Effect Of Growth Factors Fcs On Cell Proliferation Biology Essay

Effect Of Growth Factors Fcs On Cell Proliferation Biology Essay initiationThe technique in which stalls normally of one type, removed from animal tissue ar grown in presence of supplements and growth factors under controlled conditions is called Cell Culturing. diverse cellphones require different conditions of temperature and gas for their appropriate growth in a cell incubator moreover growth media plays a crucial role in cell culturing, which can vary in glucose concentration, pH, growth factors like fetal calf serum (FCS).The effect of one of the above mentioned variables, we are going to adopt in this experiment is growth factors. Growth factors as the name suggests enhancers the growth which supplements the media are obtained from animal blood such as calf serum.Cell proliferation is examine by various methods, mainly used methods involve measuring the colour persuasiveness taken up by desoxyribonucleic acid of cell during cell proliferation in presence of staining dy es e.g. quartz royal and MTT (3-(4,5-dimethyl thiazol-2-yl)-2,5-diphenyl tetrazolium bromide).The aim of this experiment is to study cell proliferation by using crystallisation violet and MTT methods while using pilfer Y1 adrenocortical cells under the effect of growth factor FCS. pinch Y1 adrenocortical cell are grown in Dulbeccos modification of Eagles mass medium as monolayer cultures.watch glass VioletIt is biological stain used in cell proliferation method which stains DNA of the cells after permeabilisation with methanol. The positive ammonium ions of crystal violet stain DNA of cells in blue colour.The colour intensity produced is directly proportional to number of cells, which is determined in stain cells by colorimeter. Staining with crystal violet and MTT are based on principal of absorbance.MTTThe MTT assay is a standard colorimetric assay in which activity of reductase enzymes are measured which convert MTT to blue indissoluble formazan. The metabolic activity of viable cells is used as basic parameter in MTT assay. The tetrazolium salt, MTT is now widely used in quantitative measurement of cell proliferation. This method depends upon uptake of MTT by viable cells, which is a water supply soluble tetrazolium salt producing a yellowish solution. MTT is cleaved to insoluble blue formazan in the mitochondria of living cells by succinic dehydrogenases in the mitochondrial respiratory chain.Material UsedMouse Y1 adrenocortical cells, Dulbeccos medication of Eagles medium (DMEM) containing 10% Fetal calf serum, 2mM glutamine, 100u/ml penicillin and 100mg/ml streptomycin, crystal violet stain (0.1% solution in 200mM boric acid), MTT (5mg/ml MTT solution in PBS), PBS methanol, 10% glacial acetic acid, distilled water, acid-isopropanol.Apparatus used stratified flow cabinet sterilized two 96 well plates, multi well pipettes, pasture pipettes, sterilized T-flasks, sterilised empty reservoirs, gas incubator, fume water closet, spectrophotometer etc. m annerCells of mouse Y1 adrenocortical were separated from their substratum with tris in EDTA as they grow in monolayer cultures. Then added same volume of medium and centrifuged after that number of cells were counted on haemocytometer and diluted to concentration of 1.25 105 cells/ml and made it up to 30 ml.Then cells were passaged into centre 60 wells of 96 well plate in duplicate with concentration of 0.25 10 cells/ 200l in each well while outside wells of 96 well plate were fill with same amount of phosphate buffered saline (PBS) and allowed the cells to incubate overnight at 37 C temperature in humidified gas incubator. by and by that cells were washed with PBS tercet times and different wells of each plate were do by with different concentrations of FCS which is shown in table 1.Hence 12 wells of each plate were treated with 0, 1, 5, 10 and 20% v/v concentration of FCS and both plates were incubated for 72 hours.One plate was used for crystal violet staining method and s ome other for MTT assay.Table 1Dilution of FCS% FCSVolume of Serum(ml)Volume of Medium (ml)001010.19.950.59.510192028 crystal violet staining methodFor this method cell media was removed first of all from incubated plate and then cells were washed with PBS. later that were fixed with 200l of methanol for 15 minutes in fume cupboard. Then methanol were removed and cells were allowed to dry in fume cupboard for few minutes.Then cells were treated for 20 minutes with crystal violet stain 200l/well. Later cells were washed three times with distilled water and stained cell layer was allowed to solubilised in the 50l of 10% glacial acetic acid and plates were incubated for 30 minutes in gas incubator.After that absorbance of each well was read by plate reviewer spectrophotometer set at 540nm.MTT MethodTo perform MTT assay, each of centre 60 wells of 96 well plate was treated with 20l of MTT solution and plate was incubated for 4 hours at 37o C temperature in gas incubator.After 4 hours, the medium was removed from each well and 100l of acid-isopropand was added to dissolve blue formazan crystal in the cell layer. Then plate was incubated for 30 minutes at room temperature.When blue formazan crystal were solubilised, absorbance of each well was measured at 570nm using the plate reader.CalculationsCells in five consecutives of Haemocytometer = 24Volume of each square is =4-10-3lThe no. of cells in five squares multiplied with 5-104 gives no. of cells in 1ml.Hence no. of cell in 1ml = 1.2-106 cells/ml call for cell breach = 1.25-105 cells/mlDilution Factor = Concentration Required/Concentration gotDilution Factor = 0.104Therefore, in order to make 30 ml of cell suspension 3.125 ml of cell suspension was mixed with 26.875 ml of medium.Similarly 30 ml of cell suspension was prepared having 1.25-105 cells/ml.ResultsObservation Table for crystal violet staining method%FCSAverageStandard Deviation00.2050.021810.2550.030750.3090.0450100.4320.0614200.5810.0844Table2 Data o btain from plate reader at 540nmGraph showing effect of FCS with Crystal Violet MethodAbove graph shows that with increase in serum concentration the absorbance increases, which is directly proportional to cell number.Observation Table of MTT staining method% FCSAverageStandard Deviation00.0940.008110.1150.013850.1520.0191100.2760.0724200.4000.0807Table3 Data obtained from plate reader at 570nm.Graph showing effect of FCS with MTT stainingAbove graph shows that with increase in serum concentration the absorbance increases, which is directly proportional to cell number. intelligenceCrystal Violet Staining method and MTT Assay is based on principle of absorbance, more is colour intensity, more will be the absorbance value.The result of Crystal violet staining method clearly indicated that absorbance value was directly proportional to cell proliferation as it was increasing with concentration of FCS.FCS stimulated Cell ProliferationResult in more cells and DNAMethanol increased cell me mbrane permeabilityResult in more stained DNAMore Colour intensityHence More Absorbance ValueSimilar results were seen in MTT Assay but in this assay only viable cells were stained while in crystal violet method both viable and non viable cells were stained. So Crystal Violet method of staining is not specific staining technique because in this absorbance is not direct index of cell viability.The drawback of MTT Assay is that some reducing agent may reduce MTT also which could show slight increase in absorbance, moreover this method depends on some variable like pH, presence of D-glucose and pyridine nucleotides which can affect the specificity of Assay.In spite of above said limitations these methods are broadly followed because they are safe, simple, cheap and reproducible. eminence of K562 cells to megakaryocytes/plateletsTo study cell differentiation of K652 cells chronic myelogenous leukaemia, K652 cell line, indicates an early differentiation stage of granulocyte lineage. K65 2 cells are non-adherent, circular shaped with petite microvilli.In the presence of tumour promoters like phorbol myristate acetate (PMA) these type of cell are differentiated to megakaryocytes.The induction of megakaryocytic differentiation of K652 cells is known to be initiated by two signalling pathways which are the nuclear factor kappa B(NF-B) -depends pathways and other is extracellular signal regulated kinase (ERK)/mitogen activated kinase (MAPK) dependent pathways.Human chromic myelogenous leukemic cells, K652 cells have Philadelphia chromosome. Tumour promoter, PMA which is a pissed mitogen for human peripheral blood lymphocyte also act as a protein kinase C (PKC) activator which differentiate K652 cells to megakaryocytes.The various changes that occurs during differentiation of K652 cells areChanges in cell morphologyCell growth arrestAdhesive properties of cell changeExpression of markers associatated with megakaryocytesEndomitosisNADPH oxidase complex which is know n as a primary source of ROS (Radio prompt oxygen species), is initiated by PMA.PMA stimulates NADPH ROS (Signalling Molecule)Induction of gene reflectivity is directly related with ROS.The Expression of CD61, a platelet cell marker helps in identifying differentiated cells. The expression of CD61 can be seen on platelets, osteoclasts, macrophages and on some tumour cells, involved in tumour metastasis and in adenovirus infections.Results and DiscussionIt was observed that PMA treated slide was stained pink while cells devoid of PMA were stained blue as shown in Pic. 1 2. In PMA treated slide the K562 cells were clearly differentiated to megakaryocytes which suggested that tumour promoter, PMA bring on differentiation in K562 cells by signal transduction and expressed by CD61 as shown in picture below.CUsersmkkaushalPicturescell bio picsmail2.jpg Pic. 1PMA Treated Cells clearly showing Differentiation to MegakaryocytesCUsersmkkaushalPicturescell bio picsmail.jpg Pic. 2Cells Devoi d of PMA stained blue in ColourThe expression of CD61 was recognised by addition of rabbit anti-mouse IgG antibodies that bind to CD61 antibodies when incubated in presence of alkaline phosphatise anti alkaline phosphatise (APAAP) complex.The cells were stained pink because fast red dye get attached to APAAP so this is how CD61 was expressed in cell treated with PMA. Moreover cells treated with PMA were larger, irregular, in shape and fewer in number as compare to untreated cells.On the contrary, Cells devoid of PMA were much smaller in size than treated cells.Diagramatic Representations of ImmunocytochemicalReactions To Detect CD61PMA Treated Cells PMA Untreated CellsCD61 bound to both treated and untreated cellsThen Cells are washed toRemove CD61 unbound Treated with RAMThen RAM binds to APAAP and cells are stained pink in colour. Mouse Antihuman CD 61 (PrimaryAntibody) Rabbit Antimouse IgG (RAM-Secondary Antibody) Mouse Alkaline Phosphate AntiAlkalinePhosphatase(APAAP Tertiary Antibody)