CONTENT - International Society of Zoological Sciences
CONTENT - International Society of Zoological Sciences
CONTENT - International Society of Zoological Sciences
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ICZ2008 – Abstracts S23<br />
Comparative studies on egg capsules ultrastructure in two<br />
species <strong>of</strong> Tardigrada: Dactylobiotus dispar Murray, 1907 and<br />
Isohypsibius granulifer Thulin, 1928.<br />
Izabela Poprawa and Magdalena Rost-Roszkowska<br />
Department <strong>of</strong> Animal Histology and Embryology, University <strong>of</strong><br />
Silesia, Bankowa 9, 40-007 Katowice, Poland<br />
The eggs <strong>of</strong> Dactylobiotus dispar and Isohypsibius granulifer,<br />
similar to other Tardigrada eggs (Węglarska 1982), are covered<br />
with two shells: the vitelline envelope and the chorion. In both<br />
cases the vitelline envelope is very thin but the chorion has a<br />
multilayered structure. In both analyzed species the chorion is<br />
composed <strong>of</strong> 3 layers: (1) the inner layer <strong>of</strong> medium electron<br />
density; (2) middle, labyrinthine layer; (3) the outer layer <strong>of</strong><br />
medium electron density. Differences between those two species<br />
are connected with all layers thickness and the structure <strong>of</strong><br />
chorion’s surface.<br />
The labyrinthine layer <strong>of</strong> D. dispar is thinner than the same layer in<br />
the chorion <strong>of</strong> I. granulifer whereas the outer layer is thicker than<br />
the outer one <strong>of</strong> I. granulifer. The chorion surface <strong>of</strong> D. dispar is<br />
covered with small, conical processes with hooked tips. Such<br />
processes are not observed on the surface <strong>of</strong> L. granulifer eggs.<br />
Both egg capsules do not possess micropylar opening.<br />
Węglarska B. (1982) Ultrastructural study <strong>of</strong> the formation <strong>of</strong> egg<br />
envelops in Macrobiotus richtersi (Eutardigrada). In. Nelson D.R.<br />
(ed.) Proceedings <strong>of</strong> the third international symposium on the<br />
Tardigrada. East Tennessee State University Press, pp. 115-128.<br />
Extracellular vacuoles in developing midgut epithelium <strong>of</strong><br />
Melasoma saliceti (Chrysomelidae, Coleoptera) embryos<br />
Magdalena Rost-Roszkowska and Jerzy Klag<br />
Department <strong>of</strong> Animal Histology and Embryology, University <strong>of</strong><br />
Silesia, Bankowa 9, 40-007 Katowice, Poland<br />
Embryonic development <strong>of</strong> Melasoma saliceti lasts 7 days in 22 0 C.<br />
Stomodaeum and proctodaeum invaginate at the anterior and<br />
posterior ends <strong>of</strong> the germ band. Together with the ectodermal<br />
tissue the endoderm cells also enter into the embryo. The<br />
endoderm cells start to migrate over the yolk mass as two lateral<br />
bands <strong>of</strong> cells. On the fifth day <strong>of</strong> development the endoderm cells<br />
spread over the ventral and dorsal sides <strong>of</strong> the yolk and form the<br />
single layered primordium <strong>of</strong> the midgut epithelium whose cells<br />
become connected by specialised intercellular junctions <strong>of</strong> zonula<br />
adherens type. At the same time, between the cells, the<br />
intercellular spaces widen in some places. Initially the wide<br />
intercellular spaces have irregular outlines, but later they widen,<br />
acquire spherical shapes and transform into peculiar extracellular<br />
vacuoles. Each vacuole is enclosed within a band <strong>of</strong> junctional<br />
complex. The complexes are formed by zonula adherens, septate<br />
and gap junctions. On the sixth day <strong>of</strong> development the<br />
endodermal epithelium cells change shape from flat to cuboidal<br />
and eventually into columnar. At the same time, the vacuoles grow<br />
and become filled with electron dense content. The cell<br />
membranes enclosing the vacuoles form long, densely spaced<br />
microvilli eventually filling the vacuole completely. At the beginning<br />
<strong>of</strong> seventh day <strong>of</strong> development the apical surfaces <strong>of</strong> the<br />
embryonic midgut cells are completely smooth but the extracellular<br />
vacuoles come close to the midgut surface. At the end <strong>of</strong> the<br />
seventh day, shortly before hatching the extracellular vacuoles<br />
open to the midgut lumen and the microvilli spread over the apical<br />
surfaces <strong>of</strong> the midgut epithelium. Thus in very short time larval<br />
midgut, completely covered with fully formed brush-border is<br />
formed. The epithelial cells remain connected by zonulae<br />
adherentes continuous junctions and gap junctions. The septate<br />
junctions are seen only sporadically. The above-presented way <strong>of</strong><br />
embryonic “preformation” <strong>of</strong> larval midgut microvilli in a<br />
holometobolous insect has not been described. Similar<br />
phenomenon <strong>of</strong> microvilli preformation was observed during<br />
differentiation <strong>of</strong> regenerative cells in some insect species.<br />
- 95 -<br />
Fine structure <strong>of</strong> the midgut epithelium <strong>of</strong> two species<br />
belonging to Archaeognatha Lepismachilis notata and<br />
Machilis hrabei (Insecta)<br />
Magdalena Rost-Roszkowska 1 and Jitka Vilimova 2<br />
1 Department <strong>of</strong> Animal Histology and Embryology, University <strong>of</strong><br />
Silesia, Bankowa 9, 40-007 Katowice, Poland<br />
2 Charles University, Faculty <strong>of</strong> Science, Department <strong>of</strong> Zoology,<br />
128 44 Praha 2, Vinicna 7, Czech Republic<br />
Two primitive wingless insect taxa Archaeognatha and Zygentoma<br />
have originally formed one order Thysanura. Later, they were<br />
distinguished as two distinct orders Archaeognatha and<br />
Zygentoma, the basal taxa <strong>of</strong> Insecta. Recently some authors have<br />
suggested a recovery <strong>of</strong> the order Thysanura, thus the<br />
classification and relationship <strong>of</strong> Archaeognatha and Zygentoma<br />
are not still completely resolved. We analyzed the midgut<br />
epithelium and processes <strong>of</strong> its degeneration and regeneration in<br />
Thermobia domestica and Lepisma saccharina, which belong to<br />
Zygentoma (Rost 2006). In our present studies we compare the<br />
ultrastructure <strong>of</strong> the midgut epithelium in Lepismachilis notata and<br />
Machilis hrabei (Archeognatha) with those <strong>of</strong> Zygentoma.<br />
Midgut epithelium <strong>of</strong> both archaeognathans Lepismachilis notata<br />
and Machilis hrabei is composed <strong>of</strong> columnar epithelial cells and<br />
regenerative cells, which form regenerative cell groups. In both<br />
analyzed species the midgut epithelium resembles that <strong>of</strong> T.<br />
domestica and L. saccharina (Zygentoma). The cytoplasm <strong>of</strong> the<br />
epithelial cells shows distinct regionalization in arrangement <strong>of</strong><br />
organelles, so basal, perinuclear and apical regions are<br />
distinguished. The cytoplasm <strong>of</strong> the regenerative cells is poor in<br />
organelles. They are capable <strong>of</strong> intensive proliferation and<br />
differentiation in epithelial ones. The first sign <strong>of</strong> their differentiation<br />
is appearance <strong>of</strong> cisterns <strong>of</strong> RER and SER, and numerous<br />
mitochondria in their cytoplasm.<br />
Rost M.M. 2006. Comparative studies on regeneration <strong>of</strong> the<br />
midgut epithelium in Lepisma saccharina L. and Thermobia<br />
domestica Packard (Insecta; Zygentoma). Annals <strong>of</strong> Entomological<br />
<strong>Society</strong> <strong>of</strong> America 99: 910-916.<br />
Molecular construction <strong>of</strong> tissues and organs <strong>of</strong> the Ciona<br />
intestinalis larva<br />
Nori Satoh<br />
Department <strong>of</strong> Zoology, Graduate School <strong>of</strong> Science, Kyoto<br />
University, Kyoto 606-8502, Japan<br />
Ascidians, or sea squirts, are sessile marine invertebrate<br />
chordates. Although the adult is a filter feeder, the fertilized egg<br />
develops quickly into so-called tadpole larva. The larva is<br />
composed <strong>of</strong> only ~2600 cells, which constitute a small number <strong>of</strong><br />
organs including epidermis, central nervous system (CNS),<br />
endoderm and mesenchyme in the trunk, and notochord and<br />
muscle in the tail. This represents the most simplified chordate<br />
body plan. Specification <strong>of</strong> ascidian embryonic cells takes place<br />
very early at the cleavage stage; developmental fates <strong>of</strong> epidermis,<br />
CNS, endoderm, notochord and muscle are restricted by the 110cell<br />
stage. Together with well-characterized lineage <strong>of</strong> embryonic<br />
cells, the ascidian embryo may provide an appropriate<br />
experimental system to explore genome-widely the genetic<br />
cascades underlying embryonic cell specification. The draft<br />
genome <strong>of</strong> Ciona intestinalis has been decoded in 2002, and its<br />
~120 Mbp euchromatic genome contains ~16,000 protein-coding<br />
genes. Among these is a fundamental set <strong>of</strong> conserved chordate<br />
genes encoding transcriptional factors and cell signaling molecules.<br />
A thorough examination <strong>of</strong> Ciona gene expression (the<br />
transcriptome) is ongoing, including large-scale EST analyses<br />
(~700,000 ESTs), cDNA sequencing, in situ hybridization, and<br />
microarray analyses. All <strong>of</strong> the information is now available with a<br />
new Web site <strong>of</strong> our lab. Here we wish to discuss our current<br />
approach using transgenic lines and microarray to disclose genes<br />
involved in the formation <strong>of</strong> the notochord, central nervous system,<br />
and muscle <strong>of</strong> the Ciona larva.