scholarly journals Localization of Wnt8 in the endoplasmic reticulum. Wnt8-HA, which has a dorsalization activity, was injected into a blastomere of an 8-cell-stage Xenopus embryo, and the embryo was fixed 2 hours before stage 10. Immunohistochemistry with anti-HA (left) an

2014 ◽  
Vol 56 (9) ◽  
pp. i-i
1993 ◽  
Vol 160 (1) ◽  
pp. 276-284 ◽  
Author(s):  
Kei Kinoshita ◽  
Tomoko Bessho ◽  
Makoto Asashima
Keyword(s):  

Development ◽  
1985 ◽  
Vol 90 (1) ◽  
pp. 287-309
Author(s):  
Bernard Maro ◽  
Martin H. Johnson ◽  
Susan J. Pickering ◽  
Daniel Louvard

The unfertilized oocyte, fertilized egg and early embryo (2-cell to 16-cell) of the mouse have been examined immunocytochemically for the distribution of antigens associated with the endoplasmic reticulum, the lysosomal and acidic vesicle fraction (100kD antigen), Golgi apparatus (135kD antigen) and coated vesicles (clathrin). The distribution of these antigens has also been examined in isolated 8-cell and 16-cell-stage blastomeres of various ages and phenotypes. Endoplasmic reticulum is detected only weakly in the oocyte and egg, but is seen abundantly at later stages both in association with the nuclear membrane and evenly distributed throughout the cytoplasm, except in regions of cell: cell apposition from which it is excluded. Intracellular clathrin is associated with the spindle in mitotic and meiotic cells. During interphase, clathrin is distributed throughout the cell until the mid-8-cell stage when it is concentrated into the apical region of the cell under the region of membrane at which a surface pole of microvilli will form subsequently. Thus, the cytoplasmic polarization of clathrin precedes overt polarization at the surface. At mitosis, the clathrin relocates to the spindle and is distributed to both daughter cells. It resumes an apical location beneath the surface pole of microvilli in polar daughter 1/16 cells, but remains dispersed in apolar daughter 1/16 cells. Both the lysosomal and Golgi antigens are distributed throughout the cytoplasm until the early 16-cell stage. In pairs of 16-cell blastomeres both antigens aggregate in a single cluster and do so whether the surface phenotype of the blastomeres is polar or apolar. The position of this cluster is not consistently related to the point of contact with the other cell in the pair but there is a suggestion that in cells with a polar surface phenotype the polar foci of Golgi/lysosomal antigens are located between the nucleus and the surface pole at earlier time points, but shift to a position between the basolateral membrane and the nucleus at the later time point. In intact 16-cell embryos also, the aggregated Golgi/lysosomal antigens of polar cells appear to localize to the basal region. The distributions of these various organelles in embryonic cells reported here show a number of differences from those reported previously for mature, differentiated cells.


1977 ◽  
Vol 24 (1) ◽  
pp. 275-294
Author(s):  
S.H. Brawley ◽  
R.S. Quatrano ◽  
R. Wetherbee

Condensation of the chromosomes during the first cell division following fertilization of the brown alga Fucus vesiculosus L. is accompanied by the almost complete disappearance of the nuclear envelope. Golgi vesicles and other small vesicles appear within the spindle, which has paired centrioles at each end. A large amount of rough endoplasmic reticulum is in the surrounding cytoplasm during mitosis, and many vesicles at the spindle margin are encircled by stacks of endoplasmic reticulum. Annulate lamellae are observed during mitosis. The envelope which initially reforms around the chromatin in telophase has unevenly spaced nuclear pores. Cytokinesis results primarily by vesicle addition to a centripetal furrow. Mitochondria and chloroplasts concentrate around the partition site, possibly in association with microfilaments. Fibrillar material is added rapidly to the space between the daughter cells from vesicle discharge of both cells and seems to spread into the older cell wall surrounding the embryo. The rhizoid daughter cell contains numerous mitochondria and hypertrophied Golgi bodies whose vesicles increasingly pack the cell. The thallus daughter cell is packed with a variety of vesicles, and the nucleus is surrounded by many dilated cisternae of rough endoplasmic reticulum. By the four-cell stage, chloroplasts of the rhizoid cells have weakly staining lamellae, while chloroplasts of the thallus cells are actively dividing with deeply staining lamellae.


Animals ◽  
2021 ◽  
Vol 11 (2) ◽  
pp. 473
Author(s):  
Muhammad Rosyid Ridlo ◽  
Eui Hyun Kim ◽  
Anukul Taweechaipaisankul ◽  
Byeong Chun Lee ◽  
Geon A. Kim

The main factor of embryonic demise is endoplasmic reticulum (ER) stress. Successful attenuation of ER stress results in an improvement in embryo development. We studied the impact of adiponectin in the in vitro culture (IVC) of porcine embryos derived from parthenogenetic activation and somatic cell nuclear transfer (SCNT). The first experiment revealed that 15 and 30 μg/mL adiponectin treatments improved cleavage, blastocyst rates, and total cell number (TCN) of parthenogenetic embryos and reduced the expression of XBP1 compared to the 5 μg/mL adiponectin treatment and control groups (p < 0.05). The second experiment showed that cleavage rate, blastocyst formation rate, and TCN of blastocysts were improved in the 15 μg/mL adiponectin treatment group compared with the control group, with significantly reduced XBP1 expression in ≥4-cell stage SCNT embryos and blastocysts (p < 0.05). Treatment with 15 μg/mL adiponectin significantly improved the expression of XBP1 and reduced the expression of ER stress-related genes (uXBP1, sXBP1, PTPN1, and ATF4), increased the expression levels of pluripotency-related genes (Nanog and SOX2), and decreased apoptosis-related gene expression (Caspase-3). These results suggest that 15 μg/mL adiponectin enhanced the in vitro developmental capacity of early-stage SCNT porcine embryos by reducing ER stress and apoptosis.


Author(s):  
John J. Wolosewick ◽  
John H. D. Bryan

Early in spermiogenesis the manchette is rapidly assembled in a distal direction from the nuclear-ring-densities. The association of vesicles of smooth endoplasmic reticulum (SER) and the manchette microtubules (MTS) has been reported. In the mouse, osmophilic densities at the distal ends of the manchette are the organizing centers (MTOCS), and are associated with the SER. Rapid MT assembly and the lack of rough ER suggests that there is an existing pool of MT protein. Colcemid potentiates the reaction of vinblastine with tubulin and was used in this investigation to detect this protein.


Author(s):  
J. R. Ruby

Parotid glands were obtained from five adult (four male and one female) armadillos (Dasypus novemcinctus) which were perfusion-fixed. The glands were located in a position similar to that of most mammals. They extended interiorly to the anterior portion of the submandibular gland.In the light microscope, it was noted that the acini were relatively small and stained strongly positive with the periodic acid-Schiff (PAS) and alcian blue techniques, confirming the earlier results of Shackleford (1). Based on these qualities and other structural criteria, these cells have been classified as seromucous (2). The duct system was well developed. There were numerous intercalated ducts and intralobular striated ducts. The striated duct cells contained large amounts of PAS-positive substance.Thin sections revealed that the acinar cells were pyramidal in shape and contained a basally placed, slightly flattened nucleus (Fig. 1). The rough endoplasmic reticulum was also at the base of the cell.


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