Immunoexpression of androgen receptors in testes of immature and mature stallions.
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Animals↗
Biomedical subjects
B Bilińska
Publications and source records attributed to B Bilińska.
Generation of the streaming potential by liposomes in cylindrical capillary. Experimental data.
A model of creation a streaming potential U as a result of colloidal particle movement in flow in a capillary has been described previously (Zawada 1996) as well as the systems for measurement (Zawada 1990, 1991). The filling of capillary with a solution of liposomes results in a labile adsorbance of liposomes on a capillary glass and changes the measured streaming potential. In order to minimalize these adverse effects, the capillary was covered with phospholipid layer of different composition. Some concentrations of stearylamine as a component of the phospholipid layer may fully compensate the surface charge of the glass capillary and can reduce the liposomes adsorption. The streaming potential of the liposomes solution depends on the ionic strength of the electrolyte and is smaller than the zeta potential for similar liposomes. This suggests that only a part of ions of the liposome ion atmosphere participate in creating of the streaming potential. These are the ions from the hydrodynamic slipping layer. The regression analysis of the relationships between streaming potential U and concentration of liposomes and next ionic strength of the electrolyte gave the value of the surface potential psi0 and the thickness of the hydrodynamic slipping layer d, that is independent of the ionic strength.
Amines↗
Immunohistochemical localization of androgen receptors in testicular cells of mice with mosaic mutation.
Mice with mosaic mutation could be one of the models of human Menkes disease, which is associated with abnormal cooper metabolism. The aim of the present study was to localize androgen receptors (ARs) in the testes by means of immunohistochemistry. AR expression was observed in the nuclei of all somatic cells such as Leydig cells, Sertoli cells, and peritubular cells in sections from testes of control and mosaic mutant males. In the latter, very strong immunoreactivity for AR as well as higher levels of steroid hormones in homogenates were noticed in comparison to control mice. No positive immunoreaction for ARs was seen in control sections incubated without the primary antibody.
Animals↗
Photoperiod-dependent capability of androgen aromatization and the role of estrogens in the bank vole testis visualized by means of immunohistochemistry.
Detection of steroid hormone receptors within a target tissue is important for an understanding of their crucial role in regulating of steroids' action. In the light of recent knowledge on the role of estrogens in male gonads the efforts were undertaken to clarify and discuss a role of androgen receptors, aromatase and estrogen receptors (ER) in mediating testosterone and/or estradiol action in testicular cells of bank voles that were kept under short or long light cycles. Immunohistochemistry was performed on paraplast embedded sections of the bank vole testes. First, androgen receptors were immunolocalized in testicular somatic cells while germ cell did not express any immunoreaction. Moreover, the ability to convert androgens to estrogens by various testicular cells was documented; aromatase immunoexpression was found in testis sections, not only in Leydig cells and Sertoli cells but also in germ cells. Finally, the expression of estrogen receptor-alpha (ERalpha) was observed in Leydig cells whereas the presence of estrogen receptor-beta (ERbeta) was detected in Sertoli and germ cells, namely spermatocytes and spermatids. The cellular distribution of androgen receptors appeared to be light -and age-dependent in adults; immunoexpression of aromatase and ERbeta was found to be both age -and photoperiod-dependent in germ cells.
Androgens↗
On the structure of human hair melanins from an infrared spectroscopy analysis of their interactions with Cu2+ ions.
Melanins were isolated from dark and red human hair and complexed with copper ions at various pH values in a complexing medium. IR spectra of melanins and their Cu2+-complexes for pellets with KBr were obtained. The IR spectra indicate that Cu2+ ions bound to melanins are fixed by different carboxyl and hydroxyl (phenolic and/or alcoholic) groups in the macromolecule. From these results it is concluded that, generally, melanin carboxyl groups are responsible for interactions of metal ions with the melanin molecule. Complexes of melanins isolated from dark and red human hair show structural differences when analysed by IR spectroscopy. Conclusions from these investigations assist in the differentiation of structures of analysed hair melanins. IR spectral analysis of melanin samples and their complexes suggest that melanin samples obtained from red hair may contain eumelanin.
Copper↗
Immunofluorescent localization of the StAR protein in mitochondria of mouse Leydig cells in vitro.
The Steroidogenic Acute Regulatory (StAR) protein is assumed to enhance the rate-limiting step of the steroid biosynthesis. Now, it is the most likely candidate, responsible for acutely regulating transfer of cholesterol from the outer to the inner mitochondrial membrane. In this study, the immunoreactive StAR protein was observed in the mitochondria of mouse cultured Leydig cells stimulated by hCG andtesticular macrophage-conditioned medium. Immunocytochemistry was performed using a polyclonal rabbit antibody against the StAR protein. For selective staining of mitochondria in Leydig cells, the Mito Tracker dye was used. Computerized, superimposed images from double-fluorescence staining showed a remarkable degree of similarity in the distribution of the StAR protein and mitochondria, indicating mitochondrial localization of StAR.
Animals↗
Localization of alpha-tubulin in the rat cumulus oophorus before and during preovulatory expansion.
Distribution of alpha-tubulin was investigated in the cumulus oophorus complexes (COCs) of the rat using anti-alpha-tubulin monoclonal antibody and fluorescence microscopy. Localization of alpha-tubulin was assessed in the compact and fully expanded COCs isolated directly from the preovulatory follicles and in the cryosections containing these structures. In the cryosections containing COCs, the submembranous distribution of alpha-tubulin marked the characteristic cell shapes and showed the lack of cell projections. In the freshly isolated COCs three-dimensional cellular arrangement was visible showing that the dispersed cells formed almost no projections and were not interconnected. The use of a higher magnification revealed a dense microtubular network radiating from centrosomes and extending to the plasma membrane. This network showed discontinuous distribution of submembranous alpha-tubulin in some of these cells. The latter change could be attributed to the increased progesterone production.
Animals↗
Immunolocalization and activity of aromatase in the bank vole testes.
A direct approach to identify the cellular source of P450 aromatase in the bank vole testes (seasonally breeding rodents) is the use of immunohistochemistry with a specific antibody that recognizes this enzyme. To confirm the presence of functional aromatase, its activity was measured in microsomal preparations of whole testes and of seminiferous tubules by means of biochemical assay with tritiated androstenedione. The assay was validated using increasing concentrations of both microsomal preparations. Immunoreactive aromatase was found in Leydig cells, Sertoli cells, and germ cells, especially in spermatocytes and spermatids. The aromatase activity was present in microsomal fractions of whole testis and seminiferous tubules. The immunolocalization of P450 aromatase and aromatase activity have been found as photoperiod-dependent.
Animals↗
The site of aromatization in the mouse cryptorchid testis.
Using the mouse cryptorchid model, degenerations of germ cells were observed as well as a reduced size of seminiferous tubules, while the area of the interstitial tissue increased. Aromatase, the enzyme responsible for the conversion of androgens into oestrogens, was immunolocalized in Leydig cells and in germ cells from both scrotal and abdominal testes, and in Sertoli cells only in a control testis. In the cryptorchid testis, aromatase was strongly expressed in a few tubules, including those spermatids that were still present. Other cells inside the tubules were negative for aromatase. In both testes, oestrogen receptors alpha were expressed only in Leydig cells. Strong aromatase expression in germ cells indicates an additional source of oestrogens in the testis besides the interstitial tissue.
Animals↗
Cytochrome P450 aromatase in the testis of immature and mature pigs.
Aromatization of androgens into estrogens is performed by a microsomal enzyme, the cytochrome P450 aromatase. A direct approach for identifying the cellular source of aromatase is the use of immunohistochemistry with a specific antibody that recognizes aromatase. The pig presents some unusual features with regard to the synthesis of testosterone and estrogens in the male gonads. In testes from prepubertal males, testosterone level measured radioimmunologically, was lower than in testes from adult pig, while estrogen secretion was relatively high and comparable to that of mature porcine gonads. Immunolocalization of aromatase in testes from both immature and mature pigs was confined to the Leydig cell cytoplasm. The intensity of immunohistochemical staining indicated the presence of unsynchronous Leydig cell population. Other somatic cells and germ cells were negative for aromatase. In control tissue sections, incubated in the absence of the primary antibody or in the presence of normal rabbit serum, no positive staining was observed. Western blot analysis revealed one major band of aromatase about 50-52 kDa in testes from both immature and mature pigs.
Aging↗
Localization of cytochrome P450 aromatase and estrogen receptors alpha and beta in testicular cells--an immunohistochemical study of the bank vole.
Age- and light-dark cycle-induced changes in immunoexpression of aromatase and estrogen receptors alpha and beta were studied in testes of a seasonally breeding rodent, the bank vole. Seasonal breeding can be mimicked by exposure to different light cycle regimes. In testes of animals that were exposed to long light cycles of 18 h light and 6 h darkness aromatase was in Leydig cells and seminiferous tubules, mainly in spermatocytes, whereas in animals exposed to short light cycles (6 h light and 18 h darkness), only Leydig cells exhibited positive immunostaining for aromatase. Whatever the age of animals, immunostaining for estrogen receptor alpha was restricted to Leydig cells, whereas estrogen receptor beta immunoreactivity was mainly confined to Sertoli cells of both of immature and adult animals, independently of the regimes of light. Additionally, in testes of animals that were exposed to long light cycles, estrogen receptor beta immunoreactivity was observed in seminiferous tubules. Nuclei of germ cells, predominantly spermatocytes and elongated spermatids, were strongly positive which correlated well with aromatase immunoreactivity. As far as we know, the present study is the first study that describes immunoexpression of aromatase and both estrogen receptors alpha and beta in testis of the bank vole. We provide strong evidence that estrogens are not only produced in Leydig cells but also in germ cells in this rodent. These female hormones may play a physiological role in testis, likely in the development of germ cells during spermatogenesis.
Aging↗
Number of chromocentres in the nuclei of mouse Sertoli cells in relation to the strain and age of males from puberty to senescence.
Nuclei of mouse Sertoli cells were examined on air-dried toluidine blue-stained preparations to analyse factors influencing the aggregation of heterochromatin into chromocentres. For the CBA strain males tested at 1.3, 2, 3, 6, 9 and 12 months of age, mean numbers of heterochromatin bodies were 4.8, 2.4, 2.1, 1.8, 1.6 and 1. 4, respectively; two chromocentres predominated from 2 to 9 months of age. In the KE strain, heterochromatin aggregation was significantly accelerated; nuclei containing only one chromocentre were predominant from 6 months. The number of chromocentres did not change with the stages of the seminiferous cycle, and after 1 month of cryptorchid condition. Cryptorchidism resulted in disruption of spermatogenesis and Sertoli cell dysfunction, as demonstrated by the lack of immunohistochemically detectable androgen receptors. The difference in the number of chromocentres between KE and CBA Sertoli cells persisted after 3 days of in vitro culture, but unidentified cells with numerous chromatin bodies were also observed. Testing recombinant inbred strains indicates that at least two genes are involved in the difference in the number of chromocentres between progenitor KE and CBA strains; however, no correlations were found with 15 marker loci or with parameters linked to reproduction. Of the eight strains tested, AKR and C3H showed a 'CBA-like' chromocentre pattern; C57BL, B10.BR, B10.BR-Y(del) and KP were 'KE-like'; and BALB/c and DBA/2 were intermediate. The results showed that centromere aggregation in the Sertoli cell progresses throughout the life of a male in a strain specific manner; however, its functional significance remains unknown.
Aging↗
Correlation between NADPH-diaphorase and iNOS in bank vole Leydig cells in vitro and in testicular sections with the use of histochemistry and immunocytochemistry.
Histochemistry for NADPH-diaphorase detects an enzymatic activity associated with nitric oxide synthase while immunohistochemistry detects the nitric oxide synthase molecule. NADPH-diaphorase and inducible isoform of nitric oxide synthase in Leydig cells in vitro and in testis sections of the bank vole were demonstrated histochemically and immunocytochemically. Histochemical studies revealed localization of NADPH-diaphorase reaction product in the cytoplasm of cultured Leydig cells as well as in the interstitial area, mainly in Leydig cells and in vascular endothelium. Distribution pattern of NADPH-diaphorase was different in Leydig cell cytoplasm of individual cells. Using immunocytochemistry, the immunoreactivity for nitric oxide synthase was observed both in cultured Leydig cells and testis sections. Moreover, a co-localization of positively immunostained cells with those histochemically detected was noticed. Addition of hCG to the cultured medium or injections in vivo resulted in a small decrease in reaction intensity in Leydig cells. Treatment with N omega-nitro-L-arginine methyl ester resulted in distinctly weaker reactivity of the enzymes studied which was correlated with a higher testosterone and estradiol levels in Leydig cells measured radioimmunologically. The results have indicated that nitric oxide synthase is able to act directly within the male gonad regulating androgen secretion by Leydig cells.
Animals↗
Immunohistochemical localization of estrogen receptors in the ovine corpus luteum throughout the estrous cycle.
Using immunohistochemistry and Western blot analysis we attempted to identify the estrogen receptors in ovine luteal cells at different stages of the estrous cycle. Monoclonal antibody against estrogen receptors was used for immunolocalization of estrogen receptor-alpha in corpora lutea sections. Generally, the most intense cytoplasm staining was present in large luteal cells. On the 6th day of the estrous cycle, weak immunostaining of estrogen receptors was observed in large luteal cells as well as in the connective tissue. Luteal cells from regressing corpora lutea expressed the weakest immunostaining. The most intense immunoreactivity for estrogen receptors was found in sections of corpora lutea collected on the 9th day of the cycle. Both, cytoplasmic and nuclear localization was observed depending on cell types in the ovine corpus luteum. Our studies demonstrated the presence of the estrogen receptor-alpha in the luteal cells and suggested an autocrine/paracrine role of estrogen in the regulation of estrous cycle in sheep.
Animals↗
Immunolocalization of androgen receptors in testicular cells of prepubertal and pubertal pigs.
In the testis, androgen receptors are known to mediate autocrine and paracrine effects of androgens on Leydig cell function and spermatogenesis. The pig presents some unusual features with regard to the synthesis of testosterone and estrogens in the male gonads. In testes from prepubertal males, testosterone level was lower than in testes from adult boars, while estrogen secretion was relatively high and comparable to that of mature porcine gonad. Immunolocalization of androgen receptors and intensity of immunohistochemical staining was age-dependent. In testis sections from adult boars, androgen receptors were found in nuclei of all somatic cells such as Leydig cells, Sertoli cells, and peritubular-myoid cells, whereas in sections from immature pigs only in the Leydig cell cytoplasm showed positive immunoreaction for androgen receptors. In control tissue sections incubated with omission of the primary antibody, no positive staining was observed. Detection of the androgen receptors in testicular cells of the pig is important for understanding of their central role in mediating androgen action.
Aging↗
Immunolocalization of androgen receptors in testicular cells during postnatal development of the bank vole (Clethrionomys glareolus, S.).
Determination of the cellular distribution of the androgen receptors within the testis is of great importance for an understanding of their essential role in mediating of androgen action in the male gonad. In bank voles, which are seasonally breeding rodents, photoperiod is one of the most important factors inducing profound changes in the morphology and hormonal activity of the testes. Immunolocalization of androgen receptors was found in all somatic cells such as Sertoli cells, Leydig cells, and peritubular-myoid cells, however, distribution of the androgen receptors in various cell types depended on age of animals. Intensity of immunoreactivity was noticed as age and photoperiod-dependent. Males reared under different light regimes showed a significant correlation between the length of light and sexual maturation. Therefore, morphology of the testis from young and adult bank voles was also presented.
Age Factors↗
The effect of testicular macrophages, macrophage-conditioned medium and interleukin-1alpha on bank vole Leydig cell steroidogenesis.
It has already been accepted that the function and activity of the testis is regulated not only by gonadotrophins, but also by many locally produced factors and by cell-cell interactions. That is why the aim of our work was to determine whether macrophages and/or their products have an influence on Leydig cell steroidogenic activity. The source of Leydig cells and macrophages were male bank voles of spring and autumn generations, reared in 18 light:6 dark or 6 light:18 dark (18L:6D or 6L:18D) conditions for 7-8 weeks. The Leydig cells were growing in monocultures or in co-cultures with macrophages (testicular or peritoneal), either as control or hCG-stimulated ones. To some of the cultures 6 IU/ml of interleukin 1alpha (IL-1alpha) was added. After then the cells were analysed morphologically, histochemically, and radioimmunologically. In the present study we found many differences in morphology and steroidogenic activity of Leydig cells obtained from different photoperiods. Leydig cells from a long day formed monolayer contrary to the cells from a short one growing as single cells or in clusters. Moreover, Leydig cells from a long photoperiod produced more testosterone and were sensitive to the stimulatory effect of both testicular macrophages and testicular macrophage-conditioned medium. They were also more sensitive to the inhibitory influence of IL-1alpha.
Androgens↗
The effect of testicular macrophages, macrophage-conditioned medium and interleukin-1alpha on the cytoskeleton of bank vole Leydig cells.
Recently, morphological and functional interactions between cytoskeletal elements and their involvement in cell movements, shape changes and/or translocation of organelles have been intensively studied. Thus, the aim of our work was to determine whether testicular macrophages and/or their products have an influence on Leydig cell cytoskeleton. The source of Leydig cells and macrophages were male bank voles from spring and autumn generations, reared in different regime of light for 7-8 weeks. The Leydig cells were growing in monocultures or in co-cultures with testicular macrophages. All cell cultures were divided to controls or human chorionic gonadotropin-stimulated ones. To some of the cultures testicular macrophage-conditioned medium or interleukin-1alpha were added. The cells were analysed immunocytochemically and radioimmunologically. In Leydig cells obtained from animals kept in a long day, grown in co-cultures with macrophages as well as in those stimulated by testicular macrophage-conditioned medium, distinct rearrangements of microtubules and microfilaments were observed. This phenomenon was strengthened in the presence of hCG in culture media. Concomitantly, basal and hCG-stimulated level of testosterone was enhanced, which indicates the possible involvement of the cytoskeleton in the process of androgen biosynthesis. The influence of IL-1alpha on reorganization of cytoskeletal structures was not observed, suggesting that in the modulation of steroidogenesis by this cytokine cytoskeletal elements do not play an important role.
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