Triacylglycerols characteristic of porpoise acoustic tissues: molecular structures of diisovaleroylglycerides.

More than two-thirds of the triacylglycerols from the acoustic tissues of the porpoise (Tursiops gilli) consist of 2 moles of isovaleric acid for every 1 mole of long-chain acids. Cranial blubber, which has no distinct acoustic function, does not contain these unusual glycerides. The presence of large amounts of diisovaleroylisopentadecanoylglycerol suggests that this structure may be particularly important in sound transmission through lipid-protein matrices.

Distribution of GABA-like immunoreactivity in the brain of the honeybee.

The distribution of GABA-like immunoreactivity in the brain of the honeybee was investigated with antisera generated against GABA protein conjugates. The binding of the antisera in paraffin serial sections was studied with the peroxidase-antiperoxidase method. GABA-like immunoreactive fibers appeared in all main neuropile areas. The staining of the optic lobes showed pronounced stratification. The receptor cells of compound eyes, ocelli, and antennae were not labelled. Several prominent fiber tracts showed GABA-like immunoreactivity, whereas other tracts were devoid of staining. There are no major immunoreactive commissures linking the two brain hemispheres with the exception of small commissures that bridge short distances between the beta-lobes and the antennal lobes. Several fibers in the cervical connective were also labelled; some of those may descend from the suboesophageal ganglion to the thoracic ganglia. The dense reactivity seen in the optic and antennal neuropiles implies that GABA is more important in mediating local rather than more distant neural interactions.

High substance P-like immunoreactivity (SPLI) in the olfactory and electrosensory cells of gymnotid fish.

Substance P has been proposed as a candidate neurotransmitter or neuromodulator in the nociceptive system. Using a light microscopial immunohistochemical peroxidase-anti-peroxidase technique we have detected high substance P-like immunoreactivity (SPLI) in several types of sensory organs of 4 species of gymnotiform teleost fish: olfactory epithelium, vestibular, lateral line and electrosensory organs. The olfactory nerve and its endings within the olfactory bulb and the telencephalon were also strongly labelled. At these sites no SPLI was revealed in other teleosts (Carassius auratus, Gnathonemus petersii). The findings suggest that substance P may be involved in neurotransmission or neuromodulation in these specific sensory systems of these species.

Pheromone receptors in Bombyx mori and Antheraea pernyi. II. Morphometric analysis.

Sensilla trichodea of the silk moths, Antheraea pernyi and Bombyx mori, were reconstructed from serial sections after freeze substitution. The volume and surface area of the different sensillar cells were calculated from the area and circumference of consecutive section profiles. A. pernyi and B. mori differ largely in the size of the sensory hair and the larger outer dendritic segments as well as in the volume of the receptor lymph within the hair, while there are only small differences regarding inner dendritic segments, receptor-cell somata, trichogen and tormogen cells and the volume of the receptor lymph below the hair base. In each sensillum the two (or three) receptor-cell somata, dendrites, and initial axonal segments differ significantly in volume and surface. The apical cell membranes of the trichogen and tormogen cells, which border the receptor-lymph cavity and which are the presumed site of electrogenic cation pumps, are deeply invaginated and enlarged by microlamellae and microvilli, so that their area is twice that of the remaining basolateral cell membrane. In contrast to mechanoreceptors, the trichogen cell is the largest auxiliary cell and has the largest apical membrane surface. The morphometric data are discussed with regard to recent electrophysiological observations.

Pheromone receptors in Bombyx mori and Antheraea pernyi. I. Reconstruction of the cellular organization of the sensilla trichodea.

The cellular organization of freeze-substituted antennal sensilla trichodea, which contain the sex pheromone receptors, was studied in male silkmoths of two species (Bombyx mori, Bombycidae; Antheraea pernyi, Saturniidae). The cellular architecture of these sensilla is complex, but very similar in both species. A three-dimensional reconstruction of a sensillum trichodeum of B. mori is presented. Two receptor cells (in A. pernyi 1-3) and three auxiliary cells are present. Of the latter, only the thecogen cell forms a true sheath around the receptor cells. A unique thecogen-receptor cell junction extends over the entire area of contact. Septate junctions occur between all sensillar cells apically, and in the region of the axonal origin basally. Gap junctions are also found between all cells except the receptor cells. The trichogen and tormogen cells show many structural indications of secretory activity and are thought to secrete the receptor lymph. Their apical membrane bordering the receptor-lymph space is enlarged by microvilli and microlamellae, but only those of the trichogen cell show regularly arranged membrane particles (portasomes), indicating secretory specialization among the auxiliary cells. Epidermal cells are found as slender pillars between sensilla, but extend apically along the non-sensillar cuticle and basally along the basal lamina.

Expression of achaete and scute genes in Drosophila imaginal discs and their function in sensory organ development.

Several kinds of sensory organs (SOs) appear in stereotyped positions on the adult Drosophila cuticle. The generation of these SOs requires the activity of the achaete (ac) and scute (sc) genes. To investigate whether ac and sc also provide spatial information for the positioning of SOs, we have analyzed the patterns of expression of these genes in the wing imaginal disc around the time that SO precursors are being specified. We find that expression coincides with and is restricted to areas of the disc where these precursors are known to be located. In the loss-of-function sc mutant, sc RNA is depleted in a single area located in the region where the precursor for the suppressed macrochaeta should be found. Moreover, some, and probably all, SOs require expression of these genes to reach the earliest detectable differentiated state. These and other results presented here, together with the finding that expansion of the areas of ac and/or sc expression causes the development of ectopic SOs, indicate that ac and sc promote the determination of SO precursors and delimit the regions of the imaginal discs where they can develop.

Adenosine triphosphatases in electroreceptor organs (ampullary organs and mormyromasts) of Gnathonemus petersii Mormyridae.

Cytochemical techniques were used for the light and electron microscopical localization of ATPase in the ampullary organ and the mormyromast, both cutaneous electroreceptors in Gnathonemus petersii (Mormyridae). At the right microscope level, two different techniques gave the same results, namely that high concentrations of the enzyme are present in the mormyromast and certain epidermal cells and weak concentrations in the ampullary organ. The enzyme was localized at the ultrastructural level using the lead capture method. It was found in the cytoplasm of type III accessory cells of the ampullary organ, in the apical cytoplasm of SC1 sensory cells and the accessory cells surrounding them and on the membrane of the SC2 sensory cells of the mormyromast. The ATPase of these various cells was inhibited by p-chloromercuribenzoate. The enzyme in the mormyromast SC1 and their accessory cells was not dependent on Mg2+ ions. However, that in the type III accessory cells of the ampullary organ and in the SC2 of the mormyromast was strictly dependent on Mg2+. In addition, there was a Ca2+-dependent ATPase in the microvilli of the SC2 of certain mormyromasts.

Immunocytochemistry of GABA in the antennal lobes of the sphinx moth Manduca sexta.

We have prepared and characterized specific rabbit antisera against gamma-aminobutyric acid (GABA) coupled covalently to bovine serum albumin and keyhole-limpet hemocyanin. Using these antisera in immunocytochemical staining procedures, we have probed the antennal lobes and their afferent and efferent fiber tracts in the sphinx moth Manduca sexta for GABA-like immunoreactivity in order to map putatively GABAergic central neurons in the central antennal-sensory pathway. About 30% of the neuronal somata in the large lateral group of cell bodies in the antennal lobe are GABA-immunoreactive; cells in the medial and anterior groups of antennal-lobe cells did not exhibit GABA-like immunoreactivity. GABA-immunoreactive neurites had arborizations in all of the glomeruli in the antennal lobe. Double-labeling experiments involving tandem intracellular staining with Lucifer Yellow and immunocytochemical staining for GABA-like immunoreactivity demonstrated that at least some of the GABA-immunoreactive cells in the antennal lobe are amacrine local interneurons. Several fiber tracts that carry axons of antennal-lobe projection neurons exhibited GABA-immunoreactive fibers. Among the possibly GABA-containing projection neurons are several cells, with somata in the lateral group of the antennal lobe, that send their axons directly to the lateral protocerebrum.

Immunocytochemical demonstration of the neurosecretory X-organ complex in the eyestalk of the crab Carcinus maenas.

An antiserum was obtained by immunizing rabbits with sinus gland extracts from Carcinus maenas. The antiserum is almost exclusively directed against neurosecretory material in the medulla terminalis X-organ (MTGXO), as demonstrated by the peroxidase--antiperoxidase (PAP) staining method in light and electron microscopic studies. Radioimmunological binding studies indicate the presence of antibodies against the crustacean hyperglycemic hormone (CHH) or the black pigment dispersing hormone (BPDH) in the antiserum. The results suggest that the neurosecretory perikarya of the MTGXO are the sites of production of CHH and/or BPDH.