Age and sex do not affect the volume, cell numbers, or cell size of the suprachiasmatic nucleus of the rat: An unbiased stereological study

1995 ◽  
Vol 361 (4) ◽  
pp. 585-601 ◽  
Author(s):  
M. Dulce Madeira ◽  
N. Sousa ◽  
R. M. Santer ◽  
M. M. Paula-Barbosa ◽  
H. J. G. Gundersen
Endocrinology ◽  
2006 ◽  
Vol 147 (4) ◽  
pp. 1904-1915 ◽  
Author(s):  
S. McArthur ◽  
Z.-L. Siddique ◽  
H. C. Christian ◽  
G. Capone ◽  
E. Theogaraj ◽  
...  

This study aimed to test the hypothesis that the tuberoinfundibular dopaminergic neurons of the arcuate nucleus and/or the lactotroph cells of the anterior pituitary gland are key targets for the programming effects of perinatal glucocorticoids (GCs). Dexamethasone was administered noninvasively to fetal or neonatal rats via the mothers’ drinking water (1 μg/ml) on embryonic d 16–19 or neonatal d 1–7, and control animals received normal drinking water. At 68 d of age, the numbers of tyrosine hydroxylase-positive (TH+) cells in the arcuate nucleus and morphometric parameters of pituitary lactotrophs were analyzed. In control animals, striking sex differences in TH+ cell numbers, lactotroph cell size, and pituitary prolactin content were observed. Both pre- and neonatal GC treatment regimens were without effect in adult male rats, but in females, the overriding effect was to abolish the sex differences by reducing arcuate TH+ cell numbers (pre- and neonatal treatments) and reducing lactotroph cell size and pituitary prolactin content (prenatal treatment only) without changing lactotroph cell numbers. Changes in circulating prolactin levels represented a net effect of hypothalamic and pituitary alterations that exhibited independent critical windows of susceptibility to perinatal GC treatments. The dopaminergic neurons of the hypothalamic periventricular nucleus and the pituitary somatotroph populations were not significantly affected by either treatment regimen in either sex. These data show that the adult female hypothalamo-lactotroph axis is profoundly affected by perinatal exposure to GCs, which disrupts the tonic inhibitory tuberoinfundibular dopaminergic pathway and changes lactotroph morphology and prolactin levels in the pituitary and circulation. These findings provide new evidence for a long-term disruption in prolactin-dependent homeostasis in females, but not males, after inappropriate GC exposure in perinatal life.


1986 ◽  
Vol 64 (9) ◽  
pp. 2165-2167
Author(s):  
K. I. Thomas ◽  
R. E. Wall

The stem tissues of yellow birch (Betula alleghaniensis Britton) saplings, with wavy bands of stained xylem parallel to the annual rings and depressions in the xylem at the xylem–phloem interface (stem pitting), were studied microscopically. The bands of stained xylem consisted of abnormally formed parenchyma (parenchymatous wood) interspersed with collapsed cells. Rays in the affected areas showed increases in both cell numbers and cell size, often being indistinguishable from adjacent parenchymatous wood. Aggregate rays were associated with stained bands as well as with stem pitting in the xylem and corresponding protrusions of the phloem.


2021 ◽  
Vol 11 (1) ◽  
Author(s):  
Ravangnam Thunyaporn ◽  
Il Doh ◽  
Dong Woo Lee

AbstractCell counting has become an essential method for monitoring the viability and proliferation of cells. A hemacytometer is the standard device used to measure cell numbers in most laboratories which are typically automated to increase throughput. The principle of both manual and automated hemacytometers is to calculate cell numbers with a fixed volume within a set measurement range (105 ~ 106 cells/ml). If the cell concentration of the unknown sample is outside the range of the hemacytometer, the sample must be prepared again by increasing or decreasing the cell concentration. We have developed a new hemacytometer that has a multi-volume chamber with 4 different depths containing different volumes (0.1, 0.2, 0.4, 0.8 µl respectively). A multi-volume hemacytometer can measure cell concentration with a maximum of 106 cells/ml to a minimum of 5 × 103 cells/ml. Compared to a typical hemacytometer with a fixed volume of 0.1 µl, the minimum measurable cell concentration of 5 × 103 cells/ml on the multi-volume hemacytometer is twenty times lower. Additionally, the Multi-Volume Cell Counting model (cell concentration calculation with the slope value of cell number in multi-chambers) showed a wide measurement range (5 × 103 ~ 1 × 106 cells/ml) while reducing total cell counting numbers by 62.5% compared to a large volume (0.8 µl-chamber) hemacytometer.


Development ◽  
1965 ◽  
Vol 14 (1) ◽  
pp. 15-24
Author(s):  
A. W. Marrable

This paper reports a study of the timing of early cleavage divisions in the zebra fish and of the changes that occur during cleavage in cell size and number. The eggs of the zebra fish Brachydanio rerio (Hamilton-Buchanan) were used in these studies. Roosen-Runge (1936, 1938, 1939), Marrable (1959, 1962a) and others have described various aspects of the biology of this fish when maintained in the laboratory. It is a freshwater tropical teleost, the females laying nonsticky, non-pigmented demersal eggs which undergo a regular and predictable pattern of cleavage; fertilization is external and the diameter of the spheroidal chorion enclosing each egg is about 800 μ. Breeding is normally promiscuous but when monogamy is imposed hundreds of fertile eggs can be obtained. Development is rapid: at 27·25±0·5°C. the first cleavage is 30 min. after fertilization; there are 32 cells after 90 min. and gastrulation takes place after about 4 hr.


2021 ◽  
Author(s):  
Thunyaporn Ravangnam ◽  
Il Doh ◽  
Dong Woo Lee

Abstract Cell counting has become an essential method for monitoring the viability and proliferation of cells. A hemacytometer is the standard device used to measure cell numbers in most laboratories which are typically automated to increase throughput. The principle of both manual and automated hemacytometers is to calculate cell numbers with a fixed volume within a set measurement range (105~106 cells/ml). If the cell concentration of the unknown sample is outside the range of the hemacytometer, the sample must be prepared again by increasing or decreasing the cell concentration. We have developed a new hemacytometer that has a multi-volume chamber with 4 different depths containing different volumes (0.1, 0.2, 0.4, 0.8 µl respectively). A multi-volume hemacytometer can measure cell concentration with a maximum of 106 cells/ml to a minimum of 5×103 cells/ml. Compared to a typical hemacytometer with a fixed volume of 0.1 µl, the minimum measurable cell concentration of 5×103 cells/ml on the multi-volume hemacytometer is twenty times lower. Additionally, the Multi-Volume Cell Counting model (cell concentration calculation with the slope value of cell number in multi-chambers) showed a wide measurement range (5×103 ~1×106 cells/ml) while reducing total cell counting numbers by 62.5% compared to a large volume (0.8 µl-chamber) hemacytometer.


HortScience ◽  
2005 ◽  
Vol 40 (4) ◽  
pp. 1008B-1008 ◽  
Author(s):  
James W. Olmstead ◽  
Amy F. Iezzoni ◽  
Matthew D. Whiting

Although maximizing fruit size is critical for profitable sweet cherry (Prunusavium L.) production, little is known about the cellular differences among and between cultivars that contribute to fruit size differences. A wide range of fruit size exists among sweet cherries, and, due to cultural and environmental differences, significant variation exists among genetically identical fruit from the same cultivar. To determine the relative contributions of flesh cell number and cell size to final fruit size in sweet cherry, equatorial sections of three cultivars with a wide range in final average fruit size [`New York 54' (NY54; 1.4 g fresh weight, 11.8 mm diameter), `Emperor Francis' (EF; 6.1 g, 21.0 mm), and `Selah' (12.8 g, 25.5 mm)] were created from mature fruit. Cells intersecting a transverse line were counted and average cell length was calculated. The average cell numbers were significantly different (P ≤ 0.05) between `NY54', `EF', and `Selah' (26.7, 47.4, and 83.2, respectively), indicating that flesh cell number is the major contributor to differences in fruit size between cultivars. Flesh cell numbers of `NY54', `EF', and `Selah' were similar at bloom and increased rapidly for a short duration after fertilization, suggesting a key developmental period for fruit size differences. To determine the contribution of cell number differences to variation in fruit size within a cultivar, fruit from `Bing' and `Regina' trees exhibiting a range of size due to cultural and environmental differences were measured. In both cases, average cell number was not significantly different (P = 0.9, P = 0.3, respectively), while average cell size was (P ≤ 0.05), further indicating fruit flesh cell number is a genetically controlled trait.


2015 ◽  
Vol 221 (7) ◽  
pp. 3547-3559 ◽  
Author(s):  
Ana V. Oliveira-Pinto ◽  
Carlos H. Andrade-Moraes ◽  
Lays M. Oliveira ◽  
Danielle R. Parente-Bruno ◽  
Raquel M. Santos ◽  
...  

Reproduction ◽  
2004 ◽  
Vol 127 (6) ◽  
pp. 669-677 ◽  
Author(s):  
G Wycherley ◽  
D Downey ◽  
M T Kane ◽  
A C Hynes

This study reports a novel, simple method for culture of mouse follicles which results in follicles with cell numbers similar toin vivofully grown follicles. Using this method, follicles (180–240 μm in diameter) were cultured in a 100 μl inverted drop of medium without oil and compared with culture in upright drops with and without a mineral oil overlay. Follicles, isolated from C57BL/6 × CBA/ca crossbred and MF1 inbred mice, were cultured individually at 37 °C in 96-well round-bottomed suspension cell tissue culture plates for 6 days. Follicles grown in the inverted drop culture system reached a markedly higher final diameter (means±s.e.m.; 471 ± 6.0 μm) as compared with the upright with oil (363 ± 2.7 μm) and without oil (358 ± 4.0) systems. There was no significant effect of mouse strain on follicle diameter. Follicular secretion of oestradiol and lactate into the medium was measured on days 2, 4 and 6 of culture. Secretion of oestradiol per follicle on day 6 was 2.49 ± 0.45 ng in the inverted and 0.90 ± 0.17 ng in the upright without oil system (P< 0.001). Follicular secretion of lactate on a per unit of follicle volume basis remained constant in the inverted system over days 2, 4 and 6 and was less (P< 0.001) than secretion in both the upright with and without oil systems. Follicle cell proliferation was markedly increased in the inverted as compared with the upright with oil system; the increases in cell numbers were significant on day 3 (P< 0.01) and on all subsequent days (P< 0.001). These results are discussed in relation to the supply of oxygen to the follicle in culture.


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