Coaggregation and formation of a joint myocardial tissue by embryonic mammalian and avian heart eel Is

Development ◽  
1980 ◽  
Vol 59 (1) ◽  
pp. 263-279
Author(s):  
Asish C. Nag ◽  
Mei Cheng ◽  
Christopher J. Healy

Intercellular adhesion and tissue reconstruction from homologous dissociated embryonic cells from two species were studied. Dissociated 12-day-old embryonic rat heart cells and 50-h-old embryonic chick heart cells were labeled with tritiated thymidine and allowed to aggregate in Erlenmeyer flasks during rotation culture on a gyratory water-bath shaker. The cultures were continued for 72 h. Cell aggregates were examined microscopically for evidence of contractility and subsequently processed at intervals between 1 and 72 h for transmission electron microscopic autoradiography. Rat and chick hearts used in this study appeared comparable in their stage of development and cellular composition. With the exception of mature blood cells and some fibroblastic non-muscle cells, all chick cardiac muscle cells were labeled with tritiated thymidine. As the cultures continued, aggregates increased in size by continuous accretion of cells and joining of small clusters. The cells within these mixed aggregates exhibited synchronous contractility from 1 h until the cultures were terminated. Most of the aggregation in both control and mixed aggregates was completed within 24 h. Control aggregates consisted of cells from a single species, either chick or rat. Approximately 18 % of labeled chick cardiac muscle cells established intercellular contacts and junctions with unlabeled rat cardiac muscle cells after 6 h of culture. This increased to 72 % after 72 h in culture. The junctions observed between chick and rat cardiac muscle cells were desmosomes and hemidesmosomes. Approximately 13 % of the cardiac muscle cells of one species either chick or rat were found scattered within clusters which contained .15 % of the cells from the other species after 72 h of culture. These scattered cells did not form junctions with monospecific cell groups. The implications of these intercellular adhesions between the same and different species are discussed, bearing two hypotheses in mind: (1) Moscona and collaborators, (2) Burdickand Steinberg. This study suggests that cellular as well as species identity plays an important role in the determination of intercellular adhesion among the embryonic cells from different species.

1970 ◽  
Vol 55 (5) ◽  
pp. 602-619 ◽  
Author(s):  
S. Bosteels ◽  
A. Vleugels ◽  
E. Carmeliet

Permeability of the cardiac cell membrane to choline ions was estimated by measuring radioactive choline influx and efflux in cat ventricular muscle. Maximum values for choline influx in 3.5 and 137 mM choline were respectively 0.56 and 9 pmoles/cm2·sec. In 3.5 mM choline the intracellular choline concentration was raised more than five times above the extracellular concentration after 2 hr of incubation. In 137 mM choline, choline influx corresponded to the combined loss of intracellular Na and K ions. Paper chromatography of muscle extracts indicated that choline was not metabolized to any important degree. The accumulation of intracellular choline rules out the existence of an efficient active pumping mechanism. By measuring simultaneously choline and sucrose exchange, choline efflux was analyzed in an extracellular phase, followed by two intracellular phases: a rapid and a slow one. Efflux corresponding to the rapid phase was estimated at 16–45 pmoles/cm2·sec in 137 mM choline and at 1.3–3.5 pmoles/cm2·sec in 3.5 mM choline; efflux in 3.5 mM choline was proportional to the intracellular choline concentration. The absolute figures for unidirectional efflux were much larger than the net influx values. The data are compared to Na and Li exchange in heart cells. Possible mechanisms for explaining the choline behavior in heart muscle are discussed.


1988 ◽  
Vol 89 (1) ◽  
pp. 97-106
Author(s):  
B.T. Atherton ◽  
M.M. Behnke

The composition and organization of myofibrils at extra-junctional membrane attachment sites in cultured neonatal rat cardiac muscle cells were analysed by immunofluorescence and electron microscopy. When myofibril terminals attached to the cell membrane via focal contacts at regions of the sarcolemma that lacked intercalated discs, they appeared to be non-striated and resembled thick actin cables. Although the non-striated terminals contained actin, myosin and alpha-actinin, the proteins were not organized into recognizable sarcomeres at the light microscopic level. Analysis of the structure of the terminals in the electron microscope confirmed that the usual sarcomeric organization and attachments to the sarcolemma were markedly modified. The non-striated myofibril terminals differed in structure from both stress fibres in non-muscle cells and stress fibre-like structures present in embryonic heart cells in culture. Non-striated myofibril terminals attached to the cell membrane by lateral contact with extra-junctional electron-dense membrane plaques rather than by insertion by their ends into the fascia adherens. It is proposed that the structure and composition of membrane-attachment points for myofibrils may have an influence on the structure, organization or stability of contractile elements in cardiac muscle.


2004 ◽  
Vol 29 (1) ◽  
pp. 83-95 ◽  
Author(s):  
Hung-Chien Wu ◽  
Jaung-Geng Lin ◽  
Chun-Hsien Chu ◽  
Yung-Hsien Chang ◽  
Chung-Gwo Chang ◽  
...  

2005 ◽  
Vol 27 (1) ◽  
pp. 33-51 ◽  
Author(s):  
Ki-Chan Ha ◽  
Han-Jung Chae ◽  
Cheng-Shi Piao ◽  
Suhn-Hee Kim ◽  
Hyung-Ryong Kim ◽  
...  

1981 ◽  
Vol 86 (2) ◽  
pp. 358 ◽  
Author(s):  
M. J. Galvin ◽  
C. A. Hall ◽  
D. I. McRee

2019 ◽  
Vol 174 ◽  
pp. 103-109 ◽  
Author(s):  
Nomin-Erdene Oyunbaatar ◽  
Arunkumar Shanmugasundaram ◽  
Dong-Weon Lee

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