The role of the accessory reproductive glands and genital ducts in egg pod formation in female Schistocerca gregaria

Removal of the accessory reproductive glands in female Schistocerca gregaria does not prevent the formation of eggplugs as expected. The egg pods formed are incomplete, with froth in the egg plug partially lacking. The extent of collapse is dependent on the time of removal of the glands. These results suggest that the genital ducts (egg calyces and lateral oviducts) play a significant role in the production of egg pod material, and the accessory glands probably participate in the process. Ligation of the glands has the same effect on egg pod structure; secretion accumulates in the glands indicating that, although the contribution made to the egg pod by the glands is small, they are not vestigial and are not acting simply as reservoirs for secretions produced distally. Cautery of the Comstock-Kellogg glands produces no visible change in egg pod structure or in method of formation, and thus their function remains undetermined. In the absence of the ventral median pouch egg masses are laid without the plug. A thin layer of nonvacuolated material is smeared over the walls of the oviposition hole, suggesting that the secretions produced in the upper regions of the genital ducts are added to or modified by an additional secretion from this gland, before being released to the exterior.     

The ultrastructure of the accessory sex organs of the male rat

Summary A systematic, comparative study of the accessory sex organs of the adult male rat was carried out after intra-aortic perfusion of the pelvic organs with glutaraldehyde. It has been revealed that although the epithelial cells of the different lobes of the prostate have many features in common, it is also apparent that the cell type of the various lobes have specific ultrastructural characteristics of its own, which morphologically distinguish it from the cell type of the other lobes. I.e.: the different lobes may be identified by their specific ultrastructural feature. It is also striking that the lobes, two-by-two, have so many morphological features in common that they may be divided in 3 subgroups. Based on the appearance of amount and localisation of the different organelles, the cells of the lateral lobe and the seminal vesicle are so alike that they morphologically may be classified as one group. Similarly, the coagulating gland and the dorsal lobe form another group, while the ventral lobe as a single form a third group. The few biochemical data from the different lobes which are accessible, seem suggestive to support this subgrouping.Since the various prostate lobes and the seminal vesicles have their homologies in man, further investigation both morphologically and biochemically should be concentrated upon the different groups instead of the single lobe.The study, which describes the different lobes and cell types in detail also show structures which have not been demonstrated within the prostatic epithelium before.     

Development of the accessory reproductive glands and genital ducts in female Schistocerca gregaria

The accessory reproductive glands of female S. gregaria are tubular extensions of the paired genital ducts, which in the mature female contain large amounts of a proteinaceous secretion used in the formation of the egg pod. In the 4th and 5th-instar female the glands are indistinguishable from the remainder of the mesodermally derived genital ducts. Towards the end of the 5th stadium, however, the accessory gland region only acquires characteristic convolutions which persist throughout the adult stages. At this time the epithelium of the entire ducts becomes reorganized into a unicellular epithelium. Only one cell type occurs throughout the length of the glands, and also in the egg calyces and lateral oviducts. The cells are inactive immediately after final ecdysis and remain in this state until the level of juvenile hormone in the haemolymph rises. The hormone acts directly on the cells triggering a rapid proliferation of organelles associated with protein secretion, and thereby increasing the volume of apical cytoplasm. Microvilli develop at the luminar plasma membrane, while irregular infoldings form at the base of the cells. As the gland matures the major organelle, the rough endoplasmic reticulum, changes from the lamellar to the vesicular form. Secretion is released into the lumen by the ‘microapocrine’ method.     

Accumulation of secretory proteins in the accessory reproductive glands of the male migratory grasshopper, Melanoplus sanguinipes: A developmental study

Production of secretion in the accessory reproductive glands of male Melanoplus sanguinipes has been examined by electrophoresis and radiolabelling. The secretion of each group of tubules (long hyaline glands, white glands, short hyaline glands, and seminal vesicles) can be resolved into more than 20 protein bands and includes several glycoproteins and, in the long hyaline and white glands only, lipoproteins. Each group of tubules has a characteristic pattern of synthesis and accumulation of proteins; that is, specific proteins appear in the secretion at particular times during sexual maturation. In allatectomized insects, the long hyaline glands accumulate very little secretion; the white glands and short hyaline glands accumulate about one-third the normal amount; and accumulation in the seminal vesicles is not affected by the operation. Allatectomy exerts its effect by inhibiting the synthesis of particular proteins. The observations are discussed in terms of juvenile hormone-specific protein synthesis in the accessory reproductive glands.     

Ultrastructure of the male reproductive accessory glands in the medfly Ceratitis capitata (Diptera: Tephritidae) and preliminary characterization of their secretions

The morphology and the ultrastructure of the male accessory glands and ejaculatory duct of Ceratitis capitata were investigated. There are two types of glands in the reproductive apparatus. The first is a pair of long, mesoderm-derived tubules with binucleate, microvillate secretory cells, which contain smooth endoplasmic reticulum and, in the sexually mature males, enlarged polymorphic mitochondria. The narrow lumen of the gland is filled with dense or sometimes granulated secretion, containing lipids. The second type consists of short ectoderm-derived glands, finger-like or claviform shaped. Despite the different shape of these glands, after a cycle of maturation, their epithelial cells share a large subcuticular cavity filled with electron-transparent secretion. The ejaculatory duct, lined by cuticle, has epithelial cells with a limited involvement in secretory activity. Electrophoretic analysis of accessory gland secretion reveals different protein profiles for long tubular and short glands with bands of 16 and 10 kDa in both types of glands. We demonstrate that a large amount of accessory gland secretion is depleted from the glands after 30 min of copulation.     

The hormonal control of accessory reproductive gland development in female Schistocerca gregaria

Allatectomy of adult female Schistocerca gregaria prevents the normal development of the accessory reproductive glands and no secretion is produced. Development of the glands can be restored by the administration of synthetic juvenile hormone and the response is dose-dependent. A continuous supply of hormone is required for maintenance of secretory activity. In the normal developmental sequence the total protein content of the glands remains constant until the time at which vitellogenesis occurs in the terminal oöcytes. As maturation proceeds there is a linear increase in protein content of the glands. The initial increase occurs as a result of cellular changes in the glands and is then followed by an increase due to an accumulation of secretion in the lumina.     

桑天牛雄性附腺内容物组分分析

测定桑天牛Apriona germaric(Hope)雄性附腺内容物中各组分含量及变化情况。结果表明,内容物中可溶性蛋白占总腺管鲜重的8.39%;总糖占总鲜重的4.21%;海藻糖和游离氨基酸分别占总鲜重的0.50%、0.25%。随虫龄的增大,内容物中各组分含量不断降低。交配过程中,雄性附腺内容物部分转移到雌虫,交配后附腺内容物中总糖、海藻糖、游离氨基酸等组分含量均降低,蛋白质组分含量先升高再降低,48h即恢复可到交配前水平。大、小附腺内各组分含量变化有差异。     

Wing morph-related differences in developmental pattern of accessory gland proteins in adult males of Pyrrhocoris apterus (L.) and their endocrine control

The study showed that the amounts of the total proteins and 53 kDa protein in male accessory glands (AGs) of the firebug Pyrrhocoris apterus (L.) increased with age of the adult life. The 53 kDa protein, the most abundant polypeptide detected in the secretion of the AGs, and some other smaller peptides were identified as glycoproteins. Changes in the amounts of the total proteins and 53 kDa protein in AGs were found to be wing morph-dependent and their levels were significantly higher in 1-10 days old brachypterous males than in macropterous males of the same age. Macropterous males were characterized by delayed growth of the AGs. Treatment of adult macropterous males with methoprene significantly increased the amounts of total proteins and 53 kDa protein in their AGs when compared to acetone-treated macropterous controls of the same age. Allatectomy of brachypterous males decreased the levels of the total proteins and 53 kDa protein in their AGs, while application of methoprene enhanced the quantity of allatectomy-suppressed proteins in these tissues. This is the first report of juvenile hormone-dependent wing morph-related differences in the synthesis of AG proteins and their endocrine control in wing-polymorphic insects.     

Evidences of the extraglandular origin of two secretory proteins in the male accessory reproductive glands of Chilo partellus (Pyralidae,Lepidoptera, Insecta)

Summary

The male accessory reproductive glands (MARG) play an important role in contributing proteins for the formation of the spermatophore, a structure that transports sperm from the male to the female. Several studies have shown that these proteins could be either of intraglandular or extraglandular origin. SDS-PAGE analysis revealed proteins in the adult MARG of Chilo partellus, which comigrate with the larval hemolymph proteins (LHP). Ouchterlony's immunodiffusion showed that the antiserum raised against MARG extract cross-reacts with the proteins present in the adult hemolymph and fat body. Immunoprecipitates of labelled hemolymph proteins with anti-LHP or anti-MARG proteins reveal two polypeptides that comigrate with LHPs. Thus, there appear to be some proteins of extraglandular origin in the MARG of C. partellus, and the LHP could belong to this category.     

Intraglandular and extraglandular synthesis of proteins secreted by the accessory reproductive glands of the colorado potato beetle,Leptinotarsa decemlineata

The accessory reproductive glands (ARGs) of the male Colorado beetle secrete about 50 polypeptides with molecular weights varying between 15,000 and 650,000. Most of these polypeptides are synthesized by the gland itself. However, some secretory polypeptides originate from the fat body and are transported to the ARGs by the haemolymph. One of these extraglandular secretory polypeptides corresponds with one of the two subunits of the major haemolymph lipoprotein. The second subunit of this lipoprotein is not secreted, but is accumulated at the microvillar zone of the secretory cells.     

Morphological analysis of the male reproductive accessory glands of the bat Artibeus lituratus (Phyllostomidae: Chiroptera)

Bats are distributed worldwide from tropical to temperate regions. Despite their wide geographical radiation and advances in studies using evolutionary approaches, aspects related to the reproduction of these animals remain poorly explored, especially those related to the male reproductive accessory glands (RAGs). Thus, the aim of this study was to analyze the morphophysiology of the male RAGs in the bat Artibeus lituratus. The RAGs in A. lituratus are composed of a compact intra‐abdominal glandular complex, consisting of the prostate with two prostatic regions (ventral and dorsal), plus Littre glands and a pair of extra‐abdominal bulbourethral glands. The ventral region of the prostate has an epithelium with variable morphology, due to its holocrine type of secretion. In contrast, the dorsal region has a typical cubic‐to‐columnar pseudostratified epithelium. Both regions contain two cell types, basal and secretory cells. Similar to the epithelial morphology, the secretion also varies, with the ventral region containing numerous PAS‐positive globular vesicles, whereas the dorsal region has a more fluid, hyaline and PAS‐negative secretion. Littre glands are dispersed in the connective tissue of the urethra, while the bulbourethral glands are located in the penile root, both glands with cubic‐to‐columnar pseudostratified epithelium and globular PAS‐positive secretion. The results demonstrate that the RAGs of A. lituratus are composed of two prostatic regions, ventral and dorsal, and urethral and bulbourethral glands, with no seminal vesicles. Each prostatic region has unique and distinctive characteristics, with the ventral region presenting an exclusive holocrine nature and the dorsal region having similarities to the ventral prostate of rodents.     

Juvenile hormone regulation of male accessory gland activity in the red flour beetle, Tribolium castaneum

Male accessory gland proteins (Acps) act as key modulators of reproductive success in insects by influencing the female reproductive physiology and behavior. We used custom microarrays and identified 112 genes that were highly expressed in male accessory glands (MAG) in the red flour beetle, Tribolium castaneum. Out of these 112 identified genes, 59 of them contained sequences coding for signal peptide and cleavage site and the remaining 53 contained transmembrane domains. The expression of 14 of these genes in the MAG but not in other tissues of male or female was confirmed by quantitative real-time PCR. In virgin males, juvenile hormone (JH) levels increased from second day post adult emergence (PAE), remained high on third day PAE and declined on fourth day PAE. The ecdysteroid titers were high soon after adult emergence but declined to minimal levels from 1 to 5 days PAE. Feeding of juvenile hormone analog, hydroprene, but not the ecdysteroid analog, RH-2485, showed an increase in size of MAGs, as well as an increase in total RNA and protein content of MAG. Hydroprene treatment also increased the expression of Acp genes in the MAG. RNAi-mediated knock-down in the expression of JHAMT gene decreased the size of MAGs and expression of Acps. JH deficiency influenced male reproductive fitness as evidenced by a less vigor in mating behavior, poor sperm transfer, low egg and the progeny production by females mated with the JH deficient males. These data suggest a critical role for JH in the regulation of male reproduction especially through MAG secretions.     

Ultrastructure of the accessory glands of gene's organ in the cattle tick, Boophilus

The organization and ultrastructure of the accessory glands of the cattle tick, Boophilus microplus, are described. The glands consist of two groups of acinar cells situated on either side of Gene's organ. A single acinus consists of from eight to 12 cells and each cell is connected via an individual duct to pores on the dorsal surface of the mouthparts. The position of these pores is such that the secretion of the accessory glands is incorporated into the egg wax during oviposition. Each gland cell has striking quantities of smooth endoplasmic reticulum and numerous Golgi dictyosomes and appears to produce a secretion that is lipoidal in nature. Each cell secretes into its own individual lumen and is connected to a cuticular pore by a duct cell.     

The architecture of the accessory reproductive glands of the male desert locust. 5: ultrastructure during maturation

The accessory reproductive glands of the male desert locust were studied with the electron microscope from the time of adult emergence until full sexual maturity was attained (10 days). Observations on the changes in the nucleus and the cytoplasm of the glandular epithelium, particularly those organelles involved in the elaboration of cell secretions, were made during the maturation of the accessory glands. Cells of gland 16 (the functional seminal vesicle) exhibit numerous ribosomal aggregates, have a concentration of mitochondria along their luminal surface, and show some secretory activity, even at the time of adult emergence. On the other hand, all other accessory glands show very little development of the secretory apparatus (rough-surfaced endoplasmic reticulum, polyribosomes, Golgi elements, elaborate mitochondria, etc.) until after the fifth adult day. These changes parallel changes in the secretory activity of the adult corpus allatum; and it is suggested that the corpus allatum hormone regulates the maturation of the truly glandular accessory glands of the locust, but not that of the functional vesicle.     

Male insect accessory glands: Functions and control of secretory activity

Summary

Paralleling the diversity of the class Insecta, the male accessory glands (MAG) exhibit a wide range of form, and their secretion serves a variety of functions, including spermatophore and mating plug formation, sperm activation, provision of nutrients to females, and, through production of fecundity-enhancing and/or receptivity-inhibiting substances, modification of female reproductive behavior. In most insects, juvenile hormone (JH) is important in the regulation of MAG secretory activity; specifically, JH controls the production of particular proteins in the secretion. However, the production of some proteins appears not to be influenced by JH; rather, their synthesis is regulated by ecdysteroids. During sexual maturation, JH and ecdysteroids seem to interact to bring about a specified temporal sequence of protein synthesis in the MAG.     

Nuclear binding sites for juvenile hormone III in the male accessory reproductive glands of Melanoplus sanguinipes

Summary

We have identified a potential nuclear juvenile hormone (JH) receptor in the long hyaline tubules (LHT), part of the male accessory reproductive gland (MARG) of M. sanguinipes. The MARG was incubated in vitro with [³H]JH III, and the distribution of the [³H]JH III among the cellular fractions of the LHT was determined. Some 37±4% of the radioactivity was associated with the crude nuclear pellet, while the cytosolic, microsomal and mitochondrial fractions contained 30±3%, 23±2% and 10±1%, respectively. The bound JH III was measured in nuclear extracts of LHT from males up to 15 days post-eclosion. These results revealed that JH binding increased in an age-dependent manner up to day 7, then levelled off to day 12, to increase again on day 14. The nuclear-binding component in the LHT had a very strong affinity for JH III, with a K_D value of 0.8 nM. Our observations are considered in relation to the potential site and mode of action of JH.     

Effects of the expression of bovine growth hormone on the testes and male accessory reproductive glands in transgenic mice

The effects of physiological and excessive levels of growth hormone (GH) on reproductive functions are poorly understood, and impairment of fertility is frequently observed in transgenic animals overexpressing GH genes. The present study was undertaken to determine the effects of chronic exposure to heterologous bovine GH (bGH) on the testes and accessory reproductive glands in transgenic mice. Endocrine function of the testes was evaluated by measuring the activities of two steroidogenic enzymes, 5-3-hydroxysteroid dehydrogenase (5-3-HSD) and 17-hydroxysteroid dehydrogenase (17-HSD). The activities of acid phosphatase, alkaline phosphatase and -glucuronidase, important hydrolytic enzymes of lysosomal origin, were measured in testes, seminal vesicles and ventral prostates in normal and transgenic mice. Testicular 5-3-HSD activity was higher in transgenic than in normal mice, while testicular 17-HSD activity in transgenic mice was not altered. Acid phosphatase activity was elevated in both seminal vesicles and ventral prostates of transgenic mice, while alkaline phosphatase activity was increased only in the prostate. The activity of -glucuronidase was elevated in the testes, seminal vesicles and ventral prostate gland of transgenic mice. These results suggest that chronic exposure to bGH is associated with significant stimulation of some hydrolytic enzymes in the testes and in the accessory reproductive glands of transgenic mice.     

Characteristics of aminopeptidase activity of female housefly reproductive accessory glands

Proteolytic activity was detected in crude extracts of female reproductive accessory glands and the following characteristics of the principal aminopeptidase activities were determined: substrate specificity, pH optima, molecular weights, and effects of inorganic salts. The greatest aminopeptidase activities were found with the β-naphthylamides of: alanine at pH 7.5 and 9.5, leucine at pH 8.0, and methionine at pH 6.5. The methionine-specific activity in the crude extract was stimulated 3 times by 100 mM MgCl₂, CaCl₂, NaCl, or KCl. Inhibition was noted, and ID₅₀ was determined for each of the other principal substrates with the following salts: CdCl₂, CaCl₂, ZnCl₂, HgCl₂, MgCl₂, and MnCl₂. Molecular weights, estimated on Sephadex G-200 and on Sepharose-6B, were found to be around 210 000 for each of these principal aminopeptidase activities in the crude extract.     

A polypeptide from male accessory glands which triggers maturation of tick spermatozoa

The maturation of tick (Acari: Ixodoidea) spermatozoa, after their transfer to the female, is induced by secretions of the male accessory gland which are added to the prospermia during ejaculation. Analysis of the secretions from male Ornithodoros moubata (Argasidae) and Dermacentor variabilis (Ixodidae) indicates that the factor responsible for inducing maturation is a polypeptide with a molecular weight of about 12,500. Although the polypeptides from the two species are similar in most respects, each will not activate the prospermia of the other species. The mode of action of the factor is hormone-like, inasmuch as a few minutes of exposure of the sperm to the factor are sufficient to trigger the entire maturation sequence, which takes 12–24 h in vitro.