Ultrastructural localization of some phosphatases in the prothoracic gland of the insect Leucophaea Maderae

Summary The cytochemical localization of acid phosphatase and thiamine pyrophosphatase activity was studied by light and electron microscopy in prothoracic gland cells of the cockroach Leucophaea moderae. Nymphal and young adult animals were used.Prominent sites of acid phosphatase activity included large membrane-bounded dense bodies or lysosomes, and certain cisternae of the Golgi apparatus. The results suggest a possible difference in the enzymatic activity toward glycerophosphate and aromatic phosphates as substrates.Thiamine pyrophosphatase activity was localized in elements of the Golgi apparatus and endoplasmic reticulum, and in lysosome-like dense bodies. This latter activity was abolished by sodium fluoride treatment, whereas the phosphatase activity in the Golgi apparatus and endoplasmic reticulum is unaffected by such inhibition.The cytochemical results confirm through direct evidence the suggestions of Scharrer (1964), that the large dense bodies present in the prothoracic gland cells are lysosomes, and that their activity may be related to stages in the life history of the glands. Furthermore, the lysosomes or their derivative structures may play an essential role in the autolysis of the prothoracic glands toward the end of their active period.The enzymatic activity of the endoplasmic reticulum may indicate the involvement of this organelle in the metabolism of steroid-like precursor materials necessary for the synthesis of ecdysone.This study was supported by U.S.P.H.S. grants 5 T1-MH-6418 and NB-05219, and grant RO 1-AM-3984 to Dr. Berta Scharrer. I would like to express my appreciation to Dr. Scharrer for her encouragement and assistance during this study. I also wish to thank Mrs. Sarah Wurzelmann for her competent technical aid.     

The fine structure of blattarian prothoracic glands

Summary The ultrastructural characterization of the prothoracic glands derives interest from the fact that they are the only known source of a steroid hormone (ecdysone) among invertebrates. The present material includes nymphal glands of two blattarian species studied at graded intervals over a period of several intermolt cycles.Among the prominent cytological features of this organ are long and intricately interwoven cellular processes that may be separated from each other by extracellular channels with an average width of 0.5 . The plasma membranes of the cells facing these spaces are coated by an external lamina (boundary membrane) representing extensions of the same extracellular material that provides the connective tissue sheath of this and other insect organs. Micropinocytotic caveolae and vesicles present along this large cellular surface area may facilitate the transport of material between glandular cells and hemolymph, or vice versa.The cytoplasm contains a fairly moderate amount of membranous structures. Golgi units are distinctive but never spectacular; ergastoplasmic elements are sparse in most cells. This sparsity as well as the absence of membrane-bounded secretory granules is in line with the known steroidal nature of the secretory product involved. Some cells show a striking array of microtubules.Certain structural attributes of nucleoli, mitochondria, and lysosome-like bodies seem to vary in conjunction with distinct phases of the intermolt cycle.Dedicated to an inspiring teacher and loyal friend, Professor F. Wassermann on the occasion of his 80th birthday, August 13, 1964. — Supported by Research Grants AM-03984 and NB-02145 from the U.S.P.H.S. — I wish to thank Mrs. Cynthia Jones and Mr. Stanley Brown for their skillful assistance.     

Particles resembling microbodies in normal and neoplastic perianal glands of dogs

Summary By electron microscopy, the parenchymal cells of the perianal glands of dogs contain granules which have the morphological features of microbodies (peroxisomes) including marginal plates and, occasionally, dense nucleoids. Like microbodies, they are occasionally attached to the endoplasmic reticulum. Histochemical evidence is presented suggesting that they contain at least one of the peroxisomal enzymes, L--hydroxy acid oxidase. The granules of a perianal gland adenoma showed abnormal morphologic variations.Mrs. Murtie Still, Mrs. Bertha McClure and Mr. Bob White gave valuable technical assistance.     

The effects of cyanide plus β-hydroxybutyrate on changes in mitochondrial absorbancy and ultrastructure induced by hypotonicity and inorganic phosphate

Summary Absorbancy measurements and electron microscopy of isolated rat liver mitochondria show that simple osmotic swelling is not prevented by cyanide plus -hydroxybutyrate. Similarly, electron microscopy shows that these two agents do not prevent the swelling induced by inorganic phosphate. However, the absorbancy decrease induced by inorganic phosphate is inhibited by cyanide plus -hydroxybutyrate.These findings cast doubt on the validity of the absorbancy method as an index of mitochondrial morphology. The evidence also indicates that both simple osmotic swelling and that induced by inorganic phosphate are independent of respiration. An osmotic mechanism is proposed as an alternative.Dedicated to Prof. Berta Scharrer on her 60^th birthday.This study was supported by Research Grants GM-08900, NB-02145, NB-05219 from the U.S.P.H.S. and a Lederle Medical Faculty Award. Fine technical assistance was provided by Mrs. Cynthia Jones, Miss Ursula Moeller and Mr. Stanley Brown.     

Ultrastructural study on the release of neurosecretory material from the sinus gland of the land crab,Gecarcinus lateralis

Summary Sites of release of neurosecretory material were examined in a neurohemal organ of decapod crustaceans, the sinus gland of the land crab, Gecarcinus lateralis. Such discharge into the circulation seems to occur primarily at interfaces between the neurosecretory axons and the acellular stromal sheath which is interposed between parenchyma and hemolymph. The evidence obtained from electron micrographs of adult specimens indicates that more or less intact secretory granules are released into the extraaxonal space primarily by the process of exocytosis. Synaptic-type vesicles are clustered in parts of neurosecretory axons facing the stromal sheath. Such vesicles are thought to result from rearrangement of membranes temporarily fused at the release site and to a minor degree from fragmentation of neurosecretory vesicles within the axon. The presence of nonmarginal vesicles and the occasional appearance of free intraaxonal dense material are interpreted as indications of a second, probably less frequent, mode of release of neurosecretory material.Supported by grants AM-3984, NB-00840, and NB-05219 from the U.S.P.H.S., administered by Dr. Berta Scharrer.I am greatly indebted to Mrs. Sarah Wurzelmann for her excellent technical assistance. I thank Dr. Dorothy E. Bliss for contributing the animals used in this study, and Mr. Murray Altmann for technical advice.     

Ring gland and prothoracic gland sensitivity to interspecific prothoracicotropic hormone extracts

Summary Using the techniques of intraspecific in vitro activation of prothoracic glands and ring glands by serial dilutions of prothoracicotropic hormone (PTTH) extracts from pupalManduca sexta (Lepidoptera) and larvalSarcophaga bullata (Diptera), a dose-response of activation was observed for both species. In both species maximum activation was at 0.5 brain equivalents while the number of brain equivalents necessary for half maximal stimulation (ED₅₀) was 0.20 forManduca and 0.15 forSarcophaga. When prothoracic glands or ring glands were challenged with interspecific PTTH extracts from a stage different from that of the gland donor, no dose-response of gland activation was observed. However, whenM. sexta larval prothoracic glands were challenged byS. bullata larval PTTH extract, activation was observed. The dose-response profile fell midway between the dose-response curves obtained for the intraspecific assays. Thus, PTTH extract from one insect has the ability to activate the prothoracic glands of an insect representing another order.     

Neurosecretion

Summary Ultrastructural changes were examined in corpora cardiaca ofPeriplaneta americana in which acute electrical stimulationin vitro had brought about hormone release.Tissue specimens from which a substantial amount of cardioaccelerator substance had been discharged into the incubation medium showed morphological indications of an increased rate of release of neurosecretory substance. These consisted in the presence, after stimulation, of a greater number of synaptoid configurations whose properties and distribution implicate them as sites of neurohormone release. This interpretation, originally arrived at by an analysis of corpora cardiaca not stimulated by experimental procedures, and fixedin situ, is now strengthened by the cytophysiological response observed as a consequence of the stimulus.According to the type of neurosecretory axon in which the formation of synaptoid structures occurs, apparently on demand, the cardioaccelerator tested for in the presentin vitro experiments, seems to be derived from large neurosecretory granules stored within the corpus cardiacum. On the basis of morphological and physiological information, their site of origin may be the perikarya of intrinsic or extrinsic neurosecretory neurons or possibly both.Supported by grants AM-3984, NB-00840, NB-04989, and NB-05219 from the U.S.P.H.S., and N.S.F. GB-4847. — We are indebted to Mrs.Sarah Wurzelmann for her excellent technical assistance.Grantee of an NDEA Title IV Predoctoral Fellowship.     

Regulation of Heliothis virescens prothoracic glands by Cardiochiles nigriceps polydnavirus

Heliothis virescens (F.) Larvae parasitized by the endophagous braconid Cardiochiles nigriceps Viereck fail to attain the pupal stage. This developmental alteration is caused by both an inactivation of prothoracic glands of last-instar larvae and an altered ecdysone metabolism. Decrease in ecdysteroidogenesis in vitro was already evident in glands explanted from larvae that have attained the early cell formation stage (day 4 of fifth instar), 6 h after parasitoid oviposition. Ecdysteroidogenesis nearly ceased by 24 h after parasitoid oviposition. The degree of this biosynthetic depression increased as the time between parasitization and gland dissection increased. A time-course study allowed us to determine if both the degree of phosphorylation of regulatory target proteins, the rate of general protein synthesis and ecdysteroidogenesis decreased in concert over time. The results provide further evidence in support of the hypothesis that these cellular activities in prothoracic gland cells are functionally correlated in steroidogenic responses. Treatment with calyx fluid and venom of C. nigriceps duplicates the parasitism-induced inactivation of host prothoracic glands. A 6-h conditioning in vitro of pupally committed host prothoracic glands with these parasitoid female reproductive secretions resulted in a significant depression of their ecdysteroid production. However, glands lost their sensitivity to calyx fluid and venom treatment when explanted from hosts that had already attained the cell formation stage. This was further supported by the fact that nearly all the host larvae parasitized on day 4 of fifth instar (cell formation stage) pupated, while parasitization on day 3 resulted in only 11% pupation. The coupled trioxsalen/UV irradiation treatment of C. nigriceps calyx fluid and venom eliminated their negative effect on biosynthetic activity in vitro by host prothoracic glands. This result indirectly demonstrates that C. nigriceps polydnavirus is the major regulating factor involved in the host prothoracic gland inactivation. Arch. Insect Biochem. Physiol. 38:1–10, 1998. © 1998 Wiley-Liss, Inc.     

Cells with microvillous borders in the cerebral ganglion of Leptodora kindtii focke (Crustacea)

Summary Groups of large cells in the cerebral ganglion of Leptodora kindtii join in intricate patterns to enclose lacunar spaces. The cell surfaces bordering on these lacunae are covered by long, densely packed microvilli that all but fill the spaces. Near their brush borders the cells are joined by adhesion plates; for the rest they are separated from each other by glial septa. The possible significance of these structures is discussed.Dedicated to an inspiring teacher and loyal friend, Prof. F. Wassermann on the occasion of his 80th birthday, August 13, 1964.Supported by Grant No. NB-02145 from the United States Public Health Service. The expert assistance of Mrs. Cynthia Jones, Mrs. Sarah Wurzelmann, and Mr. Stanley Brown is gratefully acknowledged.     

Cytologic and metabolic parameters of pineal inhibition by continuous light in the rat (Rattus norvegicus)

Summary Adult rats (Rattus norvegicus) were subjected to continuous light or control conditions (14 hours light/day) for six weeks or longer, and quantitative cytological and metabolic studies were made of the pineal organs. After 11 weeks of continuous light, the pineal parenchymal cell's largest nucleolar eosinophilic mass is significantly reduced in diameter, especially in the medulla of the organ. Evidence of metabolic inhibition includes reduction of pineal glycogen content, succinic dehydrogenase activity, and respiration in the absence of exogenous substrates. Pineal ATP content, P³²-phosphate uptake and 5-hydroxy indole acetic acid content did not appear to be affected. Pineal serotonin content and melatonin-forming activity in the continuously lighted animals were measured but could not be interpreted metabolically, due to the diurnal fluctuations of these in control animals. Results provided here and elsewhere suggest that pineal inhibition by continuous light involves primarily the citric acid cycle, the accumulation of metabolites and lipid, and the synthesis of protein.This investigation was supported by grant GM-05219 from the National Institutes of Health, U.S. Public Health Service.I am grateful to Mrs. Virginia Green Bowers, Mrs. Ann Richards, Mr. Peter Charles Baker and Mr. Jorge Antonio Alvarado for laboratory assistance, and to Dr. Richard Strohman and Mr. David Epel, for advice on the determination of ATP.     

Ultrastructure of prothoracic glands during larval-pupal development of the tobacco hornworm,Manduca sexta: A reappraisal

The structure of Manduca sexta prothoracic glands was investigated using a protocol that preserves membranes. During the last larval stadium, prothoracic gland cells increase in diameter, volume, protein content, and perhaps number, enhancing their capacity to produce ecdysteroids. The glands' strand-of-cells morphology, their in situ location, the presence of gap junctions between cells, and junctional foot-like structures within cells support previous findings that prothoracicotropic hormone stimulates ecdysteroidogenesis via Ca²⁺-induced Ca²⁺ release. A different method of tissue fixation from that previously used to investigate the ultrastructure of Manduca sexta prothoracic glands has revealed a significantly different ultrastructure. These new findings begin to define roles for endoplasmic reticulum and mitochondria in ecdysteroid synthesis and support the hypothesis that the glands secrete the steroid hormone via exocytosis. The structural dynamics of the glands are discussed in the context of the glands' function during Manduca sexta larvalpupal development. © 1993 Wiley-Liss, Inc.     

Localization of melanin synthesis within the pigment cell: Determination by a combination of electron microscopic autoradiography and topographic planimetry

Summary Localization of melanin synthesis within the pigment cells of the Cloudman S-91 mouse melanoma was determined by means of a combination of high resolution autoradiography and topographic planimetry. Initial melanin biosynthesis occurred predominantly in the endoplasmic reticulum and associated ribonucleoprotein particles of the melanocytes. By measuring a number of cell organelles and employing the index of relative specific localization it could be shown that the nucleus and mitochondria are of little or no importance in the process of melanogenesis.This investigation has been supported by the following research grants: CA 06548 CB, NIH, PHS and an Institutional Grant from the American Cancer Society (to H. M. H.); CA-05887, NIH, PHS (to A. S. Z.); M-00388 and NB-00782, NIH, PHS (to J. F. H.). One of us (H. M. H.) holds a Research Cancer Development Award (5-K 3-GM-2634) of the National Institute of General Medical Sciences, Public Health Service.We are grateful to Mr. Ronald Abler for his help with the topographic measurements; to Dr. Erhard Haus for help and advice; to Mr. J. Thornby and Mr. A. P. Basu for assistance with the statistical aspects of this study; and to Mrs. Lenore Mottaz, Miss Bernice Uittenbogaard, and Mrs. Judith Strong for careful technical assistance.     

Involvement of PI3K/Akt signaling in PTTH-stimulated ecdysteroidogenesis by prothoracic glands of the silkworm, Bombyx mori

The prothoracicotropic hormone (PTTH) stimulates ecdysteroidogenesis by prothoracic gland in larval insects. Previous studies showed that Ca²⁺, cAMP, extracellular signal-regulated kinase (ERK), and tyrosine kinase are involved in PTTH-stimulated ecdysteroidogenesis by the prothoracic glands of both Bombyx mori and Manduca sexta. In the present study, the involvement of phosphoinositide 3-kinase (PI3K)/Akt signaling in PTTH-stimulated ecdysteroidogenesis by B. mori prothoracic glands was further investigated. The results showed that PTTH-stimulated ecdysteroidogenesis was partially blocked by LY294002 and wortmannin, indicating that PI3K is involved in PTTH-stimulated ecdysteroidogenesis. Akt phosphorylation in the prothoracic glands appeared to be moderately stimulated by PTTH in vitro. PTTH-stimulated Akt phosphorylation was inhibited by LY294002. An in vivo PTTH injection into day 6 last instar larvae also increased Akt phosphorylation of the prothoracic glands. In addition, PTTH-stimulated ERK phosphorylation of the prothoracic glands was not inhibited by either LY294002 or wortmannin, indicating that PI3K is not involved in PTTH-stimulated ERK signaling. A23187 and thapsigargin, which stimulated B. mori prothoracic gland ERK phosphorylation and ecdysteroidogenesis, could not activate Akt phosphorylation. PTTH-stimulated ecdysteroidogenesis was not further activated by insulin, indicating the absence of an additive action of insulin and PTTH on the prothoracic glands. The present study, together with the previous demonstration that insulin stimulates B. mori ecdysteroidogenesis through PI3K/Akt signaling, suggests that crosstalk exists in B. mori prothoracic glands between insulin and PTTH signaling, which may play a critical role in precisely regulated ecdysteroidogenesis during development.     

An ultrastructural analysis of the ecdysoneless ((l(3)ecd 1ts) ring gland during the third larval instar of Drosophila melanogaster

Summary In the late third larval instar of Drosophila melanogaster, the prothoracic gland, an endocrine portion of the ring gland, synthesizes ecdysteroids at an accelerated rate. The resultant ecdysteroid titer peak initiates the events associated with metamorphosis. The normal prothoracic gland displays several ultrastructural features at this developmental stage that reflect increased steroidogenic activity, including extensive infoldings of the plasma membrane (membrane invaginations) and an increase in both the concentration of smooth endoplasmic reticulum (SER) (or transitional ER) and elongated mitochondria. By contrast, the prothoracic glands of larvae homozygous for a conditional larval lethal mutation, l(3)ecd ^1ts, not only fail to produce ecdysteroids at normal levels at the restrictive temperature (29° C), but also acquire abnormal morphological features that reflect the disruptive effects of the mutation. These abnormalities include an accumulation of lipid droplets presumed to contain sterol precursors of ecdysteroids, a disappearance of SER and a drastic reduction of membrane invaginations in the peripheral area of the cell. These morphological defects are observed in prothoracic glands dissected from larvae transferred from 18° C to 29° C approximately 24 h before observation and also within 4 h of an in vitro transfer to 29° C following dissection from wandering third instar larvae reared at 18° C. No ultrastructural abnormalities were noted in the corpus allatum portion of mutant ring glands. These observations further indicate the direct involvement of the ecd gene product in ecdysteroid synthesis and suggest a role for the gene in the proper transport of precursors to the site where they can be utilized in ecdysteroid biosynthesis.     

Photoperiodic and osmotic influences on the ultrastructure of the hypothalamic neurosecretory system of the White-crowned sparrow,Zonotrichia leucophrys gambelii

Summary An attempt was made to correlate functional changes in the neurohypophysis of the White-crowned Sparrow, Zonotrichia leucophrys gambelii, with morphologic features on the light- and electron-microscope levels. The aldehyde-fuchsin-staining anterior median eminence possesses essentially the same ultrastructural features as the non-staining posterior median eminence. The axon terminals are characterized by the presence of a large number of small vesicles (approximately 400 Å in diameter) and occasional electron-dense granules. The more-or-less depleted anterior median eminence occasionally evident in the photosensitive bird showing testicular development is indistinguishable ultrastructurally from the more intensely staining median eminence generally characteristic of the photorefractory bird. In the median eminence, stainability and functional state do not seem to be correlated with changes in the type, size or number of vesicles. A slight increase in the number of granules was noted in the photorefractory bird but this was considered insufficient basis to account for differences in stainability.The pars nervosa, on the other hand, responded to osmotic stimuli (saline drinking water) by loss of stainability and decrease in numbers of elementary neurosecretory granules. Small vesicles are also present in the pars nervosa axon terminals, but are intermingled with neurosecretory granules in normal birds. Acute-osmotic birds, however, had axon terminals almost entirely occupied by small vesicles.It is to be emphasized that the pars nervosa and the median eminence are two structurally very different regions of the neurohypophysis. The basis for aldehyde-fuchsin staining in the median eminence appears to differ from that in the pars nervosa. The implications of these findings are considered in regard to hypothalamic control over gonadotropic activity in the White-crowned Sparrow.Dedicated to Professor Dr. W. Bargmann in honor of his 60th birthday.This investigation was supported by grant GB-2484 from the National Science Foundation to Professor Bern, grant GB-2819 from the National Science Foundation to Professor Mewaldt, and grant NB-01353 from the National Institutes of Health to Professor Farner. The authors wish to express their appreciation of the technical assistance of Mrs. Irene Brown, Mr. John Butchart, Sally S. Kibby, Mrs. Carol Nicoll, and Mr. John Striffler. Mrs. Emily Reid kindly prepared the histograms.     

Development of an in vitro assay for prothoracicotropic hormone of the gypsy moth,Lymantria dispar (L.) following studies on identification,titers and synthesis of ecdysteroids in last-instar females

Summary Hemolymph ecdysteroid titers and in vitro prothoracic gland ecdysteroid synthesis have been examined in last-instar larval (5th instar) females of Lymantria dispar. Ecdysteroids were quantified by radioimmunoassay and characterized by co-elution with known standards of ecdysteroids on reverse-phase high-performance liquid chromatography. Analysis of hemolymph yielded ecdysone and 20-OH-ecdysone in ratios of 1:1 (day 6, shortly after attainment of maximum weight) and 1:28 (day 10, molting peak). Analysis of in vitro culture media from glands challenged with extracts of brains or retrocerebral complexes, or left unchallenged, revealed only immunoreactive material co-eluting with a known standard of ecdysone. Time-course studies of in vitro prothoracic gland ecdysone secretion demonstrated a major peak on day 10, 1–2 days prior to pupal ecdysis, and a small elevation on days 5–6. On days 5 and 6, 2.29±0.41 and 2.65±0.72 ng ecdysone per gland, respectively, were secreted in 6-h cultures. On day 10, 25.69±4.36 ng was secreted in 6-h culture. The ability of prothoracic glands of various ages to respond to brain extracts containing prothoracicotropic hormone activity was tested by determining an activation ratio for each day of the instar. The activation ratio was determined over a 90-min period by dividing the amount of ecdysone secreted by one member of a pair of prothoracic glands in the presence of brain extract by that of its contralateral control gland in Grace's medium. Prior to the addition of brain extract, the activity of the glands was allowed to subside to basal level for 180 min in Grace's medium. The activition ratio was highest on days 3–7 and fell throughout the remainder of the instar as the inherent ability of the prothoracic gland to maintain high levels of ecdysteroid synthesis in vitro in the absence of prothoracicotropic hormone increased. A two-phase in vitro assay for prothoracicotropic hormone was established using activition ratios. This assay showed saturable doseresponse kinetics for prothoracic gland ecdysone secretion and specificity to extracts prepared from brain or retrocerebral complexes. A comparable assay for prothoracicotropic hormone purification, based on net synthesis and requiring half the number of prothoracic glands was also established.Abbreviations A _r activation ratio - HPLC high performance liquid chromatography - HPSEC high performance size-exclusion chromatography - PG prothoracic gland - PTTH prothoracicotropic hormone - RIA radioimmunoassay     

The ultrastructure of monkey eccrine sweat glands

Summary The ultrastructure of monkey eccrine sweat glands is described. The secretory portion of the sweat gland is discussed in detail. The morphological differences in the secretory coil using three different fixatives and fixative combinations are emphasized. The secretory product of dark cells is seen to have three distinct appearances depending upon the fixative used. The biochemical significance of the latter finding is discussed. The appearance of clear cell cytoplasmic processes is described using the different fixatives. The similarity of adjacent clear cell processes to those of avian salt glands is pointed out and discussed. Evidence is presented to indicate that dark cells arise from clear cells via an intermediate cell type. The appearance of the clear cell plasma membrane is described and the necessity for the use of the general term multilaminar plasma membrane is discussed.Supported by U.S.P.H.S. grant 5 T 1-GM-29 F-04 AS. The author would like to express his gratitude to the Lederle Laboratories and in particular to Dr.James Vickers for providing the tissue. Sincere thanks is given to Mrs.Dagmar Graham and Mrs.Ditza Springer for technical assistance and also to MissMary Lorenc for preparation of the diagram. In addition, I would like to thank Dr.J. A. G. Rhodin for his criticism and advice.     

Histochemistry of the glands associated with the reproductive tract ofLymnaea stagnalis

Summary The albumen gland, the muciparous gland and the oöthecal gland of female genital tract of Lymnaea stagnalis, collected in spring, autumn and winter have been studied.The reactions for polysaccharides, proteins and RNA have been performed in order to characterise the secretion of the glands.The albumen gland secretion consists almost exclusively of slightly acid polysaccharides whose histochemical reactions, according to Lison and Grainger and Shillitoe confirm the presence of galactogen. Proteins are also present in the secretion. The muciparous gland secretion consists of strongly acid mucopolysaccharides (non sulphated) produced by large cells among which small cells containing sulphated mucopolysaccharides are present.In the oöthecal gland two zones are present, one with a single type of cells containing acid mucopolysaccharides, and the other with two different types of cells: the first with mucopolysaccharides and the second with sulphated mucopolysaccharides, proteins and glycogen at the basis of the cell. Sialic acids are not present in the secretion of the glands studied.The polysaccharidic composition of the secretion of the glands is different from gland to gland. The secretion of the glands gradually changes and gets acid according to the composition of the various membranes and envelopes wrapping up the eggs.     

A photosensitive circadian oscillator in an insect endocrine gland: photic induction of rhythmic steroidogenesis in vitro

The paired prothoracic glands of the insect Rhodnius prolixus each comprise a group of about 200 structurally identical cells. The synthesis (and release) of steroid moulting hormones (ecdysteroids) by these glands is under circadian control in vivo. We monitored ecdysteroid synthesis by single glands during long-term incubations in vitro. Synthesis is rhythmic in vitro and persists in continuous darkness. Glands which are arrhythmic (from prolonged continuous light) respond to transfer to darkness in vitro with the initiation of a free-running circadian rhythm of ecdysteroid synthesis. Therefore, the glands possess a light-sensitive circadian oscillator. These properties are conventionally associated with nervous tissue of animals. It is suggested that rhythmicity is synchronized within the gland by the known structural and electrical coupling between its component cells. The glands share properties with known pacemakers such as the avian pineal. However, the glands in vivo receive input from both light cues and the cerebral neuropeptide, prothoracicotropic hormone. Rhythmic release of this neuropeptide is controlled by a second oscillator located in the brain. We conclude that the pacemaker in the endocrine system of R. prolixus comprises at least three oscillators, one in each prothoracic gland and one in the brain, which are coupled hormonally. We conclude that the prothoracic gland is an important component of the circadian system controlling development in R. prolixus and that peripheral endocrine glands may play a more active role in the generation of animal circadian organization than has been thought. Accepted: 30 August 1997