secretion than autumn-born lambs, but the ED50 was similar. The main factor of variation of the dose-response curve parameters was the testicular weight of the lambs: the amplitude of FSH response increased 3-fold from a testicular weight of 6 g onwards, i.e. from the appearance of spermatogonia in seminiferous tubules. The ED50 increased 5-fold from 11 g onwards, i.e. from the beginning of the prepubertal period. Thus, Sertoli cells become less sensitive to FSH as spermatogenesis develops in seminiferous tubules. This phenomenon is largely the result of higher phosphodiesterase activity and is greatly reduced by 1-methyl-3-isobutyl-xanthine (MIX).

Author(s):  
Rabah Mamou ◽  
Elara Moudilou ◽  
Jean-Marie Exbrayat ◽  
Mansour Amroun

The reproductive cycle of male wall lizard Podarcis vaucheri (Boulenger, 1905) living in Djurdjura mountain, was analyzed from April till October 2014. Its seasonal mixed-type cycle was characterized by three phases: sexual activity, quiescence and recrudescence. After the emergence of lizard from hibernation an intense sexual activity was observed in spring (April, May, and June) at which the testicular weight and seminiferous tubules diameter reached their maximal values. At this period, spermiogenesis was also maximal and the spermiation allowed the release of a large quantity of spermatozoa in both the seminiferous tubules and epididymis lumen. In July, a short sexual resting period followed, during which the testes mass and seminiferous tubules diameter decreased. Spermatogonia and some primary spermatocytes were observed against the wall of seminiferous tubules. The recrudescence period (August, September and October) was characterized by a progressive increase of the testis weight and seminiferous tubules diameter. Spermatocytogenesis began in August, and spermiogenesis occurred in September and October, before the diapause period. But the presence of spermatozoids was not signaled in the epididymis lumen. Field observations and microscopic evidence of testis showed that both sexes reproduced synchronously during spring and early summer.


1999 ◽  
Vol 145 (5) ◽  
pp. 1027-1038 ◽  
Author(s):  
Antonella Tripiciano ◽  
Carmelina Peluso ◽  
Anna Rita Morena ◽  
Fioretta Palombi ◽  
Mario Stefanini ◽  
...  

The potent smooth muscle agonist endothelin-1 (ET-1) is involved in the local control of seminiferous tubule contractility, which results in the forward propulsion of tubular fluid and spermatozoa, through its action on peritubular myoid cells. ET-1, known to be produced in the seminiferous epithelium by Sertoli cells, is derived from the inactive intermediate big endothelin-1 (big ET-1) through a specific cleavage operated by the endothelin-converting enzyme (ECE), a membrane-bound metalloprotease with ectoenzymatic activity. The data presented suggest that the timing of seminiferous tubule contractility is controlled locally by the cyclic interplay between different cell types. We have studied the expression of ECE by Sertoli cells and used myoid cell cultures and seminiferous tubule explants to monitor the biological activity of the enzymatic reaction product. Northern blot analysis showed that ECE-1 (and not ECE-2) is specifically expressed in Sertoli cells; competitive enzyme immunoassay of ET production showed that Sertoli cell monolayers are capable of cleaving big ET-1, an activity inhibited by the ECE inhibitor phosphoramidon. Microfluorimetric analysis of intracellular calcium mobilization in single cells showed that myoid cells do not respond to big endothelin, nor to Sertoli cell plain medium, but to the medium conditioned by Sertoli cells in the presence of big ET-1, resulting in cell contraction and desensitization to further ET-1 stimulation; in situ hybridization analysis shows regional differences in ECE expression, suggesting that pulsatile production of endothelin by Sertoli cells (at specific “stages” of the seminiferous epithelium) may regulate the cyclicity of tubular contraction; when viewed in a scanning electron microscope, segments of seminiferous tubules containing the specific stages characterized by high expression of ECE were observed to contract in response to big ET-1, whereas stages with low ECE expression remained virtually unaffected. These data indicate that endothelin-mediated spatiotemporal control of rhythmic tubular contractility might be operated by Sertoli cells through the cyclic expression of ECE-1, which is, in turn, dependent upon the timing of spermatogenesis.


2002 ◽  
Vol 126 (1) ◽  
pp. 64-69
Author(s):  
Manuel Nistal ◽  
María Luisa Riestra ◽  
Ricardo Paniagua

Abstract Objective.—To evaluate seminiferous epithelium lesions in adult cryptorchid testes showing lymphoid infiltrates in seminiferous tubules and interstitium (ie, focal orchitis). Also, to consider the possible role of this lesion in the etiology of tubular atrophy. Methods.—We performed a histopathologic study of the cryptorchid testes and adjacent epididymides removed from 50 adult men who had not been previously treated for cryptorchidism. The study included morphologic and semiquantitative evaluation of seminiferous tubule pathology (according to germ cell numbers), Sertoli cell morphology, tubular lumen dilation, rete testis pattern (normal, hypoplastic, or cystic), and epididymal pattern (normal or epididymal duct hypoplasia). The study also included immunohistochemical evaluation of immune cell markers. The results were compared with clinical and laboratory findings. Results.—Focal lymphoid infiltrates (mainly lymphocytes) in seminiferous tubules and interstitium were found in 22 patients (44%), all of whom had unilateral cryptorchidism. The course of orchitis was asymptomatic, and laboratory data were normal. According to the seminiferous tubule pathology, a variety of histopathologic diagnoses, were made: (1) mixed atrophy consisting of Sertoli cell–only tubules intermingled with tubules showing maturation arrest of spermatogonia (11 testes, 4 of which also showed hyalinized tubules); (2) Sertoli cell–only tubules plus hyalinized tubules (4 testes); (3) Sertoli cell–only tubules (3 testes); (4) intratubular germ cell neoplasia (2 testes, 1 of which also showed hyalinized tubules); (5) complete tubular hyalinization (1 testis); and (6) tubular hyalinization plus some groups of tubules with hypospermatogenesis (all germ cell types were present although in lower numbers, 1 testis). Dysgenetic Sertoli cells, that is, Sertoli cells that had undergone anomalous, incomplete maturation, were observed in all nonhyalinized seminiferous tubules with inflammatory infiltrates. Tubular ectasia was observed in 13 cases. The rete testis was hypoplastic and showed cystic transformation in 18 testes, and the epididymis was hypoplastic in 15 testes. Conclusions.—The causes of these focal inflammatory infiltrates are unknown. It is possible that tubular ectasia and Sertoli cell dysgenesis are involved and that these alterations cause a disruption of the blood-testis barrier and allow antigens to enter the testicular interstitium, giving rise to an autoimmune process.


1987 ◽  
Vol 116 (3) ◽  
pp. 413-417 ◽  
Author(s):  
D. Dubé ◽  
A. Assaf ◽  
G. Pelletier ◽  
F. Labrie

Abstract. After 4 months of treatment of adult male dogs with the GnRH agonist (GnRH-A) [D-Trp6]GnRH ethylamide, the seminiferous tubules contained only type A and B spermatogonia, Sertoli cells, and rare primary spermatocytes, thus causing a 64% decrease in testis weight. At the electron microscope level, Sertoli cells showed an increase in phagosomes and lipid droplets. Leydig cells were markedly atrophied with the accumulation of lipid droplets and showed a pre-dominance of mitochondria with lamellar instead of vesicular cristae. Four months after cessation of treatment with GnRH-A, a complete return to normal spermatogenesis and Leydig cell morphology was observed. The full reversibility of spermatogenesis in the dog after chronic GnRH-A treatment suggests that this well-tolerated peptide could be used as a reversible method of male contraception.


2019 ◽  
Vol 47 (1) ◽  
Author(s):  
Jéssica Aline Withoeft ◽  
Maísa Chicocca ◽  
Fábio Santiani ◽  
Leonardo Silva Da Costa ◽  
Karina Aline Mateus ◽  
...  

Background: Immunocastration is a less invasive and painless procedure compared to surgical castration, which causes greater stress to animals, especially when performed improperly. Immunocastration stimulates the production of antibodies against Gonadotropin-Releasing Hormone (GnRH), temporarily blocking the hormone production by the male gonads. Anatomopathological evaluation of animals submitted to immunocastration with the establishment of different degrees of testicular degeneration helps to evaluate the efficacy of the different dose ranges used for this procedure. Because of the scarcity of information about this procedure in young bulls, the study aimed to compare the immunocastrated and non-castrated animals.Materials, Methods & Results: Eighteen Angus-Limousin bulls were used from weaning (7 ± 1 months) to slaughtering (15 ± 1 months) with the establishment of two groups composed of nine non-castrated (NC) and nine immunocastrated (IC) animals. In the IC group, three doses of GnRH synthesis inhibitor vaccine (Bopriva®) were applied on days 0 (weaning), 87 and 223. At slaughter, scrotal circumference, weight (kg), width (cm), length (cm) and total size (width x length) of the testicles were obtained, then were routinely processed for histopathological analysis. Four degrees of testicular degeneration was established: grade 0 (no changes), grade 1 (mild), grade 2 (moderate) and grade 3 (severe). Statistical analysis was performed using Student's t-test to compare the means of macroscopic variables. The scrotal circumference started to decrease in the IC animals on day 132, with a certain growth from day 194. There was a significant difference between the two groups for width (P = 0.001), length (P = 0.004), total size (P = 0.003) and scrotal circumference (P = 0.04). Testicles of the IC group tended to be lighter (P = 0.06). The final difference between the groups was 6.3 cm for scrotal perimeter, with respective averages of 27.44 cm and 33.77 cm for the IC and NC group, respectively. In the microscopic evaluation, NC animals obtained grade 0. In the IC animals, 33.33% (3/9) had degeneration grade 1 with slight basement membrane tortuosity and Sertoli cell atrophy, 33.33% (3/9) obtained grade 2 with moderate tortuosity and thickening of seminiferous tubules, Sertoli and Leydig cell atrophy, and absence of spermatogenesis and 33.33% (3/9) reached grade 3, with decreased seminiferous tubules and a severe and diffuse atrophy of Leydig and Sertoli cells and complete absence of spermatogenesis, with a 1:5 ratio in seminiferous tubule diameter between NC and IC grade 3 animals, respectively.Discussion: There was a significant difference in several testicular macroscopic aspects between the two groups, similar to values using eight months old field-bred animals, with a difference of 8.78 cm between groups, also with the use of three doses of Bopriva. The only macroscopic variable that showed just a tendency of difference between the groups was testicular weight, whereas, in a study with crossbred animals with nine months old, there was a difference of 152 g in testicular weight between groups. Histologically, in immunocastrated two-year-old Nelore cattle, 85% demonstrated a total absence of spermatogenesis and 15% had a partial reduction, suggesting functional recovery of Sertoli cells after the last vaccination booster or partial inhibition of spermatogenesis. In this study, 90-day dose intervals produced effective immunization during 105 days, which is the suggested period for the third dose. The anatomopathological analysis proved to be effective for the comparison between the groups and the degree of the promoted degeneration.


1967 ◽  
Vol 13 (11) ◽  
pp. 1421-1425
Author(s):  
Robert B. Stewart ◽  
Sunidhkumar S. Gandhi

Repeated assays of standard preparations of interferon carried out for over a year using primary cultures of chick-embryo cells and Sindbis virus in an assay system showed that cell cultures varied in their sensitivity to interferon. This altered sensitivity was not due to a change in the challenge virus nor to the time of exposure of cells to interferon. An analysis of the data showed that the slope of the dose–response curves remained constant although they could be displaced, indicating changes in sensitivity. Information was also obtained demonstrating that sensitivity of cells to interferon could vary within a single assay.


Reproduction ◽  
2016 ◽  
Vol 151 (5) ◽  
pp. 527-538 ◽  
Author(s):  
M Faure ◽  
E Guibert ◽  
S Alves ◽  
B Pain ◽  
C Ramé ◽  
...  

Abstract Metformin, an insulin sensitiser from the biguanide family of molecules, is used for the treatment of insulin resistance in type 2 diabetes individuals. It increases peripheral glucose uptake and may reduce food intake. Based on the tight link between metabolism and fertility, we investigated the role of metformin on testicular function using in vitro culture of Sertoli cells and seminiferous tubules, complemented by in vivo data obtained following metformin administration to prepubertal chickens. In vitro, metformin treatment reduced Sertoli cell proliferation without inducing apoptosis and morphological changes. The metabolism of Sertoli cells was affected because lactate secretion by Sertoli cells increased approximately twofold and intracellular free ATP was negatively impacted. Two important pathways regulating proliferation and metabolism in Sertoli cells were assayed. Metformin exposure was not associated with an increased phosphorylation of AKT or ERK. There was a 90% reduction in the proportion of proliferating germ cells after a 96-h exposure of seminiferous tubule cultures to metformin. In vivo, 6-week-old chickens treated with metformin for 3 weeks exhibited reduced testicular weight and a 50% decrease in testosterone levels. The expression of a marker of undifferentiated germ cells was unchanged in contrast to the decrease in expression of ‘protamine’, a marker of differentiated germ cells. In conclusion, these results suggest that metformin affects the testicular energy content and the proliferative ability of Sertoli and germ cells. Reproduction (2016) 151 527–538


2018 ◽  
Vol 9 (4) ◽  
pp. 373-376 ◽  
Author(s):  
G. G. Ribeiro ◽  
L. R. Pessôa ◽  
M. D. C. de Abreu ◽  
L. B. N. S. Corrêa ◽  
A. D’Avila Pereira ◽  
...  

AbstractThis study evaluated the effects of diet containing taro flour on hormone levels and the seminiferous tubules morphology of rats. After weaning, the male rats were divided into two groups (n=12 each): control group (CG) treated with control diet and taro group (TG), fed with 25% taro flour for 90 days. Food, caloric intake, mass and body length were evaluated at experiment end. Testis followed the standard histological processing. Immunostaining was performed using an anti-vimentin antibody to identify Sertoli cells. In histomorphometry, total diameter, total area, epithelial height, luminal height and luminal area were analyzed. The testosterone levels were performed using the radioimmunoassay method. Group TG presented (P<0.05): increase in mass, body length, testicular weight, histomorphometric parameters and hormonal levels. Food intake, calorie and Sertoli cells not presented statistical differences. The taro promoted increase in the testicles parameters and hormones.


2001 ◽  
Vol 86 (1) ◽  
pp. 413-421 ◽  
Author(s):  
Javier Regadera ◽  
Francisco MartÍnez-GarcÍa ◽  
Pilar González-Peramato ◽  
Alvaro Serrano ◽  
Manuel Nistal ◽  
...  

Androgen receptor (AR) immunohistochemistry was performed in an archival collection of adult human cryptorchid testes to determine whether AR cellular distribution and intensity of immunostaining were functions of the severity of cellular dysgenesis. The seminiferous tubule histology of cryptorchid testes collected from adults is marked by three specific patterns. 1) Seminiferous tubules are characterized as maintaining focal areas of germinal cell differentiation (albeit incomplete) that are interspersed with 2) tubules composed of Sertoli cells only, these latter cells being principally of the adult type, although dysgenetic and immature Sertoli cells may also be detected. 3) In contrast, there is a class of tubule that is characterized as being composed exclusively of Sertoli cells that are extremely dysgenetic in appearance. The majority of adult-type Sertoli cells found in the first types of tubules exhibited either robust or moderate AR staining intensity. Peritubular cells of these tubules also expressed a similar AR staining intensity. In contrast, in the more dysgenetic and immature type Sertoli cells found in the second type of tubules, the intensity of AR staining was significantly less, if not missing altogether. Finally, in the most dysgenetic tubules, Sertoli cell AR staining was never detected. To our knowledge, this is the first report in the literature that addresses the intensity of AR immunostaining in Sertoli cells of cryptorchid testes. The results presented herein are consistent with the interpretation that the intensity of AR staining in Sertoli cells diminishes as a function of the severity to which the cells are afflicted within a cryptorchid testis and that focal absence of AR expression in Sertoli cells correlates with a lack of local spermatogenesis in the tubules.


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