Nuclear size as a cell-kinetic marker for osteoblast differentiation

1982 ◽  
Vol 165 (4) ◽  
pp. 373-384 ◽  
Author(s):  
W. Eugene Roberts ◽  
Peter G. Mozsary ◽  
Eliane Klingler
1993 ◽  
Vol 63 (4) ◽  
pp. 509-517 ◽  
Author(s):  
G.M. Morris ◽  
W. Landuyt ◽  
E. Whitehouse ◽  
L. Vanuytsel ◽  
J.W. Hopewell

Transfusion ◽  
2000 ◽  
Vol 40 (11) ◽  
pp. 1363-1370 ◽  
Author(s):  
Andreas Humpe ◽  
Joachim Riggert ◽  
Ingolf Meineke ◽  
Martin Kurz ◽  
Anita Eil ◽  
...  

Cancer ◽  
1985 ◽  
Vol 55 (8) ◽  
pp. 1711-1713 ◽  
Author(s):  
Takao Hoshino ◽  
Shu Kobayashi ◽  
Jeannette J. Townsend ◽  
Charles B. Wilson
Keyword(s):  

2013 ◽  
Vol 24 (15) ◽  
pp. 2442-2453 ◽  
Author(s):  
Yuki Hara ◽  
Mari Iwabuchi ◽  
Keita Ohsumi ◽  
Akatsuki Kimura

Chromosome condensation is critical for accurate inheritance of genetic information. The degree of condensation, which is reflected in the size of the condensed chromosomes during mitosis, is not constant. It is differentially regulated in embryonic and somatic cells. In addition to the developmentally programmed regulation of chromosome condensation, there may be adaptive regulation based on spatial parameters such as genomic length or cell size. We propose that chromosome condensation is affected by a spatial parameter called the chromosome amount per nuclear space, or “intranuclear DNA density.” Using Caenorhabditis elegans embryos, we show that condensed chromosome sizes vary during early embryogenesis. Of importance, changing DNA content to haploid or polyploid changes the condensed chromosome size, even at the same developmental stage. Condensed chromosome size correlates with interphase nuclear size. Finally, a reduction in nuclear size in a cell-free system from Xenopus laevis eggs resulted in reduced condensed chromosome sizes. These data support the hypothesis that intranuclear DNA density regulates chromosome condensation. This suggests an adaptive mode of chromosome condensation regulation in metazoans.


Neurosurgery ◽  
1986 ◽  
Vol 19 (6) ◽  
pp. 900-904 ◽  
Author(s):  
Judith A. Murovic ◽  
Tadashi Nagashima ◽  
Takao Hoshino ◽  
Michael S. B. Edwards ◽  
Richard L. Davis

Abstract Bromodeoxyuridine (BrdU), 150 to 200 mg/m2, was administered at the time of operation to 20 pediatric patients with neuroectodermal tumors to label tumor cells in the S phase. Immunocytochemical techniques were used on excised tumor specimens to detect cells containing BrdU, and the BrdU labeling index (LI) was calculated as the number of BrdU-labeled cells divided by the total number of cells counted. Four medulloblastomas, three glioblastomas multiforme, and two highly anaplastic astrocytomas had average BrdU LIs of 13.0 ± 3.0% (SE), 12.7 ± 4.3%, and 14.6 ± 6.7%, respectively. Three of nine moderately anaplastic astrocytomas had BrdU LIs of greater than 1% (average, 6.5 ± 2.4%), whereas six had LIs of less than 1%. In two juvenile pilocytic astrocytomas, which are considered slow-growing, the BrdU LIs were unexpectedly high, averaging 6.5 ± 1.4%. Thus, pediatric medulloblastomas, glioblastomas multiforme, highly anaplastic astrocytomas, and a minority of moderately anaplastic astrocytomas had high proliferative potentials, whereas most of the moderately anaplastic astrocytomas had low proliferative potentials. Although the number of cases in this study is still too small to yield statistically significant comparisons, the results indicate that some pediatric tumors have considerably higher LIs than histologically similar adult tumors studied previously.


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