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Lec Mammalian Cell Culture.ppt

Cell culture is the process of growing cells under controlled conditions outside of their natural environment. Some key developments in cell culture technology include the use of antibiotics to prevent contamination, trypsin to detach adherent cells for subculture, and chemically defined culture media. Cell culture has many applications, including modeling basic cell biology, cancer research, genetic engineering, gene therapy, and vaccine production. Proper equipment, aseptic technique, and safety precautions are required to successfully culture cells.

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Basics of Cell Culture Lecture Dr. Maryam Zafar
Introduction  Cell culture is the process by which prokaryotic, eukaryotic or plant cells are grown under controlled conditions. But in practice it refers to the culturing of cells derived from animal cells.  Cell culture was first successfully undertaken by Ross Harrison in 1907  Roux in 1885 for the first time maintained embryonic chick cells in a cell culture
Major development’s in cell culture technology  First development was the use of antibiotics which inhibits the growth of contaminants.  Second was the use of trypsin to remove adherent cells to subculture further from the culture vessel  Third was the use of chemically defined culture medium.
Applications of cell culture Areas where cell culture technology is currently playing a major role.  Model systems for Studying basic cell biology, interactions between disease causing agents and cells, effects of drugs on cells, process and triggering of aging & nutritional studies  Toxicity testing Study the effects of new drugs  Cancer research Study the function of various chemicals, virus & radiation to convert normal cultured cells to cancerous cells
Contd….  Virology Cultivation of virus for vaccine production, also used to study there infectious cycle.  Genetic Engineering Production of commercial proteins, large scale production of viruses for use in vaccine production e.g. polio, rabies, chicken pox, hepatitis B & measles  Gene therapy Cells having a functional gene can be replaced to cells which are having non-functional gene
What is Tissue culture?  In vitro cultivation of organs, tissues & cells at defined temperature using an incubator & supplemented with a medium containing cell nutrients & growth factors is collectively known as tissue culture  Different types of cell grown in culture includes connective tissue elements such as fibroblasts, skeletal tissue, cardiac, epithelial tissue (liver, breast, skin, kidney) and many different types of tumor cells.
Primary culture  Cells when surgically or enzymatically removed from an organism and placed in suitable culture environment will attach and grow are called as primary culture  Primary cells have a finite life span  Primary culture contains a very heterogeneous population of cells  Sub culturing of primary cells leads to the generation of cell lines  Cell lines have limited life span, they passage several times before they become senescent  Lineage of cells originating from the primary culture is called a cell strain
Difference in Finite and Continuous cell lines?  Finite cell lines - The cell lines which have a limited life span and go through a limited number of cell generations (usually 20-80 population doublings) are known as finite cell lines. These cell lines exhibit the property of contact inhibition, density limitation and anchorage dependence. The growth rate is slow and doubling time is around 24-96 hours.  Continuous cell lines Most cell lines grow for a limited number of generations after which they ceases. Cell lines which either occur spontaneously or induced virally or chemically transformed into Continuous cell lines
Types of cells On the basis of morphology (shape & appearance) or on their functional characteristics. They are divided into three.  Epithelial like-attached to a substrate and appears flattened and polygonal in shape  Lymphoblast like- cells do not attach remain in suspension with a spherical shape  Fibroblast like- cells attached to an substrate appears elongated and bipolar
Culture media  Choice of media depends on the type of cell being cultured  Commonly used Medium are EMEM, DMEM etc.  Media is supplemented with antibiotics viz. penicillin, streptomycin etc.  Prepared media is filtered and incubated at 4 C
Why sub culturing.?  Once the available substrate surface is covered by cells (a confluent culture) growth slows & ceases.  Cells to be kept in healthy & in growing state have to be sub-cultured or passaged  It’s the passage of cells when they reach to 80- 90% confluency in flask/dishes/plates  Enzyme such as trypsin, dipase, collagenase breaks the cellular glue that attached the cells to the surface
Culturing of cells  Cell lines derived from normal tissues are considered as anchorage-dependent grows only on a suitable substrate e.g. tissue cells  Suspension cells are anchorage-independent e.g. blood cells  Transformed cell lines either grows as monolayer or as suspension
Adherent cells  Cells which are anchorage dependent  Cells are washed with PBS solution.  Incubate the plate at 37 C for 1-2 mins  Tap the vessel from the sides to dislodge the cells  Add complete medium to dissociate and dislodge the cells  with the help of pipette which are remained to be adherent  Add complete medium depends on the subculture  requirement either to 75 cm or 175 cm flask
Suspension cells  Easier to passage as no need to detach them  As the suspension cells reach to confluency  Aseptically remove 1/3rd of medium  Replaced with the same amount of pre-warmed medium
Freezing cells for storage  Remove the growth medium, wash the cells by PBS and remove the PBS by aspiration  Dislodge the cells by trypsin-versene  Dilute the cells with growth medium  Transfer the cell suspension to a 15 ml conical tube, centrifuge at 200g for 5 mins at room temp and remove the growth medium by aspiration  Resuspend the cells in 1-2 ml of freezing medium  Transfer the cells to cryovials, incubate the cryovials at -80 C overnight  Next day transfer the cryovials to Liquid nitrogen
Cell viability  Cell viability is determined by staining the cells with trypan blue  As trypan blue dye is permeable to non-viable cells or death cells whereas it is impermeable to this dye  Stain the cells with trypan dye and load to hemocytometer and calculate % of viable cells % of viable cells= Number of unstained cells x 100 total number of cells
Common cell lines  MCF-7 breast cancer  HL 60 Leukemia  HEK-293 Human embryonic kidney  HeLa Henrietta lacks  Vero African green monkey kidney epithelial cells  Cos-7 African green monkey kidney cells  And others such as CHO from Chinese hamster ovary cells, sf9 & sf21 from insect cells
Basic equipment's used in cell culture  Biological safety cabinet-Vertical are preferable  Incubation facilities- Temperature of 25-30 C for insect & 37 C for mammalian cells, co2 2-5% & 95% air at 99% relative humidity. To prevent cell death incubators set to cut out at approx. 38.5 C  Refrigerators- Liquid media kept at 4 C, enzymes (e.g. trypsin) & media components (e.g. glutamine & serum) at - 20 C  Microscope- An inverted microscope with 10x to 100x magnification  Tissue culture ware- Culture plastic ware treated by polystyrene
Basic aseptic conditions  If working on the bench use a Bunsen flame to heat the air surrounding the Bunsen  Swab all bottle tops & necks with 70% ethanol  Flame all bottle necks & pipette by passing very quickly through the hottest part of the flame  Avoiding placing caps & pipettes down on the bench; practice holding bottle tops with the little finger  Work either left to right or vice versa, so that all material goes to one side, once finished  Clean up spills immediately & always leave the work place neat & tidy
Safety aspect in cell culture  Possibly keep cultures free of antibiotics in order to be able to recognize the contamination  Never use the same media bottle for different cell lines. If caps are dropped or bottles touched unconditionally touched, replace them with new ones  Necks of glass bottles prefer heat at least for 60 secs at a temperature of 200 C  Switch on the laminar flow cabinet 20 mins prior to start working  Cell cultures which are frequently used should be subculture & stored as duplicate strains. THE END.