scholarly journals A freeze-fracture study on the developing satellite cells of spinal ganglia in the chick embryo

1988 ◽  
Vol 46 (1) ◽  
pp. 6-9
Author(s):  
Claudio A. Ferraz de Carvalho ◽  
Ciro F. da Silva
Keyword(s):  
Chick Embryo ◽  
Gap Junctions ◽  
Tight Junctions ◽  
Small Groups ◽  
Satellite Cells ◽  
Freeze Fracture ◽  
Fracture Analysis ◽  
Spinal Ganglia ◽  
Pinocytotic Vesicles ◽  
Fracture Study

A freeze-fracture analysis of the satellite cells of spinal ganglia of the chick embryo was performed in 8 successive stages of development, from the 5th incubation day to hatching. The characteristic laminar disposition of the cells were first observed on the 7th day. Tight junctions were found at the 20th incubation day. Small groups or irregular aggregates of particles, but not gap junctions, were described on the 7th and 8th days. Pinocytotic vesicles were pointed out in the different stages considered.

Tight and gap junctions in the intestinal tract of tunicates (Urochordata): a freeze-fracture study

1986 ◽  
Vol 84 (1) ◽  
pp. 1-17
Author(s):  
N.J. Lane ◽  
R. Dallai ◽  
P. Burighel ◽  
G.B. Martinucci
Keyword(s):  
Gap Junctions ◽  
Tight Junctions ◽  
Thin Section ◽  
Intestinal Tract ◽  
Freeze Fracture ◽  
Intestinal Cells ◽  
Fracture Profile ◽  
Tracer Studies ◽  
Septate Junctions ◽  
Fracture Study

The intestinal tracts from seven different species of tunicates, some solitary, some colonial, were studied fine-structurally by freeze-fracture. These urochordates occupy an intermediate position phylogenetically between the vertebrates and the invertebrates. The various regions of their gut were isolated for examination and the junctional characteristics of each part investigated. All the species examined exhibited unequivocal vertebrate-like belts of tight-junctional networks at the luminal border of their intestinal cells. No septate junctions were observed. The tight junctions varied in the number of their component strands and the depth to which they extended basally, some becoming loose and fragmented towards that border. The junctions consisted of ridges or rows of intramembranous particles (IMPs) on the P face, with complementary, but offset, E face grooves into which IMPs sometimes fractured. Tracer studies show that punctate appositions, the thin-section correlate of these ridge/groove systems, are sites beyond which exogenous molecules do not penetrate. These junctions are therefore likely to represent permeability barriers as in the gut tract of higher chordates. Associated with these occluding zonular junctions are intermediate junctions, which exhibit no identifiable freeze-fracture profile, and macular gap junctions, characterized by a reduced intercellular cleft in thin section and by clustered arrays of P face particles in freeze-fractured replicas; these display complementary aggregates of E face pits. The diameters of these maculae are rarely very large, but in certain species (for example, Ciona), they are unusually small. In some tissues, notably those of Diplosoma and Botryllus, they are all of rather similar size, but very numerous. In yet others, such as Molgula, they are polygonal with angular outlines, as might be indicative of the uncoupled state. In many attributes, these various junctions are more similar to those found in the tissues of vertebrates, than to those in the invertebrates, which the adult zooid forms of these lowly chordates resemble anatomically.

scholarly journals VARIATIONS IN TIGHT AND GAP JUNCTIONS IN MAMMALIAN TISSUES

1972 ◽  
Vol 53 (3) ◽  
pp. 758-776 ◽  
Author(s):  
Daniel S. Friend ◽  
Norton B. Gilula
Keyword(s):  
Smooth Muscle ◽  
Gap Junctions ◽  
Tight Junctions ◽  
Adrenal Cortex ◽  
Freeze Fracture ◽  
Junctional Complex ◽  
Exocrine Glands ◽  
Rat Pancreas ◽  
Zonula Occludens ◽  
Mammalian Tissues

The fine structure and distribution of tight (zonula occludens) and gap junctions in epithelia of the rat pancreas, liver, adrenal cortex, epididymis, and duodenum, and in smooth muscle were examined in paraformaldehyde-glutaraldehyde-fixed, tracer-permeated (K-pyroantimonate and lanthanum), and freeze-fractured tissue preparations. While many pentalaminar and septilaminar foci seen in thin-section and tracer preparations can be recognized as corresponding to well-characterized freeze-fracture images of tight and gap junction membrane modifications, many others cannot be unequivocally categorized—nor can all freeze-etched aggregates of membrane particles. Generally, epithelia of exocrine glands (pancreas and liver) have moderate-sized tight junctions and large gap junctions, with many of their gap junctions basal to the junctional complex. In contrast, the adrenal cortex, a ductless gland, may not have a tight junction but does possess large gap junctions. Mucosal epithelia (epididymis and intestine) have extensive tight junctions, but their gap junctions are not as well developed as those of glandular tissue. Smooth muscle contains numerous small gap junctions The incidence, size, and configuration of the junctions we observed correlate well with the known functions of the junctions and of the tissues where they are found.

Morphological Changes of Intercellular Junctions in the Rat Submandibular Gland Treated by Long-term Repeated Administration of Isoproterenol

1987 ◽  
Vol 66 (8) ◽  
pp. 1303-1309 ◽  
Author(s):  
T. Inoue ◽  
H. Yamane ◽  
T. Yamamura ◽  
M. Shimono
Keyword(s):  
Gap Junctions ◽  
Tight Junctions ◽  
Morphological Changes ◽  
Freeze Fracture ◽  
Acinar Cells ◽  
Intercellular Junctions ◽  
Repeated Administration ◽  
Experimental Conditions ◽  
Significant Difference

Long-term repeated administration of isoproterenol (lPR) 2 mg/100 g bw, once daily for ten days, resulted in morphological changes in the intercellular junctions of rat submandibular glands, which were investigated by means of the freeze fracture technique. A significantly increased number of tight-junctional strands was present. These junctional strands extended much deeper toward the basal membrane than those in normal acinar cells. The basal frontier strands that branched from the networks of tight junctions were elongated and had either free-endings or terminal loops, which were more frequently observed in the IPR-treated acinar cells than in untreated acinar cells. Some of the strands of tight junctions were connected to small gap junctions. The diameters of gap junctions were not significantly different from those of control acinar cells. However, smooth areas devoid of particles were found intermingling with the usual packed particles in irregularly shaped small gap junctions. There was no significant difference between the desmosomes of IPR-treated and untreated acinar cells, in terms of either morphology or distribution. These changes in junctional morphology in the IPR-treated acinar cells resemble those seen in salivary glands during development, and in some experimental conditions including tumorous changes.

Homocellular and heterocellular gap junctions in Limulus: A thin-section and freeze-fracture study

1973 ◽  
Vol 43 (3-4) ◽  
pp. 298-312 ◽  
Author(s):  
Ross G. Johnson ◽  
William S. Herman ◽  
Doris M. Preus
Keyword(s):  
Gap Junctions ◽  
Thin Section ◽  
Freeze Fracture ◽  
Fracture Study

scholarly journals Tight-junctional strands first appear in regions where three cells meet in differentiating olfactory epithelium: a freeze-fracture study

1988 ◽  
Vol 89 (4) ◽  
pp. 495-505
Author(s):  
B.P. Menco
Keyword(s):  
Embryonic Development ◽  
Gap Junction ◽  
Tight Junctions ◽  
Olfactory Epithelium ◽  
Freeze Fracture ◽  
Subsequent Development ◽  
Epithelial Surface ◽  
Direction Parallel ◽  
Longitudinal Orientation ◽  
Fracture Study

Tight junctions of the olfactory epithelium of rat embryos were studied at the 14th day of gestation and during their subsequent development. Two different epithelial morphologies could be distinguished at the 14th gestational day. In one group of embryos the epithelial surface appeared undifferentiated, with tight-junctional strands found exclusively in regions where three cells met. The main orientation of these strands is in a direction parallel to the longitudinal orientation of the epithelial cells. These junctions resemble tight junctions that interconnect three cells, i.e. tricellular tight junctions, in that respect. However, unlike these the junctions mainly have single strands of particles, whereas tricellular junctions usually consist of paired strands of particles. Tight-junctional strands were completely absent in areas where two cells met. These areas, i.e. those of incipient bicellular tight junctions, had gap-junction-like aggregates of intramembranous particles. Another group of 14-day-old embryos displayed a differentiating olfactory epithelial surface with bicellular as well as tricellular tight-junctional strands. The latter ones were paired. Here too the tight-junctional belts displayed some gap-junction-like aggregates of particles, but there were considerably fewer of these than earlier. As one or the other tight-junctional appearance was always seen in a single freeze-fracture replica, it is reasonable to assume that the two tight-junctional appearances reflect a sequential pattern of differentiation peculiar to the whole surface of the olfactory epithelium, i.e. to surfaces of receptor cells as well as to surfaces of supporting cells. It would appear that, at the onset of olfactory epithelial differentiation, tight junctions first interconnect cells in regions where three cells meet and that tricellular strand formation precedes the formation of bicellular strands. When strands were present at the 14th day of embryonic development, their numbers were lower than those found later. However, strand packing, expressed as the density per micrometre of strands parallel to the epithelial surface, increased beginning at the 16th day of embryonic development.

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