The distribution of the neural fat body sheath and the accessibility of the extraneural space in the stick insect, carausius morosus

1971 ◽  
Vol 3 (4) ◽  
pp. 589-603 ◽  
Author(s):  
N.J. Lane ◽  
J.E. Treherne
1972 ◽  
Vol 56 (1) ◽  
pp. 129-137
Author(s):  
J. E. TREHERNE

1. The effects of variation in the sodium concentration of the bathing media on axonal function has been measured in de-sheathed connectives in the presence of the overlying neural fat-body sheath. 2. The response to solutions of the same sodium concentration as the haemolymph (15 mM/1) was found to be essentially similar to that recorded in de-sheathed connectives in the absence of the fat-body sheath, there being a rapid decline in amplitude of the recorded action potentials in both preparations. 3. On the basis of these observations it is concluded that the neural fat-body sheath is unlikely to be involved in the regulation of the extra-neuronal sodium level.


1980 ◽  
Vol 46 (1) ◽  
pp. 1-16
Author(s):  
F. Giorgi ◽  
F. Macchi

Vitellogenesis in the stick insect Carausius morosus (Br.) has been studied with the goal of identifying vitellogenin in various tissues. Following exposure to in vivo to radioactive amino acids, oocytes in the medium size range are labelled with a minimum delay of 6 h after the time of injection. Incorporation of radioactivity under these conditions is shown to depend upon accumulation of proteins rather than on a differential rate of protein synthesis in succeeding stages of oogenesis. By immunochemical analyses, it is shown that at least two antigens are common to both haemolymph and ovary and that one of these is also present in the fat body. Both antigens are labelled during exposure to radioactive amino acids. When analysed by the SDS polyacrylamide gel electrophoresis, extracts from both haemolymph and ovary appear to share a number of protein fractions which range in molecular weight from 40 000 to 200 000 Daltons. The labelling pattern exhibited by these fractions is clearly indicative of a protein transfer from the fat body to the oocyte. Fat body cultured in vivo for up to 4 h releases a major macromolecular complex in the external medium. The latter has been identified as vitellogenin by both immuno-precipitation assay and SDS polyacrylamide gel electrophoresis. The protein which is synthesized and secreted under these conditions results from the processing of a protein complex of higher molecular weight.


1995 ◽  
Vol 167 (1) ◽  
pp. 379-387 ◽  
Author(s):  
Franco Giorgi ◽  
Antonella Cecchettini ◽  
Maria Teresa Locci ◽  
Massimo Masetti ◽  
James T. Bradley

Micron ◽  
1998 ◽  
Vol 29 (6) ◽  
pp. 451-460 ◽  
Author(s):  
F Giorgi ◽  
A Cecchettini ◽  
A Falleni ◽  
M Masetti ◽  
V Gremigni

Chromosoma ◽  
1980 ◽  
Vol 79 (1) ◽  
pp. 105-114 ◽  
Author(s):  
Laas P. Pijnacker ◽  
Margriet A. Ferwerda

1970 ◽  
Vol 52 (3) ◽  
pp. 653-665 ◽  
Author(s):  
DIANA E. M. PILCHER

1. Urine secretion by isolated Malpighian tubules of Carausius is accelerated by a diuretic hormone which can be extracted from the brain, corpora cardiaca and suboesophageal ganglion. 2. The level of this hormone in the haemolymph varies according to the state of hydration of the insect. 3. The hormone is inactivated by the tubules, and a mechanism is proposed whereby the tubules might be controlled by the hormone in vivo.


1936 ◽  
Vol s2-78 (311) ◽  
pp. 487-511
Author(s):  
A. J. THOMAS

1. The maturation of the egg takes place in the ovarian tube, and is immediately followed by the formation of the cleavagenucleus and its division into many nuclei. 2. The entire products of the cleavage-nucleus migrate to the surface to form the blastoderm. Cleavage of the yolk was not observed even in late stages. Yolk-cells are absent when the blastoderm is being formed. 3. Primitive endodermal cells are proliferated from the middle of the germ-band, and form a membrane between the germ-band and the yolk. The membrane is present only in embryonic stages; some of the cells proliferated wander into the yolk and act as vitellophags. 4. Mesoderm is formed by proliferation of cells from the ventral plate. It is preceded by the formation of a shallow gastrular furrow, and from the bottom of this furrow proliferation takes place. The mesoderm becomes arranged in segmental masses. 5. Two masses of cells proliferated at the anterior and posterior ends of the germ-band are shown to be the endodermal rudiments from which the mid-gut epithelium is formed. The invaginations of the stomodaeum and proctodaeum grow against these masses and carry parts of the proliferating areas near their blind ends. It is shown that the various methods of mid-gut formation which have been described could be reconciled with the process described in Carausius. 6. The hinder end of the mid-gut is flanked by two plates of ectoderm which are forward extensions of the proctodaeum. Into these extensions the Malpighian tubules open, and, as their histology is identical with that of these extensions and widely different from that of the mid-gut, these tubules must be ectodermal in nature. 7. The formation of the amnion and serosa are described.


Sign in / Sign up

Export Citation Format

Share Document