Recently, the biological and biochemical characteristics of EMC virus have received considerable attention, but little is known concerning the relative susceptibility of various mammalian cells to EMC virus. In this study, a variety of mammalian cell types was evaluated for susceptibility to the M s
Number of nucleoli in various cell types of the mouse
โ Scribed by J. R. Shea Jr.; C. P. Leblond
- Publisher
- John Wiley and Sons
- Year
- 1966
- Tongue
- English
- Weight
- 731 KB
- Volume
- 119
- Category
- Article
- ISSN
- 0362-2525
No coin nor oath required. For personal study only.
โฆ Synopsis
The nucleoli of cells of the adult mouse were examined by staining with toluidine blue after removal of deoxyribonucleic acid from tissue sections by deoxyribonuclease treatment.
The nuclei of each cell type examined contained one or more nucleoli. This was observed even in lymphocytes and neuroglia, although these cells have occasionally been described as anucleolated. In mature spermatids and spermatozoa, however, it was not possible to detect a nucleolus.
The distribution of the number of nucleoli in many diploid cells exhibited a m o d e of two or three nucleoli per nucleus, and a range from 1 to 6 nucleoli.
In presumedly diploid hepatic nuclei, the maximum number of nucleoli was six; but in presumedly tetraploid hepatic nuclei, it was 11. Thus, nearly twice as many nucleoli are present when the chromosome number is doubled. In view of this observation, it is suggested that six nucleolar organizers are present in the diploid chromosomal complement of the mouse. However, through failure of some nucleolar organizers or more probably through fusion of nucleoli, the number of these organelles in most nuclei is less than six.
๐ SIMILAR VOLUMES
## Abstract The presence of fibrin deposits in the micro environment of tumor cells has been reported repeatedly and considered to play an important role in tumor biology. Among the mechanisms by which fibrin may be deposited in tumors, procoagulant activities (PCA) of different types have been des
Low viability of manipulated or in vitro cultured embryos is caused primarily by the reduced cell number in the implanting blastocysts. In order to investigate the effect of implantation delay on embryo viability and cell number, mouse blastocysts were transferred into oviducts of day 0 pseudopregna