Surface area ratios II. A stereological method for estimating changes in average cell volume and frequency

1979 ◽  
Vol 195 (2) ◽  
pp. 257-264 ◽  
Author(s):  
Robert P. Bolender
Keyword(s):  
Cell Volume ◽  
Surface Area ◽  
Average Cell ◽  
Stereological Method ◽  
Average Cell Volume

scholarly journals Cell tension and mechanical regulation of cell volume

2018 ◽  
Vol 29 (21) ◽  
pp. 0-0 ◽  
Author(s):  
Nicolas Perez Gonzalez ◽  
Jiaxiang Tao ◽  
Nash D. Rochman ◽  
Dhruv Vig ◽  
Evelyn Chiu ◽  
...  
Keyword(s):  
Cell Volume ◽  
Force Balance ◽  
Cell Cortex ◽  
Animal Cells ◽  
Mechanical Tension ◽  
Average Cell ◽  
Physical Size ◽  
Average Cell Volume ◽  
Cell Growth And Proliferation ◽  
Exclusion Method

Animal cells use an unknown mechanism to control their growth and physical size. Here, using the fluorescence exclusion method, we measure cell volume for adherent cells on substrates of varying stiffness. We discover that the cell volume has a complex dependence on substrate stiffness and is positively correlated with the size of the cell adhesion to the substrate. From a mechanical force–balance condition that determines the geometry of the cell surface, we find that the observed cell volume variation can be predicted quantitatively from the distribution of active myosin through the cell cortex. To connect cell mechanical tension with cell size homeostasis, we quantified the nuclear localization of YAP/TAZ, a transcription factor involved in cell growth and proliferation. We find that the level of nuclear YAP/TAZ is positively correlated with the average cell volume. Moreover, the level of nuclear YAP/TAZ is also connected to cell tension, as measured by the amount of phosphorylated myosin. Cells with greater apical tension tend to have higher levels of nuclear YAP/TAZ and a larger cell volume. These results point to a size-sensing mechanism based on mechanical tension: the cell tension increases as the cell grows, and increasing tension feeds back biochemically to growth and proliferation control.

Developmental stages of fetal-type Leydig cells in prepubertal rats

Development ◽  
1989 ◽  
Vol 107 (2) ◽  
pp. 213-220
Author(s):  
T. Kuopio ◽  
J. Tapanainen ◽  
L.J. Pelliniemi ◽  
I. Huhtaniemi
Keyword(s):  
Cell Volume ◽  
Leydig Cells ◽  
Developmental Stages ◽  
Neonatal Period ◽  
Microscopic Analysis ◽  
Electron Microscopic ◽  
Adult Type ◽  
Average Cell ◽  
Average Cell Volume ◽  
Fetal Leydig Cells

Fetal Leydig cells were studied in rats during and after the perinatal-neonatal period by comparing changes in morphology, number and volume with changes in testicular steroids and serum luteinizing hormone (LH) concentration. Stereologic examination indicated regression of fetal Leydig cells in testis by showing that their total volume as well as the average cell volume decreased between prenatal day 20 and postnatal day 3. The total number and total volume of cells both increased between postnatal days 3 and 11 but the average cell volume did not change during the same time period. Determination of serum LH showed a close correlation between an increase in LH concentration and increases in total number and volume of cells. The combined number of fetal- and adult-type Leydig cells on day 20 was more than 20 times the number of fetal cells at 3 days of age. Electron microscopic analysis showed that fetal Leydig cells after birth formed conspicuous clusters, which were surrounded by a layer of envelope cells and extracellular material. Occasional dividing fetal Leydig cells and possible precursors of fetal or adult Leydig cells were observed. Mitoses of spindle-shaped pericordal cells were frequent during the neonatal period. During and after the second postnatal week fetal Leydig cells again showed signs of regression, indicated by disintegration of the cell clusters, a decrease in cell size, accumulation of collagen between the cells and a decrease in steroid content per cell.(ABSTRACT TRUNCATED AT 250 WORDS)

scholarly journals Morphometric Assessment of Pulmonary Toxicity in the Rodent Lung

1991 ◽  
Vol 19 (4_part_1) ◽  
pp. 428-446 ◽  
Author(s):  
Dallas M. Hyde ◽  
David J. Magliano ◽  
Charles G. Plopper
Keyword(s):  
Cell Volume ◽  
Basal Lamina ◽  
Interstitial Cells ◽  
Nuclear Volume ◽  
Secretory Product ◽  
Average Cell ◽  
Interstitial Volume ◽  
Average Cell Volume ◽  
Morphometric Assessment ◽  
Cell Volumes

An overview of the epithelial and interstitial composition of rat respiratory airways shows complexity and variability. Airway epithelium varies in 1) different airway levels; 2) the types and ultrastructure of cells present; and 3) the abundance, type, and composition of stored secretory product. Unbiased sampling of airways is done using airway microdissection with a specific binary numbering system for airway generation. Vertical sections of selected airways are used to sample epithelium and interstitium. We determine the ratios of the volume of epithelial or interstitial cells to the total epithelial or interstitial volume (Vv). The surface of the epithelial basal lamina to the total epithelial or interstitial volume (Sv) is determined using point and intersection counting with a cycloid grid. Using the selector method on serial plastic sections, we determine the number of epithelial or interstitial cells per volume (Nv) of total epithelium or interstitium. We calculate the number of epithelial or interstitial cells per surface of epithelial basal lamina (Ns) by dividing Nv by Sv where the volumes are the same compartment. We calculate average cell volumes (v̄) for specific epithelial and interstitial cells by dividing the absolute nuclear volume by the ratio of the nucleus to cell volume (Vv). By multiplying the average cell volume (v̄) by the ratio of organellar volume to cell volume (Vv), we calculate the average organellar volume per cell. These unbiased stereological approaches are critical in a quantitative evaluation of toxicological injury of rat tracheobronchial airways.

scholarly journals BIOCHEMICAL AND MORPHOMETRIC PARAMETERS OF SOME ORGANS AND TISSUES OF HYBRID TILAPIA (OREOCHROMIS SPP.) FOR GROWING WITH USE OF PREPARATION ES-2

2018 ◽  
pp. 113-117
Author(s):  
Svetlana Vladimirovna Kotelnikova ◽  
Andrey Vyacheslavovich Kotelnikov ◽  
Alexander Nickolaevich Nevalennyy ◽  
Sergey Vladimirovich Ponomarev ◽  
Yulia Mikhailovna Shirina
Keyword(s):  
Lipid Peroxidation ◽  
Cell Volume ◽  
Control Group ◽  
Fish Feed ◽  
Prooxidant Effect ◽  
Average Cell ◽  
Liver Nuclei ◽  
Average Cell Volume ◽  
Experimental Group ◽  
Volume Decrease

The article studies the effect of addition into the feed of Sapropel extract (ES-2 preparation) on the intensity of lipid peroxidation in the liver and gills of hybrid tilapia ( Oreochromis spp. ), as well as on the morphofunctional state of its liver. Sapropel extract caused a decrease in the content of TBA-reactants in the tissues of tilapia liver by 17% compared to the control group. In gills the bioadditive resulted in the increased content of peroxide products by 24%. The introduction of ES-2 in fish feed resulted in reduction of spontaneous and ascorbate-dependent lipid peroxidation rate in the liver by 18%. In the gills of fish, under the influence of Sapropel, the rate of spontaneous lipid peroxidation increased by 27%, the rate of ascorbate-dependent lipid peroxidation - by 23%. The change in the intensity of peroxide processes under the influence of the fodder additive in fish organs is tissue-specific: antioxidant effect was recorded in the liver, prooxidant effect was observed in the gills. The introduction of the Sapropel extract does not lead to a change in the volume of liver nuclei in the test groups of tilapia, while the average cell volume in the experimental group was 37% lower than in the control group. The decrease in cell volume led to the increase in the nuclear-cytoplasmic ratio by 1.9 times in the experimental group compared to the control group. Hepatocyte cytoplasm volume decrease and nuclear-cytoplasmic ratio increase due to addition of ES-2 preparation into productive feed of hybrid tilapia would indicate a rise of functional activity of liver cells.

Desmosomes in hamster cheek pouch epithelium: their quantitative characterization during epithelial differentiation

1984 ◽  
Vol 66 (1) ◽  
pp. 411-429
Author(s):  
F.H. White ◽  
K. Gohari
Keyword(s):  
Plasma Membrane ◽  
Surface Area ◽  
Cheek Pouch ◽  
Unit Surface Area ◽  
Granular Cells ◽  
Hamster Cheek Pouch ◽  
Average Cell ◽  
Membrane Area ◽  
The Mean ◽  
Granular Layers

Desmosomes in stratified squamous epithelia appear to exhibit quantitative alterations during differentiation. In this work we use stereological and other morphometric methods to quantify these structures in epithelial cells from defined basal, spinous and granular strata. Hamster cheek pouch mucosa from five animals was processed for electron microscopy using strictly standardized techniques and a stratified random sampling procedure was used to obtain micrographs of cells from basal, spinous and granular layers. Stereological intersection counting techniques were used to determine for each layer the relative surface area of plasma membrane occupied by desmosomes (Ss), the number of desmosomes per unit surface area of plasma membrane (Ns), the mean individual desmosomal diameter (delta) and the mean individual desmosomal surface area (s). In addition, estimates of nuclear volume were obtained by direct measurement of nuclear profiles and volume-to-surface ratios were obtained by a combination of point and intersection counting, which enabled estimates for the volume (Vcell) and plasma membrane surface area (SPM) of the ‘average’ cell within each stratum to be acquired. Using this information, it was then possible to calculate both the total surface area (S) and the number (N) of desmosomes on the plasma membranes of average cells. The parameters Ss and Ns showed progressive increases between basal and granular layers, whereas values for delta and s were lower in granular cells when compared with basal and spinous cells. The parameters Vcell, SPM, S and N all increased progressively and significantly during differentiation. Between basal and granular layers, the mean cell volume and surface area had each increased approximately threefold, whereas the surface area and number of desmosomes on the average cell plasma membrane had increased approximately seven- and eleven-fold, respectively. Granular cells thus possess more numerous desmosomes, which occupy a greater proportion of the plasma membrane area but which are individually smaller, when compared with basal and spinous layers.

scholarly journals Red cell rheology in stomatocyte-echinocyte transformation: roles of cell geometry and cell shape

Blood ◽  
1986 ◽  
Vol 67 (4) ◽  
pp. 1110-1118 ◽  
Author(s):  
WH Reinhart ◽  
S Chien
Keyword(s):  
Cell Volume ◽  
Surface Area ◽  
Optimum Shape ◽  
Red Cell ◽  
Drug Induced ◽  
Filtration Resistance ◽  
Shear Rates ◽  
Geometric Factors ◽  
Shape Changes

Abstract The influence of the shape of the red blood cell during stomatocyte- echinocyte transformation on its deformability was studied by microsieving through pores with diameters of 2.6, 4.5, and 6.9 micron. A stomatocytic transformation was produced by chlorpromazine (0.02, 0.1, and 0.5 mmol/L) and an echinocytic transformation by sodium salicylate (7.5, 30, and 120 mmol/L). For spherostomatocytes, an increase in filtration resistance through 2.6 and 4.5 micron pores was observed, whereas for spheroechinocytes, a decrease in filtration resistance through 2.6 micron pores was found. Larger pores (6.9 micron) were not sensitive to those shape changes. The changes in deformability can be explained by the fact that the surface area of (sphero)-stomatocytes decreased, whereas that of (sphero)-echinocytes increased; the cell volume remained essentially constant. Echinocytes produced by 24-hour adenosine triphosphate depletion differed from drug- induced echinocytes: they had an increased cell volume at constant surface area and consequently an increased filtration resistance through 2.6- and 4.5-micron filter pores. Shape changes with spicule formation are therefore not a homogeneous entity, and cell geometric factors (eg, surface area and volume) must be assessed with care. The viscosity of red cell suspensions at a hematocrit level of 45% was higher for drug-induced echinocytes than discocytes or stomatocytes at all shear rates tested. We conclude that the normal discocyte represents an optimum shape for the flow in vivo since a stomatocytic transformation could impair the passage through the microcirculation (decrease in cell filterability) and an echinocytic transformation could impair the flow in larger vessels (increase in blood viscosity).

scholarly journals Differentiation of a teratocarcinoma line: preferential development of cholinergic neurons.

1981 ◽  
Vol 88 (1) ◽  
pp. 57-66 ◽  
Author(s):  
S E Pfeiffer ◽  
H Jakob ◽  
K Mikoshiba ◽  
P Dubois ◽  
J L Guenet ◽  
...  
Keyword(s):  
Morphological Changes ◽  
Cholinergic Neurons ◽  
Carcinoma Cells ◽  
Sodium Influx ◽  
Average Cell ◽  
Transmission Electron ◽  
Neuronal Processes ◽  
Embryonic Antigen ◽  
Average Cell Volume

A line of embryonal carcinoma cells, PCC7-S, established in vitro from a spontaneous testicular teratocarcinoma, has been studied. Upon removing the cells from a low density monolayer culture system and permitting the cells to form aggregates in suspension, we observed a change of several physical and biochemical parameters: (a) reduction in average cell volume, (b) blockage and accumulation of cells in G1, (c) rise in secreted protease activity, (d) rise in acetylcholinesterase and choline acetyltransferase activities, and (e) disappearance of embryonic antigen F9. Although PCC7 aggregates did not undergo substantial morphological changes while suspended, when aggregates 4 or more days old were allowed to attach to plastic tissue culture dishes, substantial neurite outgrowth occurred over the next 1-3 d. This process was markedly enhanced by the addition to the growth medium of carboxymethylcellulose and inhibitors of DNA synthesis. Transmission electron microscopy disclosed a neurite ultrastructure consistent with that of neuronal processes. A veratridine-stimulated, tetrodotoxin-blocked sodium influx of 100 nmol/min per mg protein was also observed in these differentiated surface cultures. This cell line is discussed in terms of its utility for the study of early events leading to a commitment to cellular differentiation, as well as for the investigation of terminal differentiation to cholinergic neurons.

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