Analysis of milk gland structure and function in Glossina morsitans: milk protein production, symbiont populations and fecundity

A key process in the tsetse reproductive cycle is the transfer of essential nutrients and bacterial symbionts from mother to intrauterine offspring. The tissue mediating this transfer is the milk gland. This work focuses upon the localization and function of two milk proteins (milk gland protein (GmmMGP) and transferrin (GmmTsf)) and the tsetse endosymbionts (Sodalis and Wigglesworthia), in the context of milk gland physiology. Fluorescent in situ hybridization (FISH) and immunohistochemical analysis confirm that the milk gland secretory cells synthesize and secrete milk gland protein and transferrin. Knockdown of gmmmgp by double stranded RNA (dsRNA) mediated RNA interference results in reduction of tsetse fecundity, demonstrating its functional importance in larval nutrition and development. Bacterial species-specific in situ hybridizations of milk gland sections reveal large numbers of Sodalis and Wigglesworthia within the lumen of the milk gland. Sodalis is also localized within the cytoplasm of the secretory cells. Within the lumen, Wigglesworthia localize close to the channels leading to the milk storage reservoir of the milk gland secretory cells. We discuss the significance of the milk gland in larval nutrition and in transmission of symbiotic bacteria to developing offspring.     

Structural modulations in the tsetse fly milk gland during a pregnancy cycle.

Gross ultrastructural and histochemical details of the integumental milk glands of the tsetse fly Glossina morsitans have been examined during the pregnancy cycle. Structural evidence for protein secretion is found between Days 3-8 of the nine-day cycle: termination of activity is completed on the day of parturition. Onset of lactation is synchronized with the eclosion of the first instar larva. The changes in cell volume (notably in the extracellular reservoir) occurring throughout the pregnancy cycle are illustrated in electron micrographs, and a one hundred-fold volume increase in the reservoir volume between the inactive phase and the active period is illustrated and discussed in terms of membrane modulation of the limiting membrane of the reservoir. Intracellular membrane changes during the cycle, particularly the development of extensive ER arrays in the actively secreting cell, are illustrated and discussed. It is suggested that cytoplasmic microtubules play a part in maintaining the form of the distended secretory cell, at the height of secretory release and storage. Histochemical observations on the milk secretion, and the contents of the larval gut are presented.     

Storage and mobilisation of nutriment for uterine milk synthesis by Glossina morsitans

Nitrogen content of eggs and larvae of Glossina morsitans was a constant proportion of dry weight and equivalent to ca. 55% protein assuming tsetse proteins contain 16% nitrogen. The larval gut content (uterine milk) contained 40% protein. Fatty acid composition of lipids in the milk and in the larval body was similar, with Palmitic (35–38%), Palmitoleic (31–35%) and Oleic acid (23–25%) predominating. Results support the hypothesis that uterine milk contains both protein and lipid and that its composition is relatively constant throughout the period of its synthesis and secretion.Patterns of incorporation of radioactivity by fertilized adult females from injected [¹⁴C]-leucine changed throughout a pregnancy cycle. High levels of incorporation into lipid (22–30%) during early pregnancy fell to around 10% during late pregnancy. Over the same period low levels of incorporation into protein (5%) increased to 15%. Results support the hypothesis that uterine milk is synthesized from a lipid store laid down in early pregnancy coupled with protein derived largely from blood meals ingested later. Such a system would not require the insect to store proteins for larval growth and is economical in terms of energy expenditure.     

The morphogenesis of spermathecae and spermathecal glands in Drosophila melanogaster

Sperm storage in female insects is important for reproductive success and sperm competition. In Drosophila melanogaster females, sperm viability during storage is dependent upon secretions produced by spermathecae and parovaria. Class III dermal glands are present in both structures. Spermathecal glands are initially comprised of a three-cell unit that is refined to a single secretory cell in the adult. It encapsulates an end-apparatus joining to a cuticular duct passing secretions to the spermathecal lumen. We have examined spermatheca morphogenesis using DIC and fluorescence microscopy. In agreement with a recent study, cell division ceases by 36 h after puparium formation (APF). Immunostaining of the plasma membrane at this stage demonstrates that gland cells wrap around the developing end-apparatus and each other. By 48–60 h APF, the secretory cell exhibits characteristic adult morphology of an enlarged nucleus and extracellular reservoir. A novel finding is the presence of an extracellular reservoir in the basal support cell that is continuous with the secretory cell reservoir. Some indication of early spermathecal gland formation is evident in the division of enlarged cells lying adjacent to the spermathecal lumen at 18 h APF and in cellular processes that bind clusters of cells between 24 and 30 h APF.     

Development of female accessory glands of Chrysomya putoria (Wiedemann) (Diptera: Calliphoridae) during oogenesis

Females of Chrysomya putoria (Diptera: Calliphoridae) have two sexual accessory glands, which are tubular and more dilated at the distal extremity. The glands open independently into the common oviduct. Two morpho-physiological regions were distinguished in the longitudinal semi-thin sections of the glands. The secretory region is constituted by three layers: a cuticular intima, lining the lumen, followed by a layer of small cells, and then a layer of very large secretory cells. The ductal region of the gland presents only two layers: the cuticular intima and a cellular layer. In both regions a basement membrane is present. Each secretory cell has in its apical region a reservoir, which enlarges throughout oogenesis; in its basal region there is a large nucleus. The ductal cells are cylindrical and smaller than the secretory cells. The glandular secretion is synthesized in the cytoplasm of the secretory cells, stored and/or modified in the reservoir, then drained to the lumen through an end apparatus seen in the apical region of the secretory cell. Histochemical tests indicate that this secretion is a glycoprotein. Measurements of the glands from females at different physiological conditions and fed on different diets correlate with the results obtained for changes in the ovary during oogenesis. Cell number averaged 561.2 ± 77.54 per gland. There was no increase in cell number during oogenesis.     

Melophagus ovinus (Pupipara: Hippoboscidae): Confirmation of the nonpathogenicity of Trypanosoma melophagium for sheep keds

Data are presented to show that Trypanosoma melophagium is not pathogenic to the sheep ked, Melophagus ovinus. During each normal cycle of the ked population on sheep, death of variable numbers of keds occurs that cannot be attributed to host resistance. Pathological signs include abdominal swelling, reddening of the hemolymph, cessation of peristalsis, and desquamation of the epithelium of the posterior midgut. These pathological developments are attributed to hypoxia in the gut wall resulting from occlusion of abdominal spiracles with debris. They occur alike in keds infected with T. melophagium and in keds that have been made flagellate free experimentally.     

Nutrient transfer during the reproductive cycle in Glossina austeni Newst.: histology and histochemistry of the milk gland, fat body, and oenocytes

Using thick sections cut from Epon-embedded tissues fixed in Karnovsky's fixative, the cytological changes visible in the light microscope were described for milk gland, fat body and oenocytes during the pregnancy cycle of the female of Glossina austeni. Histochemical procedures on paraffin sections were used to explore changes in nucleic acids, proteins, and tyrosine-containing proteins. The milk gland undergoes a cycle of secretion correlated with the pregnancy cycle and the results are consistent with the view that the protein component of the milk is synthesized in the secretioy cells of the gland. Tyrosine is particularly abundant in the oenocytes which appear to play a crucial role in the metabolism of this amino acid.     

Expression of alpha-lactalbumin, alpha-S1-casein, and lactoferrin genes is heterogeneous in sheep and cattle mammary tissue.

We used 35S-labeled cRNA probes to localize the sites of alpha-lactalbumin, alpha-S1-casein, and lactoferrin mRNA synthesis in sheep and forcibly weaned cattle mammary tissue. Expression of alpha-lactalbumin was absent in three of four "virgin" glands studied, present in some alveoli of "pregnant" glands but not in others, despite a similar histological appearance. In the early lactating gland, expression was high in those alveoli with few fat globules in their cells and lumen and was absent in alveoli with abundant fat globules. These observations suggest either that alpha-lactalbumin gene expression is linked to the long-term secretory activity of cells and falls once cells are resting or regressing, or that there are cyclical variations in expression, or that in the lactating gland some groups of epithelial cells are synthesizing alpha-lactalbumin and some are synthesizing fat. Expression patterns of alpha-S1-casein were similar to those of alpha-lactalbumin. Lactoferrin, in contrast, was expressed almost exclusively in the "fatty alveoli" of both species. Our results show that dramatic variations in milk gene expression can occur throughout the mammary gland of sheep and cattle and that at no stage of pregnancy, lactation, or involution can the gland be considered metabolically homogeneous.     

Venom and Dufour's glands of the emerald cockroach wasp Ampulex compressa (Insecta,Hymenoptera, Sphecidae): Structural and biochemical aspects

The digger wasp species Ampulex compressa produces its venom in two branched gland tubules. They terminate in a short common duct, which is bifurcated at its proximal end. One leg is linked with the venom reservoir, the other one extends to the ductus venatus. Each venom gland tubule possesses, over its entire length, a cuticle-lined central duct. Around this duct densely packed class 3 gland units each composed of a secretory cell and a canal cell are arranged. The position of their nuclei was demonstrated by DAPI staining. The brush border of the secretory cells surrounds the coiled end-apparatus. Venom is stored in a bladder like reservoir, which is surrounded by a thin reticulated layer of muscle fibres. The reservoir as a whole is lined with class 3 gland units. The tubiform Dufour's gland has a length of about 350 μm (∅ 125 μm) only and is surrounded by a network of pronounced striated muscle fibres. The glandular epithelium is mono-layered belonging to the class 1 type of insect epidermal glands. The gland cells are characterized by conspicuous lipid vesicles. Secretion of material via the gland cuticle into the gland lumen is apparent. Analysis of the polypeptide composition demonstrated that the free gland tubules and the venom reservoir contain numerous proteins ranging from 3.4 to 200 kDa. The polypeptide composition of the Dufour's gland is completely different and contains no lectin-binding glycoproteins, whereas a dominant component of the venom droplets is a glycoprotein of about 80 kDa. Comparison of the venom reservoir contents with the polypeptide pattern of venom droplets revealed that all of the major proteinaceous constituents are secreted. The secreted venom contains exclusively proteins present in the soluble contents of the venom gland. The most abundant compound class in the Dufour's gland consisted of n-alkanes followed by monomethyl-branched alkanes and alkadienes. Heptacosane was the most abundant n-alkane. Furthermore, a single volatile compound, 2-methylpentan-3-one, was identified in various concentrations in the lipid extract of the Dufour's gland.     

Quantitative morphological changes of the uterine gland cells in relation to physiological events during a pregnancy cycle in Glossina morsitans morsitans

Secretory cells of the uterine gland were investigated morphometrically during the second pregnancy cycle in Glossina morsitans morsitans. In early pregnancy when an egg was present in the uterus, morphometric parameters of the nucleus, the cytoplasm and its organelles were markedly low coincident with low physiological activity in the gland cells. This is the period when a proportion of the assimilated amino acids from the digested blood meals are converted to triglyceride in the fat body and stored. During the second half of pregnancy, when a larva was present in the uterus, there was a striking increase of the cytoplasmic and organelle volumes as well as of the surface areas of rough and smooth endoplasmic reticulum. There was also a marked augmentation of triglyceride-like inclusions, and later of secretory vesicles which released their content into enlarging extracellular reservoirs. This indicated a markedly high activity in the gland cells concomittant with the period of rapid synthesis of large amounts of proteins and lipoproteins destined for the growing intra-uterine larva. Mitochondrial parameters also increased, probably to generate adequate energy for synthesis, transport and secretion of nutriments for the larva. After larviposition, a marked reduction of cellular parameters was measured, and the volume density of lysosome-like structures had increased, indicating that larviposition is followed by degradation of large amounts of cellular organelles involved in biosynthetic processes. Morphometrical investigation of the uterine gland cells demonstrated a temporal correlation of the cellular dynamics with physiological events involved in producing a fully developed third-instar larva at the end of a pregnancy cycle.     

Fine structure of the male accessory glands in Aedes triseriatus

The paired accessory glands of the male mosquito, Aedes triseriatus, consisted of a single layer of columnar epithelial cells enclosed by a richly-nucleated circular muscle layer. Each accessory gland is divided into an anterior gland (AG) with one type of secretory cell, and a posterior gland (PG) with two types. The cells of the AG and those of the anterior region of the PG showed macroapocrine secretion. The mucus secreting cells located at the posterior region of the PG, however, released their contents into the lumen of the gland by rupturing the apical membrane of the cell. The secretion from all cells was in the form of membrane-bound granules which had distinct electron-dense and electron-lucent areas.     

An integumentary gland secreting a territorial marking pheromone in Atta sp.: Detailed structure and histochemistry

An abdominal pheromone-producing gland in Atta sp. was examined using light and electron microscopy techniques. The gland is composed of a bunch of juxtaposed secretory units in which the secretory ductules open on to a cribellum close to the sting base.The structure and cycles of the secreting units are described. Each includes a secretory cell with an ‘end apparatus’, ductule cells and epidermal cells. The secretory cycle of glycoproteins accumulated in the ‘end apparatus’ is discussed and a functional interpretation of the morphological components of the application system is proposed.     

Dynamics of the pregnancy cycle in the tsetse Glossina morsitans

A normal pregnancy in tsetse involves the successful integration of larval development with maternal activity. At 25°C, ovulation in Glossina morsitans occurs 1 hr after the previous larviposition, the egg hatches on day 3·8 (1·57 mm length, 0·09 mg dry wt.), ecdysis to second instar occurs on day 4·9 (2·3 mm, 0·30 mg), the third instar cuticle is formed on day 6·8 (4·5 mm, 5·0 mg), and parturition occurs on day 9·0 (6·0 mm, 10·0 mg). Melanization of the in utero third instar follows a regular sequence over a 2 day period. Parturition follows a circadian pattern with a peak 9 hr after lights on (12 hr daily photophase). All instars receive nutriment from the female's milk gland. During early pregnancy the rate of milk synthesis is greater than rate of uptake by the larva, thus causing expansion of the secretory reservoirs. After day 6, the volume of the secretory reservoirs decreases, but as is indicated by nuclear volume and larval growth the rate of synthesis remains high until day 8. Feeding activity of the adult female is maximal on day 1, levels off at 60 per cent up to day 6, and then declines sharply towards the end of pregnancy. Oöcyte development proceeds in phase with larval development and thus minimizes a lag period between successive pregnancies.     

Ultrastructure and nature of secretory proteins in the male accessory gland of Drosophila funebris

The ultrastructural differentiation of the secretory cells and the nature of secretory proteins in the male accessory gland of Drosophila funebris have been studied by electron-microscopic and immunological methods. (1) In the pupae at $\text{1}\text{1}\text{2}$ days before eclosion, secretory products can be detected in the lumen, even though most glandular cells are at the initial phase of differentiation. At the time of eclosion both main and secondary cells are fully differentiated, but the whole set of five immunologically active proteins are detectable only on the second to third day of adult life. (2) The secondary cells contain giant protein granules, the so-called filamentous bodies, which become partially fused and the filaments assume a twisted form. Randomly dispersed filaments and closely packed filament bundles are also visible in the gland lumen. Antigenic labelling of ultrathin sections and immunoreplica electrophoresis yielded no evidence for the microtubular nature of these filaments. The secretion stored in the lumen contains in addition a large quantity of flocculent proteins which have their origin in the main cells. (3) During the period of high secretory activity in the 7-day-old male flies no vacuolization and disintegration of either the main or secondary cells have been observed. We conclude that both types of cells have the merocrine secretory mechanism. (4) Ultrastructural alterations in the glandular cells confirmed our previous observation that copulation stimulates RNA and protein synthesis.     

The ultrastructure and histology of the perinotal epidermis and defensive glands of two species of Onchidella (Gastropoda: Pulmonata)

Histology and electron microscopy were used to describe and compare the structure of the perinotal epidermis and defensive glands of two species of shell-less marine Systellommatophora, Onchidella capensis and Onchidella hildae (Onchidiidae). The notum of both species is composed of a layer of epithelial and goblet cells covered by a multi-layered cuticle. Large perinotal multi-cellular glands, that produce thick white sticky mucus when irritated, are located within the sub-epidermal tissue. The glands are composed of several types of large secretory cell filled with products that stain for acidic, sulphated and neutral mucins, and some irregularly shaped support cells that surround a central lumen. The products of the secretory cells are produced by organelles that are basal in position. The entire gland is surrounded by a well-developed capsule of smooth muscle and collagen, and in addition smooth muscle surrounds the cells within the glands. Based on the size of the gland cells, their staining properties, and the appearance of their stored secretions at the transmission electron microscope level, five different types of secretory cells were identified in O. capensis and four in O. hildae. The products of these cells, which are released by holocrine secretion, presumably mix in the lumen of the duct as they are forced out by contraction of the smooth muscle. The structural similarity of these glands to those of siphonariids, suggest that they have a common ancestry.