Putative neurotransmitters in the retinae of three urodele species (Triturus alpestris,Salamandra salamandra,Pleurodeles waltli)

Summary The immunocytochemical localization of several substances with putative neurotransmitter or modulator properties was investigated in the retinae of three urodele species. Gamma-aminobutyric acid-like immunoreactive labelling appeared in different types of amacrine and horizontal cells. In addition, labelled fibres in the optic nerve were detected. It was not possible to determine whether these fibres were ganglion-cell axons or part of an efferent projection. Endogenous serotonin was found in several populations of amacrine cells including stratified and diffuse types. Glucagon-like immunoreactivity appeared in one bistratified amacrine cell type, and neurotensin-like immunoreactivity was detected in a single monostratified amacrine cell type. Metenkephalin-like-immunoreactive labelling was rare but found in several sublaminae of the inner plexiform layer. Thus each peptide-like-immunoreactive cell type makes up a distinct and unique population of cells and probably has a special functional role in retinal processing. There are striking similarities in the peptide-like immunoreactive patterns of Triturus alpestris and Necturus maculosus whereas in Ambystomatidae the peptide-like-immunoreactive systems appear to be differently organized. This supports the hypothesis that Salamandridae and Proteidae are more closely related to each other than to the Ambystomatidae.Abbreviations GABA gamma-aminobutyric acid - GCL ganglion cell layer - Glu glucagon - HRP horseradish peroxidase - INL inner nuclear layer - IPL inner plexiform layer - IR immunoreactive or immunoreactivity - M-enk metenkephalin - Neu neurotensin - OFL optic fibre layer - ONL outer nuclear layer - OPL outer plexiform layer - Ser serotonin This work forms part of the doctoral thesis of Gaby Gläsener, Faculty of Biology, Technical University of Darmstadt, Federal Republic of Germany. Supported by a research grant from the Deutsche Forschungsgemeinschaft (Hi 306/1-1)     

Les tissus élaborateurs d'hormones stéroïdes chez les amphibiens urodèles

Résumé Les cellules du tissu glandulaire du testicule et de la glande interrénale de pleurodèle montrent les caractères généralement observés dans les cellules stéroïdogènes. Des différences existent entre les deux tissus. Le reticulum endoplasmique du tissu glandulaire est très développé et présent dans toutes les cellules qui sont d'aspect homogène. Au contraire, le tissu interrénal montre deux aspects cellulaires différents. Le premier se caractérise par un reticulum endoplasmique lisse relativement peu développé par rapport au tissu glandulaire, par des mitochondries petites et nombreuses, enfin par des liposomes denses et petits. Le deuxième aspect au contraire, se distingue par le petit nombre de mitochondries souvent géantes et à crêtes plus fréquemment organisées en faisceaux, par des liposomes nombreux de grandes dimensions et peu denses aux électrons.Le tissu glandulaire est très peu touché par l'hypophysectomie. Le reticulum persiste plusieurs mois comme d'ailleurs l'activité 5-3 -hydroxystéroïde deshydrogénase. Dans le tissu interrénal, la proportion des cellules d'aspects différents varie au profit des cellules à lipides abondants et à grandes mitochondries. L'activité 5-3 -hydroxystéroïde deshydrogénase est longtemps décelable.Le rôle du reticulum endoplasmique du tissu glandulaire est discuté en fonction des observations réalisées dans d'autres cellules stéroïdogènes à reticulum abondant. La signification des deux aspects cellulaires observés dans l'interrénale est discutée en relation avec les résultats expérimentaux obtenus en particulier chez le rat.Cette étude révèle que les critères d'activité d'une cellule stéroïdogène sont délicats à établir et doivent être différents d'un tissu à l'autre.

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Tissues secreting steroid hormones in urodele amphibians

Summary The fine structure of testis glandular tissue and interrenal gland cells of Pleurodeles shows the general features observed in other steroïdogenic cells. Certain differences exist between the two tissues. The agranular endoplasmic reticulum of the glandular tissue cells is well developed and present in all cells of similar appearance. On the contrary, the interrenal tissue cells show two different features. The first is characterised by a poorly developed smooth endoplasmic reticulum, compared with that of the glandular tissue, by small and numerous mitochondria, and finally by small electron dense lipid droplets. The second feature is the small number of mitochondria often giant and with fascicles of straight tubular cristae and numerous large lipid droplets of low electron density.The effect of hypophysectomy on the glandular tissue cells seem very slight. The endoplasmic reticulum and the 5-3 -hydroxysteroid dehydrogenase activity persists for several months. In the interrenal tissue, the proportions of the two different cellular features are modified. Cells rich in lipids and with large mitochondria are more abundant. It is possible to demonstrate a 5-3 -hydroxysteroid dehydrogenase activity for a long time after hypophysectomy. The functional significance of the agranular endoplasmic reticulum is discussed in relation to some other observations on different steroidogenic cells with a well developed agranular endoplasmic reticulum. The significance of the two cellular features observed in the interrenal gland is discussed in connection with experimental data obtained in the frog and the rat.This study shows that it is difficult to define criteria of cellular activity, which probably differ from one tissue to another.

Equipe de Recherche associée au C. N. R. S. Cytologie Ultrastructurale n 129.     

Patterns of cellular proliferation and migration in the developing tectum mesencephali of the frog Rana temporaria and the salamander Pleurodeles waltl

The development of the tectum mesencephali was studied in the frog Rana temporaria and the salamander Pleurodeles waltl by means of nuclear staining and by labeling of cells with bromodeoxyuridine (BrdU). The general spatial and temporal pattern of cell proliferation and cell migration is the same in both species, despite drastic differences in overall tectal morphology. However, the salamander species differs from the frog species by (1) a generally lower cell proliferation rate, (2) a reduction in the activity of the lateral proliferation zone, and (3) a reduction in the formation of superficial cellular layers. Because point (3) affects processes that occur late in ontogeny, our experiments provide evidence that the simple morphology of the tectum of Pleurodeles waltl, compared with the multilayered tectum of Rana, is a consequence of a paedomorphic alteration of the ancestral developmental pattern of the amphibian tectum.     

Noradrenergic and adrenergic systems in the brain of the urodele amphibian,Pleurodeles waltlii,as revealed by immunohistochemical methods

The distribution of noradrenaline and adrenaline in the brain of the urodele amphibian Pleurodeles waltlii has been studied with antibodies raised against noradrenaline and the enzymes dopamine--hydroxylase and phenylethanolamine-N-methyltransferase. Noradrenaline-containing cell bodies were found in the anterior preoptic area, the hypothalamic nucleus of the periventricular organ, the locus coeruleus and in the solitary tract/area postrema complex at the level of the obex. Noradrenergic fibers are widely distributed throughout the brain innervating particularly the ventrolateral forebrain, the medial amygdala, the lateral part of the posterior tubercle, the parabrachial region and the ventrolateral rhombencephalic tegmentum. Putative adrenergic cell bodies were found immediately rostral to the obex, ventral to the solitary tract. Whereas the cell bodies and their dendrites were Golgi-like stained, axons were more difficult to trace. Nevertheless, some weakly immunoreactive fibers could be traced to the basal forebrain. A comparison of these results with data previously obtained in anurans reveals not only several general features, but also some remarkable species differences.Abbreviations Acc Nucleus accumbens - AP area postrema - Apl amygdala, pars lateralis - Apm amygdala, pars medialis - ca commissura anterior - Cb cerebellum - cc central canal - Dp dorsal pallium - epl external plexiform layer - gl glomerular layer of the olfactory bulb - H ganglion habenulae - igl internal granular layer - Ip nucleus interpeduncularis - Lc locus coeruleus - Ll lateral line lobe - Lp lateral pallium - Ls lateral septum - ml mitral cell layer - Mp medial pallium - Ms medial septum - nPT nucleus pretectalis - NPv nucleus of the periventricular organ - nV nervus trigeminus - oc optic chiasm - Poa preoptic area - Ri nucleus reticularis inferior - SC nucleus suprachiasmaticus - sol solitary tract - Str striatum - thd thalamus dorsalis - thv thalamus ventralis - To tectum opticum - TP tuberculum posterius - V ventricle - VH ventral hypothalamic nucleus - III nucleus nervi oculomotorii - IXm nucleus motorius nervi glossopharyngei - Xm nucleus motorius nervi vagi     

History of West Mediterranean newts,Pleurodeles (Amphibia: Salamandridae), inferred from old and recent DNA sequences

MtDNA sequences (396 bp cytochrome b and 369 bp 12S rRNA) from recent material and old museum specimens indicate Pleurodeles poireti and P. waltl form independent clades with 7.76% genetic divergence. Within P. poireti, populations from Djebel Edough, NE Algeria are very distinct with 6.12% genetic divergence from the remainder and may deserve separate species status. Away from Djebel Edough, P. poireti consists of three distinct clades (coastal NW Tunisia; central N Algeria; Constantine plus inland NW Tunisia) with a maximum genetic divergence of only 1%. P. waltl contains two clades with 2.96% genetic divergence, one in SE and E Spain plus north Morocco, the other in Portugal and SW and central Spain. Pleurodeles probably invaded NW Africa from SW Europe during the Messinian Salinity Crisis, when land contact was first established at 5.6 Ma, and then interrupted at 5.3 Ma. Molecular clocks, calibrated in the assumption that the latter event separated P. waltl and P. poireti, suggest that Pleurodeles diverged from its sister taxon, Tylototriton, at about 8.6–10 Ma. Djebel Edough P. poireti separated at about 4.2 Ma, perhaps through isolation on a temporary, now ‘fossil’, island initiated by the Messinian crisis. Differentiation in remaining P. poireti may have been caused by Pleistocene climatic fluctuations, while bifurcation in P. waltl appears to have taken place in the Pliocene approximately between 3.2 and 2 Ma. This species reached Morocco very recently, perhaps as a result of human introduction. Use in Pleurodeles of the slower divergence rates estimated in some other salamandrids results in a less parsimonious historical hypothesis that does not fit known geophysical events.     

Les éléments cytoplasmiques au cours de la spermiogenèse du TritonPleurodeles waltlii Michah

Résumé L'origine et la morphogenèse des différents éléments de l'acrosome du spermatozode dePleurodeles waltlii ont été suivies et décrites depuis le tout début de la spermiogenèse. La formation de la vésicule acrosomienne et son évolution en une coiffe acrosomienne se fait selon le schéma classique. Son extrémité apicale se différencie tardivement en un bouton terminal et un crochet. Les trois parties de la coiffe diffèrent dans leur composition et leur structure fine.Les volumineux et complexes éléments situés sous la coiffe acrosomienne: axe, baguette puis manchon périphérique et manchon moyen, sont dépourvus de polysaccharides. Leur origine est envisagées. Ils sont comparés aux éléments situés dans l'espace sous-acrosomien des spermatozodes des autres vertébrés.

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The cytoplasmic elements during spermiogenesis in the triturusPleurodeles waltlii MichahI. Acrosome genesis

Summary The origin and the morphogenesis of the acrosome different parts ofPleurodeles spermatozoon, have been investigated and described from the early beginning spermiogenesis process. The acrosomal vesicle and acrosomal cap formation take place according to the classical scheme. The acrosomal anterior tip cap late differentiate in a blunt terminal knob and a hook. The three cap parts differ in their composition and fine structure.The large and complicated structure stretching under the acrosomal cap: axis, peripheral muff and middle muff, are devoided of polysaccharides; their origin is discussed. They are compared with the subacrosomal components lying in the other vertebrates spermatozoon subacrosomal space.

Equipe de Recherche Associée au C.N.R.S., E.R.A. n^o 129.     

Regulation of endogenous Ca2+ channels by cyclic AMP and cyclic GMP-dependent protein kinases in Pleurodeles oocytes

The effects of cyclic AMP (cAMP) and cyclic GMP (cGMP) on dihydropyridine sensitive Ca2+ channels were investigated under voltage-clamp in defolliculated Pleurodeles oocytes. Intracellular injection of cAMP or extracellular application of the permeable cAMP analogue (8-Bromo cAMP, 8Br-cAMP) decreased the Ba current (IBa). This effect on IBa was blocked by the injection of protein kinase A inhibitor. Similar results were found upon internal application of the catalytic subunit of protein kinase A. In contrast, the injection of cGMP or perfusion of 8Br-cGMP increased IBa amplitude. The increase of IBa by 8Br-cGMP was blocked by the injection of the selective inhibitor of protein kinase G (KT5823).These results support the hypothesis that the basal Ba current amplitude of Pleurodeles oocytes is under the control of Protein Kinases A (PKA) and G (PKG) activity.This regulation of Ca2+ channels by the second messengers, and particularly by cAMP may reflect an important step in the maturation processus of Pleurodeles oocytes.     

Immunolocalization of a nuclear protein bound to the sphere organelle during oogenesis and embryogenesis inPleurodeles waltl

Summary The distribution of a nuclear antigen ofPleurodeles waltl oocytes, recognized by the monoclonal antibody B24/1, has been studied during oogenesis and early embryonic development. In stage I oocytes the antigen was localized in the nucleoplasm and on two atypical structures of lampbrush chromosomes, the spheres (S) and the mass (M). The immunostaining increased as the oocyte developed. In stage VI oocytes, the nucleoplasm and spheres showed intense staining. At this stage, the nucleoplasm often contained free spheres which were also labelled. The staining of M diminished during oogenesis, as did its size. Immunoblots of nuclear proteins of oocytes at different stages confirmed that there was an accumulation of this protein during oogenesis. During embryonic development, the nuclei of all the cells of blastula and gastrula were labelled by this antibody: there was no embryonic regionalization. Starting from the neurula stage, the staining progressively disappeared from the nuclei of ectodermal and mesodermal cells. In the tailbud stage, only the endodermal cell nuclei showed faint staining. Immunoblots of proteins from embryos of different stages showed that the quantity of this protein was constant until the young gastrula stage and then decreased progressively; in the young tailbud stage, this protein was practically absent. B24/1 is the first described protein of the sphere. This protein is accumulated in the oocyte nucleus and behaves like a maternal polypeptide, shifting early in the nuclei during embryonic development. Thus, B24/1 probably has a function required from the early developmental stages, perhaps in relation with small nuclear ribonucleoproteins.     

Distribution of NCAM-180 and polysialic acid in the developing tectum mesencephali of the frog Discoglossus pictus and the salamander Pleurodeles waltl

The 180 kDa component of the neural cell adhesion molecule (NCAM-180), total NCAM (NCAM-total) and the polysialic acid modification of NCAM (PSA) show similar temporal and spatial regulation in the developing tecta of Pleurodeles waltl (salamander) and Discoglossus pictus (frog). Whereas NCAM-total is found throughout the tectal tissue on neurons and glia, NCAM-180 is only found on nonproliferating neurons and in fiber layers. PSA is expressed by a subset of NCAM-180-positive cells. Western blots show that there is little polysialylated NCAM-140 in the developing amphibian tectum. Regions unstained for PSA and NCAM-180 correspond precisely to the growth zones of the tectum. NCAM-180 and PSA are not present in tecta of early larvae. Staining intensity is strongest at midlarval stages for both antigens. At metamorphosis, PSA is strongly downregulated, whereas NCAM-180 is downregulated in juvenile animals. Both antigens are still present in fiber layers of adult animals. In dissociated tissue culture of the frog tectum, NCAM-180 is not present on astrocytes, but on neuronal cells. Expression is enhanced at cell contact sites, suggesting that NCAM-180 is involved in cell contact stabilization. This study shows that general features of temporal and spatial regulation of NCAM isoforms and PSA are highly conserved in frog and salamander tecta, despite large differences in the rate of cell migration and the degree of lamination in these homologous brain regions.     

Morphological,histochemical, and ultrastructural characterization of the accessory cells of neuromasts in the salamander Pleurodeles waltlii

Summary The ultrastructural and histochemical features of the accessory cells of the neuromast of the salamander P. waltlii have been examined. Three types of accessory cells, supporting, mantle, and basal, were found, but only the first 2 are considered in this article. Supporting cells characterized by a highly dilated endoplasmic reticulum occur among and surrounding sensory cells. Mantle cells, morphologically different from the supporting cells, surround the remainder of the neuromast. Both types of accessory cells exhibit histochemically different secretory materials. Our morphological results suggest that both accessory cells contribute to the formation of cupular material.