Cell populations

In patients infected with HIV (human immunodeficiency virus), the helper cell population is weakened to the point where the immune system is no longer able to function properly. The body thus becomes susceptible to otherwise nonlethal diseases such as pneumonia. 

To include a linear decreasing function of the population size, the second-order cell population inhibition is considered ... 

The products that inhibit the cell population in the bioreactor and that promote the cell population gives ... 

Equation (3.14.2.26) is the novel population equation, which describes the cell population with inhibition or promotion.19,20... 

Figure 3.11 illustrates the mass transfer coefficient for batch-grown R. rubrum and was computed with various acetate concentrations at 200 rpm agitation speed, 500 lux light intensity, and 30 °C. As the experiment progressed, there was an increase in the rate of carbon monoxide uptake in the gas phase and a gradual decrease in die partial pressure of carbon monoxide. Also, a decrease in the partial pressure of carbon monoxide was affected by acetate concentration in the culture media. The value of the slope of the straight line increased with the decrease in acetate concentrations, i.e. 2.5 to 1 g-l. The maximum mass transfer coefficient was obtained for 1 g-l 1 acetate concentration (KLa = 4.3-h 1). The decrease in mass transfer coefficient was observed with the increase in acetate concentration. This was due to acetate inhibition on the microbial cell population as acetate concentration increased in the culture media. The minimum KLa was 1.2h 1 at 3g l 1 acetate concentration. 

Once there is an appreciable amount of cells and they are growing very rapidly, the cell number exponentially increases. The optical cell density of a culture can then be easily detected that phase is known as the exponential growth phase. The rate of cell synthesis sharply increases the linear increase is shown in the semi-log graph with a constant slope representing a constant rate of cell population. At this stage carbon sources are utilised and products are formed. Finally, rapid utilisation of substrate and accumulation of products may lead to stationary phase where the cell density remains constant. In this phase, cell may start to die as the cell growth rate balances the death rate. It is well known that the biocatalytic activities of the cell may gradually decrease as they age, and finally autolysis may take place. The dead cells and cell metabolites in the fermentation broth may create... 

The rate of product formation, rfi, depends upon the state of the cell population, environmental condition, temperature, pH, media composition and morphology with cell age distribution of the microorganism.2 3 A similar balance can be formulated for microbial biomass and cell concentration. The exponential phase of the microbial growth in a batch culture is defined by ... 

Biostat. This is also known as a turbidostat. It is a system where cell growth is controlled and remains constant while the flow rate of fresh media does not remain constant. Cell density is controlled based on set value for turbidity, which is created by the cell population while fresh media is continuously supplied. A turbidostat is shown in Figure 5.8. 

In fact, significant substrate concentration gradients may exist for cells immobilised in biofilm. Cells located close to the nutrient supply are likely to maintain higher quality and activity compared with cells located relatively further away, leading to differentiation in the quality or activity of the immobilised cell population. This differentiation is more pronounced if there are starvation regions. In practice, zero substrate concentration may exist inside the biofilm, because in these regions the cell physiology may be markedly different from that of the freely suspended cells. 

About 5 ml of sample is withdrawn for every 4-6 hours. The absorbance reading of the sample at 580 nm was measured using a Hitachi U-2000 spectrophotometer. The sample is filtered in a vacuum through Whatman filter paper with a pore size of 2.5 pin and diameter of 47 mm. The dry weight of cells is measured to monitoring microbial cell population and cell density. A plot of optical density reading from the spectrophotometer against cell dry... 

Cell-cycle arrest is the status of a cell population in which progression through the cell division cycle has been halted as a result of checkpoint activation. 

Differential display is a method for identifying differentially expressed genes, using anchored oligo-dT, random oligonucleotide primers and polymerase chain reaction on reverse-transcribed RNA from different cell populations. The amplified complementary DNAs are displayed and comparisons are drawn between the different cell populations. 

Hemangioblasts are the bipotential precursor cell population from which hematopoietic and angioblastic cells arise. 

This section gives models for the rates of birth, growth, and death of cell populations. We seek models for (1) the rate at which biomass is created, (2) the rates at which substrates are consumed, (3) the rates at which products are generated, (4) the maintenance requirements for a static population, and (5) the death rate of cells. The emphasis is on unstructured models. 

Maintenance requirements exist for nitrogen and other elements (e.g., phosphorous). They are relatively small, but must be supplied to maintain a stationary cell population. 

The lymphocytes from 31 patients exposed to various organophosphate pesticides were examined for chromosomal aberrations (Van Bao et al. 1974). Five of the patients were exposed to methyl parathion only. Blood samples were taken 3-6 days after exposure and again at 30 and 180 days. A significant (p<0.05) increase was noted in the frequency of stable chromosomal aberrations in acutely intoxicated persons (although such cells are eventually lost from the cell population). Two of the methyl parathion-exposed persons had taken large doses orally in suicide attempts. The study limitations include small sample size, absence of a control group, lack of quantification of exposure levels, and possible... 

Visual imaging of cell population in vitro) using low signal-to-noise ratio phase contrast microscopy can enable systematic monitoring measurements of cell quality, development and apoptosis. In the present study, microscopic evaluations as seen in Fig. 11 did not reveal any significant alteration in cellular morphology upto 1000 ng/ml. 

A method of assessing the toxicity of implants has been proposed based on the effects on cell ultrastructure in organ cultures, on cell surface characteristics, and cell population doubling times. The effects have been correlated with hemorrhage, fibrosis, and necrosis, respectively (103). Poly-e-caprolactone was stated to give minimal tissue reaction and could not be scored in these tests. 

Wollenberg A. Kraft S. Hanau D. Bieber T Immuno-morphological and ultrastructural characterization of Langerhans cells and a novel, inflammatory dendritic epidermal cell population in lesional skin of atopic eczema. J Invest Dermatol 1996 106 446-453. 

The in vivo relevance and biological importance of in vitro observations about mast cell function, as well as the contributions of mast cells towards the expression of particular biological responses (such as various models of anaphylaxis) in vivo, can be assessed using c-kit mutant mice (e.g., WBB6Fi-FCit or mice) that virtually lack mast cell populations. Mice with mutations of c-kit [6,11] or mutations that affect KIT expression [12-14] have other abnormalities of phenotype besides a mast cell deficiency. However, the mast cell deficiency of these mice can be selectively repaired by the adoptive transfer of genetically compatible, in vitro-derived... 

Brittain E, Noel P, Metcalfe DD Demonstration of an aberrant mast-cell population with clonal markers in a subset of patients with idiopathic anaphy- 72 laxis. Blood 2007 110 2331-2333. 

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