Amount Of Smooth Endoplasmic Reticulum Research Articles

Physiological and developmental dysfunctions in the dengue vector Culex pipiens (Diptera: Culicidae) immature stages following treatment with zinc oxide nanoparticles

The medical value of mosquitoes attracted researchers worldwide to search for a valuable way to control such serious insects. The continuous development of resistance against chemical insecticides pushed toward looking for novel and promising compounds against mosquitoes. In this study, the toxicity and physio-developmental effects of 10–30 nm spherical zinc oxide nanoparticles (ZnONPs) in aqueous suspension was addressed against the first larval instar of Culex pipiens mosquito. The calculated value of LC50 was about 0.892 g/L while the sub lethal concentration LC20 recorded about 0.246 g/L. Larvae treated with ZnONPs suffered reduced growth rate, longer developmental period and malformations in the breathing tube. Furthermore, the treated larvae showed clear abnormal appearance of the gastric caeca and midgut epithelia under transmission electron microscope (TEM). These abnormalities appeared as condensation of the nuclear chromatin, abnormal shape or absence of microvilli, highly increased amount of smooth endoplasmic reticulum in the cytoplasm and appearance of numerous vacuoles. Additionally, ZnONPs interfered with several biochemical pathways such as induction of oxidative stress which appeared in the form of increased levels of hydrogen peroxide and inability to activate the detoxifying enzymes alkaline phosphatase (ALP), catalase and glutathione peroxidase (GPX). On the contrary, the activity of the antioxidant enzyme superoxide dismutase (SOD) increased in treated larvae. Furthermore, LC20 and LC50 of ZnONPs inhibited the growth rate of the larval gut fauna in vitro. These results clearly show that ZnONPs target several tissues leading to serious alteration in the physiological and developmental processes in C. pipiens mosquito larvae.

Cytoarchitectural improvement in Leydig cells of diabetic rats after treatment with aqueous and ethanol extracts of Dracaena arborea (Dracaenaceae)

Background and aimRecent studies have demonstrated the androgenic effects of Dracaena arborea in castrated and diabetic rats, but the cytoarchitectural mechanism at the level of Leydig cells (LCs) justifying this improvement in androgens production in diabetic rats has never been examined. We investigated the effects of aqueous and ethanol extracts of D. arborea on diabetes-induced cytoarchitectural impairments of LCs in rats. Experimental procedureBesides a normal group, 4 groups of diabetic rats were treated orally with Millipore water (10 ml/kg, diabetic), sildenafil citrate (1.44 mg/kg), aqueous (500 mg/kg) and ethanol (100 mg/kg) extracts of D. arborea for 21 days. On day 22, rats were sacrificed and the testes were removed and prepared for electron microscopic analyses of LCs ultrastructure. Results and conclusionThe ultrastructure of LCs in control rats was normal, while that in diabetic rats exhibited large heterochromatization in the nuclei, reduced amount of smooth endoplasmic reticulum with no lipid droplets in the cytoplasm, many autophagosomes and degenerated mitochondria containing lots of electron dense granules in the matrix. Interestingly, treatment with D. arborea especially its aqueous extract (500 mg/kg) alleviated these impairments, characterized by a rarification of heterochromatization in the nuclei coupled to an increase and the presence in the cytoplasm of prominent smooth endoplasmic reticulum and a reduction of electron dense granules in the matrix of mitochondria. These alleviating properties of D. arborea on LCs ultrastructure of diabetic rats could explain its androgenic potential. These results are useful for the management of patients suffering from diabetes-induced hypogonadism.

Prophylactic role of β-carotene against acrylonitrile-induced testicular toxicity in rats: Physiological and microscopical studies

Acrylonitrile (ACN) is an aliphatic nitrile product which is extensively used in various synthetic chemical industries. ACN is known to exert toxic actions to human beings as well as experimental animals. The present study was designed to examine the ability of β-carotene, a naturally occurring antioxidant, to attenuate ACN-induced testicular toxicity in adult albino rats. Daily oral administration of ACN at a dose level of 30mg/kg b.w. (7.2mg/animal) to male rats for a period of 5 days significantly reduced the levels of serum testosterone (T), androsterone, follicle-stimulating hormone (FSH) and luteinizing hormone (LH) which indicate injury to the testis function. Also, it decreased serum and testicular glutathione (GSH) content and glutathione-S-transferase (GST) activity. While, ACN induced lipid peroxidation as indicated by markedly increased malondialdehyde (MDA). ACN intoxication also induced marked alterations in most of the seminiferous tubules including germ cell depletion, tubular atrophy, maturation arrest, complete necrosis as well as multinucleated giant cell formation. Expansion of intertubular spaces and interstitial haemorrhage were also illustrated. Ultrastructural examination of the seminiferous tubules revealed thickened boundary tissue, pyknosis of Sertoli cell nuclei, damaged mitochondria and smooth endoplasmic reticulum-derived vacuoles. Spermatogenic cells also demonstrated altered cytoplasmic organelles, vacuoles of varying sizes and deformed spermatids. Mitochondrial disruption and a decrease in the amount of smooth endoplasmic reticulum were observed in Leydig cells. Compared to ACN-treated animals, pretreatment with β-carotene and its co-administration with ACN once daily at a dose of 40mg/kg b.w. (9.6mg/animal) for 30 days induced a remarkable degree of improvement in the levels of endocrine parameters including T, androsterone, FSH and LH. Also, it mitigates serum and testicular GSH content, GST activity and MDA level. Moreover, it protects testicular tissues and cell structures.In conclusion, the present results clearly demonstrate the prophylactic role of β-carotene against ACN-induced testicular toxicity in rats.

Cells producing insulin-like androgenic gland hormone of the giant freshwater prawn, Macrobrachium rosenbergii, proliferate following bilateral eyestalk-ablation

We found that the androgenic gland (AG) of Macrobrachium rosenbergii possesses three cell types. Type I cells are small polygonal shaped-cells (13.4 μm in diameter), stain strongly with hematoxylin–eosin (H&E), have abundant multilayered rough endoplasmic reticulum (rER), and nuclei containing mostly heterochromatin. Type II cells are slightly larger (18.6 μm in diameter), stain lightly with H&E, have rER with dilated cisternae, and nuclei containing mostly euchromatin. Type III cells (previously undescribed) are similar in size and shape to type I cells, but the cytoplasm is unstained and they have a high amount of smooth endoplasmic reticulum (sER) and mitochondria with tubular cristae. Bilateral eyestalk-ablation resulted in AG hypertrophy with a proliferation and predominance of type I cells as determined by bromodeoxyuridine (BrdU) assays. Expression of insulin-like androgenic gland hormone (Mr-IAG), determined by immunohistochemistry, was weak in type I cells, strong in type II cells of both the intact and eyestalk-ablated, and negative in type III cells. It was also detected in spermatogonia, nurse cells, and epithelium lining of the spermatic duct. The function of Mr-IAG in these tissues is yet to be elucidated but the distribution implies a strong role in male reproduction.

267 ULTRASTRUCTURAL CHARACTERISTICS OF NON-MATURED AND IN VITRO MATURED OOCYTES COLLECTED FROM FOLLICULAR, LUTEAL, AND INACTIVE OVARIES OF DOMESTIC CAT (FELIS CATUS) DURING BREEDING AND NON-BREEDING SEASON

The aim of this experiment was to describe the ultrastructural characteristics of non-matured (NM) and in vitro matured (IVM) cumulus–oophorus complexes (COC) recovered from adult queens during the breeding season (BS; July, August, and September) and the non-breeding season (NBS; January, February, and March) in southeast Brazil. Transmission electronic microscopy was performed in NM COC immediately after harvest, and IVM COC were matured for 36 h before transmission electronic microscopy. All IVM COC during both seasons were at metaphase II stage. Specimens were divided into COC from inactive ovaries, follicular ovaries, and luteal ovaries recovered during BS and NBS. During NBS, NM follicular and inactive COC presented a narrow perivitelline space covered with microvilli, which were less evident in NM luteal COC. Cumulus-cell projections penetrated the zona pellucida forming gap junctions with the oolemma in all NM COC. In the cytoplasm of NM inactive COC, lipid droplets and vesicles were evenly distributed in the ooplasm except for in the cortical zone, where clusters of mitochondria were observed. Non-matured luteal COC were also characterised by peripheral mitochondrial clusters, but greater clusters could also be seen centrally in the cytoplasm. In contrast, NM follicular COC were characterised by evenly distributed mitochondria within the ooplasma. In NM inactive and follicular COC, cortical granules were seen only in the central region of the cytoplasm, but the electron density of these organelles appeared to be low and Golgi complexes were often seen in association with these granules. The density of cortical granules in NM follicular COC was higher, but they were also present in central regions of the ooplasm. In all NM COC, a well-developed Golgi complex was observed. In all IVM COC, mitochondria clusters were no longer observed, and these organelles presented an even distribution toward the ooplasm. High-density cortical granules were present in the peripheral region of all IVM COC, although a small number could still be observed in central region of the ooplasm of IVM follicular COC. The perivitelline space was more prominent in IVM COC. During BS, COC characteristics were similar to NM COC during NBS; the presence of mitochondrial clusters associated with lipid droplets, well-developed cortical granules, and the presence of nuage could be observed, except that all cortical granules located in the central region of the cytoplasm of NM follicular COC during BS. A great amount of smooth endoplasmic reticulum could be verified in NM follicular and luteal COC. During BS, all IVM COC presented uniform distribution of mitochondria and peripheral distribution of cortical granules in the ooplasma. These results indicate that IVM was efficient in inducing the morphological changes necessary for cytoplasmic maturation of cat COC, independently of the ovarian status. The authors acknowledge FAPESP.

Increased Exposure to Estrogens Disturbs Maturation, Steroidogenesis, and Cholesterol Homeostasis via Estrogen Receptor α in Adult Mouse Leydig Cells

Deteriorated male reproductive health has been connected to overexposure to estrogens or to imbalanced androgen-estrogen ratio. Transgenic male mice expressing human aromatase (AROM(+) mice) serve as an apt model for the study of the consequences of an altered androgen-estrogen ratio. Our previous studies with AROM(+) mice showed that low androgen levels together with high estrogen levels result in cryptorchidism and infertility. In the present study, the AROM(+) mice were shown to have severe abnormalities in the structure and function of Leydig cells before the appearance of spermatogenic failure. Decreased expression of adult-type Leydig cell markers (Ptgds, Vcam1, Insl3, Klk21, -24 and -27, Star, Cyp17a1, and Hsd17b3) indicated an immature developmental stage of the Leydig cells, which appears to be the first estrogen-dependent alteration. Genes involved in steroidogenesis (Star, Cyp17a1, and Hsd17b3) were suppressed despite normal LH levels. The low expression level of kallikreins 21, 24, and 27 potentially further inhibited Leydig cell function via remodeling extracellular matrix composition. In connection with disrupted steroidogenesis, Leydig cells showed enlarged mitochondria, a reduced amount of smooth endoplasmic reticulum, and an accumulation of cholesterol and precursors for cholesterol synthesis. The results of studies with AROM(+) mice crossed with estrogen receptor alpha or beta (ERalpha and ERbeta, respectively) knockout mice lead to the conclusion that the structural and functional disorders caused by estrogen exposure were mediated via ERalpha, whereas ERbeta was not involved.

Developmental changes in localization of steroid synthesis enzymes in camelid placenta

The uninucleate trophoblast of epitheliochorial camelid placenta produces multinucleate giant cells starting between day 30 and day 35 of pregnancy. The giant cells are found scattered along the trophoblast at similar frequency throughout gestation. Light microscope immunocytochemistry indicates that the four steroid synthesis enzymes (cholesterol side chain cleavage, 3beta-hydroxysteroid de-hydrogenase, 17alpha-hydroxylase and aromatase) are present in all uninucleate trophoblast cells between day 14 and day 30 of pregnancy, but are found only in the giant cells once they are established, and that this localization persists until term. The giant cells show massive amounts of smooth endoplasmic reticulum and numerous small mitochondria, again as has been shown in other steroid-producing cells. As progesterone from the corpus luteum is necessary throughout gestation in camels, the capacity for oestrogen production by the trophoblast presumably has an important role, but one limited mostly to the immediate vicinity of the fetomaternal interface.

Developmental changes in localization of steroid synthesis enzymes in camelid placenta.

The uninucleate trophoblast of epitheliochorial camelid placenta produces multinucleate giant cells starting between day 30 and day 35 of pregnancy. The giant cells are found scattered along the trophoblast at similar frequency throughout gestation. Light microscope immunocytochemistry indicates that the four steroid synthesis enzymes (cholesterol side chain cleavage, 3beta-hydroxysteroid de-hydrogenase, 17alpha-hydroxylase and aromatase) are present in all uninucleate trophoblast cells between day 14 and day 30 of pregnancy, but are found only in the giant cells once they are established, and that this localization persists until term. The giant cells show massive amounts of smooth endoplasmic reticulum and numerous small mitochondria, again as has been shown in other steroid-producing cells. As progesterone from the corpus luteum is necessary throughout gestation in camels, the capacity for oestrogen production by the trophoblast presumably has an important role, but one limited mostly to the immediate vicinity of the fetomaternal interface.

Recent progress in the neurobiology of the vomeronasal organ.

In many terrestrial tetrapodes, a pair of vomeronasal organs (VNOs), which are chemosensory apparatuses, are situated at the base of the nasal septum in the anterior nasal cavity. The purposes of this review are to summarize comparative neuroanatomy and to introduce recent progress in neurobiological studies of the VNO. Five types of VNOs can be identifiable in terms of anatomical organization; snakes possess the most complex one. Sensory cells in the VNO, vomeronasal receptor neurons (VRNs), are located in its neuroepithelium, vomeronassal sensory epithelium. The VRNs retain the characteristic of epithelial cells in that they are born continuously from progenitor cells. They contain two prominent subcellular structures: microvilli and extraordinarily large amounts of smooth endoplasmic reticulum and a few unique glycoconjugates. The VRNs express two types of G-protein -subunits: Gi(alpha2) and Go(alpha) and each of them is coupled with putative pheromone receptors, V1Rs and V2Rs, respectively. Recent physiological and biochemical studies have demonstrated that pheromones depolarize the V1R-Gi(alpha2) and V2R-Go(alpha) VRNs via IP(3)-mediated mechanisms. The VRNs do not show adaptation and are ultrasensitive to putative pheromones. Other than being a chemosensory organ, the VNO and its primordium might play important roles for brain development; hypothalamic neurons that produce gonadotropin-releasing hormone are born in the VNO primordium and a few other neuron-like cells may be born in the VNO primordium and VNO. In human fetuses, anatomical findings strongly suggest that their VNOs contain a neuroepithelium. By contrast, it is unlikely that adult human VNO serves as a chemosensory organ.

Olfactory mucosa ultrastructure in the short-tailed shrews, Blarina brevicauda and Blarina carolinensis.

The olfactory mucosae of the northern short-tailed shrew, Blarina brevicauda, and the southern short-tailed shrew, Blarina carolinensis, were examined by light and electron microscopy. A well-developed olfactory epithelium was observed that included all of the cells necessary to provide for a sensitive olfactory system, suggesting that olfaction plays a major role in the behavior of these animals. There were no significant differences between the olfactory mucosae of these two species. The general features of the olfactory epithelium in these shrews were similar to those reported for several other macrosmatic mammals. A new type of supporting cell, called the light supporting cell, was observed in these shrews. The light supporting cell cytoplasm exhibited very little staining by light microscopy and had low electron density by transmission electron microscopy compared to that of the more common dark supporting cell. The light supporting cell had a convex apical surface with microvilli and lacked the large amounts of smooth endoplasmic reticulum (SER) typical of the apical cytoplasm of the dark supporting cell. In the lamina propria of the mucosa, the Bowman's glands consisted of two cell types, one with electron-lucent, alcian blue-positive granules, and the other with electron-dense PAS-positive granules. The cell with electron-lucent granules contained large amounts of SER and small clumps of rough ER. The cells with electron-dense granules had large amounts of RER and little SER.

Efficiency of spermatogenesis: a comparative approach

Efficiency of spermatogenesis is the estimated number of spermatozoa produced per day per gram of testicular parenchyma. Spermatogenesis is the process of cell division and cell differentiation by which spermatozoa are produced in testes. Efficiency of spermatogenesis is influenced by species differences in the numerical density of germ cell nuclei and in the life span of these cells. Activities of spermatogonia, spermatocytes, and spermatids partition spermatogenesis into three major divisions (spermatocytogenesis, meiosis, and spermiogenesis, respectively). Spermatocytogenesis involves mitotic germ cell division to produce stem cells and primary spermatocytes. Meiosis involves duplication of chromosomes, exchange of genetic material, and two cell divisions that reduce the chromosome number and yield four spermatids. In spermiogenesis, spherical spermatids differentiate into mature spermatids which are released in the lumen of seminiferous tubules as spermatozoa. Spermatogenesis and germ cell degeneration can be quantified from numbers of germ cells in various developmental steps throughout spermatogenesis. Germ cell degeneration occurs throughout spermatogenesis; however, the greatest impact occurs during spermatocytogenesis and meiosis. There are species and seasonal influences on the developmental steps in spermatogenesis at which germ cell degeneration occurs. Number of Sertoli cells, amount of smooth endoplasmic reticulum of Leydig cells, and the number of missing generations of germ cells within the spermatogenic stage of the cycle influence efficiency of spermatogenesis. Efficiency of spermatogenesis is influenced to the amount of germ cell degeneration, pubertal development, season of the year, and aging of humans and animals.

Comparative ultrastructure of Clara cells in neonatal and older cattle

ABSTRACT Calf lungs were fixed with glutaraldehyde and examined by scanning (SEM) and transmission (TEM) electron microscopy to compare the ultrastructure of Clara cells in terminal bronchioles of neonatal calves and older cattle. In the neonatal calf, SEM revealed numerous smooth-surfaced Clara cells protruding above a similar number of ciliated cells, whereas in older animals the surface of Clara cells was lobulated. Thin sections examined by TEM revealed numerous cuboidal to columnar Clara cells with indented nuclei and a pale cytoplasm filled with faintly granular glycogen in the neonatal calf. Some cells were characterized by apical dense and/or pale membrane-bound granules or secretory droplets. Many cells had an apical tubular network of cisternae that were partly smooth and partly decorated with ribosomes. Ultrastructural comparison of Clara cells in a 2-day-old calf with those of 14- and 19-day-old, 4- and 5.5-month-old, and 3.5-year-old cattle revealed a striking reduction in the amount of glycogen per cell after 14 days. The number of cells with apical granules was small at all ages, and the density of the secretory granules varied greatly in different cells. A variable amount of smooth endoplasmic reticulum (SER) was present but was less prominent than cisternae of ribosomal endoplasmic reticulum (RER). In older cattle, the limited amount of SER compared to the RER and secretory granules suggests that bovine Clara cells are more likely to be secretory than detoxifying. J. Morphol. 244:143–151, 2000. © 2000 Wiley-Liss, Inc.

Fine structure and development of the cuticle of Intoshia variabili (Orthonectida)

The body of free‐swiming mature Intoshia variabili (Orthonectida) is covered by a thin cuticle, 0.3 μm thick. The cuticle is formed at the time when the orthonectid embryos develop in the plasmodium. The process of cuticle formation begins just after the first cilia begin to appear at the surface of the ciliated cells. At first, small extensions of the cell membrane appear at the surface of the cell, more or less parallel to the cell surface. As they develop futher, they stand up, and amorphic material begins to appear between them. The extensions then become microvilli and obtain their final shape, with a small subdistal swelling and a narrower distal part. They are situated very regularly on the surface of the cell. After the microvilli have obtained their final form, material between them begins to get its final structure typical of the adult form. During the period when the mature orthonectid begins to leave the plasmodium and emerge from the host, the regular microvilli begin to disappear, and only small irregular extensions are present under the cuticle on the surface of the cell. During the process of cuticle formation a large amount of smooth endoplasmic reticulum develops in the cells, but once the cuticle is formed it gradually disappears.

Factors affecting spermatogenesis in the stallion

Spermatogenesis is a process of division and differentiation by which spermatozoa are produced in seminiferous tubules. Seminiferous tubules are composed of somatic cells (myoid cells and Sertoli cells) and germ cells (spermatogonia, spermatocytes, and spermatids). Activities of these three germ cells divide spermatogenesis into spermatocytogenesis, meiosis, and spermiogenesis, respectively. Spermatocytogenesis involves mitotic cell division to increase the yield of spermatogenesis and to produce stem cells and primary spermatocytes. Meiosis involves duplication and exchange of genetic material and two cell divisions that reduce the chromosome number to haploid and yield four spermatids. Spermiogenesis is the differentiation without division of spherical spermatids into mature spermatids which are released from the luminal free surface as spermatozoa. The spermatogenic cycle (12.2 days in the horse) is superimposed on the three major divisions of spermatogenesis which takes 57 days. Spermatogenesis and germ cell degeneration can be quantified from numbers of germ cells in various steps of development throughout spermatogenesis, and quantitative measures are related to number of spermatozoa in the ejaculate. Germ cell degeneration occurs throughout spermatogenesis; however, the greatest seasonal impact on horses occurs during spermatocytogenesis. Daily spermatozoan production is related to the amount of germ cell degeneration, pubertal development, season of the year, and aging. Number of Sertoli cells and amount of smooth endoplasmic reticulum of Leydig cells and Leydig cell number are related to spermatozoan production. Seminiferous epithelium is sensitive to elevated temperature, dietary deficiencies, androgenic drugs (anabolic steroids), metals (cadmium and lead), x-ray exposure, dioxin, alcohol, and infectious diseases. However, these different factors may elicit the same temporary or permanent response in that degenerating germ cells become more common, multinucleate giant germ cells form by coalescence of spermatocytes or spermatids, the ratio of germ cells to Sertoli cells is reduced, and spermatozoan production is adversely affected. In short, spermatogenesis involves both mitotic and meiotic cell divisions and an unsurpassed example of cell differentiation in the production of the spermatozoon. Several extrinsic factors can influence spermatogenesis to cause a similar degenerative response of the seminiferous epithelium and reduce fertility of stallions.

Three-Dimensional Organization of Smooth Endoplasmic Reticulum in Hippocampal CA1 Dendrites and Dendritic Spines of the Immature and Mature Rat

Recent studies have shown high levels of calcium in activated dendritic spines, where the smooth endoplasmic reticulum (SER) is likely to be important for regulating calcium. Here, the dimensions and organization of the SER in hippocampal spines and dendrites were measured through serial electron microscopy and three-dimensional analysis. SER of some form was found in 58% of the immature spines and in 48% of the adult spines. Less than 50% of the small spines at either age contained SER, suggesting that other mechanisms, such as cytoplasmic buffers, regulate ion fluxes within their small volumes. In contrast, >80% of the large mushroom spines of the adult had a spine apparatus, an organelle containing stacks of SER and dense-staining plates. Reconstructed SER occupied 0.001-0.022 microm3, which was only 2-3.5% of the total spine volume; however, the convoluted SER membranes had surface areas of 0.12-2.19 microm2, which were 12 to 40% of the spine surface area. Coated vesicles and multivesicular bodies occurred in some spines, suggesting local endocytotic activity. Smooth vesicles and tubules of SER were found in continuity with the spine plasma membrane and margins of the postsynaptic density (PSD), respectively, suggesting a role for the SER in the addition and recycling of spine membranes and synapses. The amount of SER in the parent dendrites was proportional to the number of spines and synapses originating along their lengths. These measurements support the hypothesis that the SER regulates the ionic and structural milieu of some, but not all, hippocampal dendritic spines.

Efficiency of spermatogenesis.

Spermatogenesis is a process of division and differentiation by which spermatozoa are produced in seminiferous tubules. A measure of efficiency of spermatogenesis is the estimated number of spermatozoa produced per day per gram of testicular parenchyma. This measure is not influenced by species differences in testicular size; however, it is influenced by species differences in the numerical density of germ cells and in the life spans of these cells. Seminiferous tubules are composed of somatic cells (myoid cells and Sertoli cells), and germ cells (spermatogonia, spermatocytes, and spermatids). Activity of these three germ cells divide spermatogenesis into spermatocytogenesis, meiosis, and spermiogenesis, respectively. Spermatocytegenesis involves mitotic cell division to increase the yield of spermatogenesis and to produce stem cells and primary spermatocytes. Meiosis involves duplication and exchange of genetic material and two cell divisions that reduce the chromosome number and yield four spermatids. Spermiogenesis is the differentiation of spherical spermatids into mature spermatids which are released at the luminal free surface as spermatozoa. The spermatogenic cycle is superimposed on the three major divisions of spermatogenesis. Spermatogenesis and germ cell degeneration can be quantified from numbers of germ cells in various steps of development throughout spermatogenesis, and quantitative measures are related to number of spermatozoa in the ejaculate. Germ cell degeneration occurs throughout spermatogenesis; however, the greatest impact occurs during spermatocytogenesis and meiosis. Efficiency of spermatogenesis is related to the amount of germ cell degeneration, pubertal development, season of the year, and aging of humans and animals. Number of Sertoli cells and amount of smooth endoplasmic reticulum of Leydig cells (but not Leydig cell number) are related to efficiency of spermatogenesis. In humans, efficiency of spermatogenesis is reflected in number of spermatogenic stages per cross-section and number of missing generations within each stage; however, the arrangement of stages along the tubular length does not reflect differences in the efficiency of spermatogenesis. In short, spermatogenesis involves both mitotic and meiotic cell divisions and an unsurpassed example of cell differentiation in the production of the spermatozoon, and daily sperm production per g parenchyma is a measure of its efficiency.

Sertoli cells in testes containing or lacking germ cells: A comparative study of paracrine effects using the W (c‐kit) gene mutant mouse model

Paracrine effects of germ cells on Sertoli cell structure were examined in a mouse model with the W locus (dominant white spotting) mutation in which animals with the W/Wv genotype (referred to as mutants) lack virtually all germ cells. Morphometric determination of Sertoli cell parameters in mutant and control (+/+) animals showed that although the testes of mutant animals were about eight times smaller than controls, the numbers of Sertoli cells in the two groups did not differ. Sertoli cell volume, Sertoli cell cytoplasmic and nuclear volumes, and Sertoli cell surface area in mutant animals were significantly smaller than in control animals. Organelle volumes and surface areas, expressed per cell, did not differ significantly in the two groups with one exception: the volume and surface area of smooth endoplasmic reticulum was significantly reduced in mutant animals. Plasma testosterone levels and tissue testosterone levels/testis were normal, indicating that the effects observed in the mutant animal were not a consequence of androgen insufficiency. Plasma FSH was elevated, probably as a consequence of germ cell depletion, and was thought not to affect Sertoli cell parameters observed. The data suggest that paracrine interactions with germ cells do affect Sertoli cells by modifying the amount of smooth endoplasmic reticulum. These data focus attention on the function of this abundant Sertoli cell organelle in promoting spermatogenesis.

An ultrastructural study of nonfunctioning adrenocortical adenoma

Nonfunctioning adrenocortical adenomas obtained from 40 and 60-year-old males were examined by electron microscopy. Light microscopically, the tumors were shown to consist of clear cells and compact cells in both cases. However, compact cells predominated in the former case, and clear cells in the latter. Electron microscopy revealed that most of the cells in the former case had abundant organelles, including well-developed, smooth and rough endoplasmic reticulum, Golgi apparatus, and mitochondria with elaborate tubulovesicular cristae. The findings resembled those of adenomas with Cushing's syndrome. The latter case revealed a majority of cells with numerous, large lipid vacuoles, moderate amounts of smooth endoplasmic reticulum, Golgi apparatus, and mitochondria with sparse lamellar cristae resembling features of aldosteronoma. These ultrastructural findings suggest that even nonfunctioning adrenocortical adenomas, like functioning adrenocortical adenomas, have some possibility of producing adrenal hormones.

Morphology of the large granular alveoli of the parotoid glands in toad ( Bufo ictericus) before and after compression

The parotoid glands of toads are constituted by an accumulation of venom-producing granular alveoli. Parotoid glands of Bufo ictericus were manually compressed and immediately excised. Normal glands (not submitted to compression) were also excised and processed for histological and ultrastructural observations. The glandular body of large granular alveoli in parotoid glands is formed by a myoepithelial layer, internally covered by a syncytial secretory layer. In the normal parotoid gland this layer is very electron dense, thus preventing clear visualization of organelles. Large secretion granules are located in the main secretion mass, near the syncytium. In the compressed parotoid gland, the myoepithelium shows a number of alterations, including presence of myelin figures and foci of degradation in the cytoplasm. The organelles of the syncytial cytoplasm are easily observed. The mitochondria are swollen; the cristae are shortened or absent. Syncytial secretion granules and lengthened structures linked to the syncytial matrix are to be seen. A large amount of smooth endoplasmic reticulum is present, while the rough endoplasmic reticulum is reduced. This large quantity of smooth endoplasmic reticulum suggests enhanced synthesis of the cardiotoxic steroids of the venom. Alterations in the mitochondria and the presence of myelin figures and degenerative foci in the cytoplasm may probably be regarded as consequences of the cellular injury provoked by compression.

Δ5-3-β-Hydroxysteroid dehydrogenase activity in rat oviduct and implications of oviductal steroidogenesis

Tubal factor in infertility is about one third. As part of an ongoing study of the mammalian oviduct the rat oviduct was serialised into 66 zones for the characterisation of 3β-hydroxysteroid dehydrogenase activity using substrates dehydroepiandosterone (DHA), pregnenolone and testosterone. Reactivity was quantified from 1–5 and was present in some of the preampullary zones of the rat oviduct in stromal and epithelial cells and completely absent in isthmic zones. Ultrastructural analysis of oviduct ampullaryisthmic zone 33 showed a probable epithelial steroidogenic cell with considerable amounts of smooth endoplasmic reticulum and hooded and circumnuclear mitochondria. The localisation of sterol dehydrogenase activity in some zones of the preampullary-ampullary segments in the rat oviduct opens up potentialities for the study of steroidogenesis in the mammalian oviduct. If the mammalian oviduct produces considerable amounts of steroids in some zones, as the histochemical activity demonstrates, then conditions such as luteinised unruptured follicle (LUF; with diagnostic peritoneal decrease in steroid concentration), steroid presence in oviductal fluid, ovulation control by the oviduct and even oocyte maturation and local steroid-peptide interactions are easily explainable. Without the zones model, it will not be possible to characterise the activity.