scholarly journals Developmental reorganization of the skeletal framework and its surface lamina in fusing muscle cells.

1981 ◽  
Vol 91 (1) ◽  
pp. 103-112 ◽  
Author(s):  
A B Fulton ◽  
J Prives ◽  
S R Farmer ◽  
S Penman

The skeletal framework of cells, composed of internal structural fibers, microtrabeculae, and the surface lamina, is revealed with great clarity after extraction with detergent. When muscle cells fuse to form a multinucleated myotube, their skeletal framework reorganizes extensively. When myoblasts prepare to fuse, the previously continuous surface lamina develops numerous lacunae unique to this stage. The retention of iodinated surface proteins suggests that the lacunae are not formed by the extraction of lamina proteins. The lacunae appear to correspond to extensive patches that do not bind concanavalin A and are probably regions of lipid bilayer devoid of glycoproteins. The lacunae appear to be related to fusion and disappear rapidly after the multinucleated myotube is formed. When muscle cells fuse, their internal structural networks must interconnect to form the framework of the myotube. Transmission electron microscopy of skeletal framework whole mounts shows that proliferating myoblasts have well developed and highly interconnected internal networks. Immediately before fusion, these networks are extensively reorganized and destabilized. After fusion, a stable, extensively cross-linked internal structure is reformed, but with a morphology characteristic of the myotube. Muscle cells therefore undergo extensive reorganization both on the surface and internally at the time of fusion.

1996 ◽  
Vol 44 (1) ◽  
pp. 69
Author(s):  
LRG Cannon ◽  
NA Warson

Temnocephala minor Haswell, 1888 lives ectosymbiotically on the surface of the freshwater crayfish Cherax destructor in the Murray-Darling drainages of Australia. Some glands open on the postero-lateral margin and, being moderately refractory to many stains, can be overlooked in whole mounts and sections, and were, in fact, missed by Haswell. Observations were made on living worms with intra vitam dyes, and on whole mounts, wax sections and ultrathin sections using transmission electron microscopy (TEM) to characterise the secretion from these glands and ascertain its mode of manufacture. The function of the glands remains unknown although it appears non-adhesive.


2006 ◽  
Vol 74 (4) ◽  
pp. 2453-2456 ◽  
Author(s):  
Julianna LeMieux ◽  
David L. Hava ◽  
Alan Basset ◽  
Andrew Camilli

ABSTRACT The rlrA pathogenicity islet in Streptococcus pneumoniae TIGR4 encodes three surface proteins, RrgA, RrgB, and RrgC, and three sortase enzymes. Using transmission electron microscopy, cell fractionation, cell wall sorting signal domain swapping, and Western blotting, we show that RrgA and RrgB are incorporated into a multisubunit pilus in S. pneumoniae.


Development ◽  
1985 ◽  
Vol 88 (1) ◽  
pp. 1-13
Author(s):  
Kensuke E. Nakano ◽  
Harukazu Nakamura

The aim of the present study was to elucidate the origin of the striated muscle cells in the avian iris. For this purpose we adopted interspecific transplantation between quail and chick embryos because quail cells can be used as biological markers in this system. We transplanted isotopically and isochronically (6- to 7-somite stage) a fragment of a dorsal part of the quail neural anlage into a chick embryo at the level corresponding to the posterior prosencephalon and the mesencephalon on the right-hand side. In the chimaeric embryo, the iris epithelium comprised host chick cells, while most of the stromal cells of the iris on the operated side possessed the quail nuclear marker. At 19 days after the operation, the striated muscle cells had differentiated in the chimaeric embryo. These cells, as well as connective tissue cells and the Schwann cells of the iris of the chimaera, were shown to possess typical quail nuclei by light and transmission electron microscopy. From these findings, we conclude that the striated muscle cells originate from the neural crest.


1979 ◽  
Vol 36 (1) ◽  
pp. 97-107
Author(s):  
W.D. Cohen ◽  
N.B. Terwilliger

The elliptical, anucleate erythrocytes of camels have been examined for the presence of marginal bands and their constituent microtubules. Lysis of erythrocytes under microtubule-stabilizing conditions readily revealed marginal bands in at least 3 % of the cells, as observed by phase-contrast and darkfield light microscopy. Microtubules plus a marginal band-encompassing network of material are visible in lysed cell whole mounts with transmission electron microscopy. Marginal band microtubules are also evident in electron micrographs of thin-sectioned camel erythrocytes identifiable as reticuloyctes on the basis of submaximal electron density (reduced haemoglobin iron content) and presence of polysomes. The results suggest that marginal bands may be involved in morphogenesis of camel erythrocytes but are not required for maintenance of their ellipticity after cells are fully differentiated.


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