Hello Steemians, hope you are all having a very productive week and can hardly wait for weekend to come ;) For some time already I've been thinking about starting a section in my blog which would be dedicated to daily challenges all scientists encounter while working in the lab, including myself. The idea is to talk about how it's like to be scientist in real life (definitely not like in movies or CSI series!) and to describe typical and atypical days in a cancer research lab. ![20180116_122241 copy.jpg](https://steemitimages.com/DQmZjcZotG492scdJXphhgGeY6qqbWWXGMVywBK5pr8Z6tg/20180116_122241%20copy.jpg) *Don't be afraid, that's just me, no make-up, all natural :)* Today I will introduce you to cell culturing and importance of using cell lines as model system in research. ### Cell culture - what is that? ------------------------- By definition, cell culture represents removal of cells from an animal or plant and their subsequent growth in an artificial environment which mimics conditions of the natural environment (organism) they derive from. Distinction can be made between **primary cultures**, where cells are isolated directly from the tissue and proliferated until they reach confluence (cell density at which no further growth is possible), and **cell lines**, which are established after the first subculture of primary cultures. Cell lines can be **finite**, which means they have limited life span (usually ones derives from primary cultures and normal cells) and **continuous cell lines**, meaning that those cells became immortal though a process called transformation. Cancer cell lines are the example of continuous cell lines, which are the cell lines I'm working with (more precisely - human cancer cell lines) and I will talk about them in more detail. ### How do we grow them? ------------------ Cell lines are usually grown in culture flasks, that look like this: ![20180116_122103 copy.jpg](https://steemitimages.com/DQmaZCQwMYpTYiDcKbrJPAhXhyuzFU7J1PC9VAXP8e9Loqh/20180116_122103%20copy.jpg) Culture flasks are filled with growth media, which provide all the nutrients (when supplemented with serum) required for cell survival and growth. There are different types of growth media, because different cell types have different needs regarding nutrients. For example, typical growth medium called Roswell Park Memorial Institute (RPMI or RPMI 1640) contains glucose, salts, amino acids, vitamins and pH indicator (phenol red). **Why do we need a pH indicator in growth media?** It is of great importance to monitor the acidity of growth media, because most mammalian cells grow well at pH 7.4, and too much acidity or alkalinity can kill them. If the media color is orange-red, that means that pH is optimal for cell growth. In case of high confluence of cells or bacterial infection of cell culture, the metabolic products of cell growth increase acidity of media and it becomes yellow. Likewise, when alkalinity of medium increases, it turns its color to purple. **How do we maintain the optimal pH of media in cell culture flasks?** Growth media contains an organic buffer called HEPES or CO₂-bicarbonate based buffer, which buffer the cells in culture against changes in the pH. Changes in atmospheric CO₂ influence the pH of the medium because the pH of the medium is dependent on the balance of dissolved CO₂ and bicarbonate (HCO₃–). This is why it is necessary to maintain levels of exogenous CO₂ constant, and that's done by keeping cell culture flasks in special incubators: ![IMG-a9c71bf842233ad548471a9dd46d0214-V copy.jpg](https://steemitimages.com/DQmPER1dXM3tt23jDpg8ZEF2ZbNV5J3S64v8EkaJ1pyRzGy/IMG-a9c71bf842233ad548471a9dd46d0214-V%20copy.jpg) Moreover, incubators maintain constant temperature that is optimal for cell growth (for human cell lines it is of course 37 ^oC) and high level of humidity, in order to prevent evaporation of media from cell culture dishes. ### What are the lab safety rules we must follow when we work with biological material? ------------------------ In every lab safety comes first! This means that certain rules and measures must be strictly followed to reduce or eliminate exposure of people and the outside environment to potentially harmful biological agents. When it comes to working with cell lines, all manipulation with them is performed in **cell culture hoods**. They are the most important equipment to provide protection of infectious splashes or aerosols to the experimenter, as well as to provide sterile environment for working with cell lines, by having a constant air flow directed to outside of the hood. Personal protective equipment (PPE) serves as immediate barrier between the experimenter and the hazardous agent, and includes items such as gloves, laboratory coats, shoe covers, face shields, safety glasses, etc. On the first picture you saw me wearing the special coat that it's worn only when working in cell culture room (it mustn't be taken outside!) and I also wear gloves that cover my hands and part of the coat sleeves, so that no part of my skin is exposed to potential hazardous agents. Shoe covers should cover your shoes completely and must be put on before entering the cell culture room, and also taken off before leaving it. They protect the cell culturing environment from outside dirt, ans also provide protection for the experimenters and outside environment, keeping the potential spills of hazardous material off their shoes: ![20180116_122443 copy.jpg](https://steemitimages.com/DQmS2NivaxqaXfeS6vQodUiVo3HZnfsrvicjVJcKQmAiPGS/20180116_122443%20copy.jpg) ### Why do we use cell lines in research? ----------------------- Cell lines are irreplaceable tool in modern research, especially when we talk about cancer research. Each experiment we design begins with cancer cell lines, because they are basic model system for studying molecular pathways responsible for cancer development, as well as to study the effect of new drugs with potential anticancer activity. Before we are allowed to proceed to using experimental animals in our research, we must have valid and reproducible results in cell lines. I hope this was interesting read and that you learned something you didn't know before about using cell lines in cancer research. Until next time, relax and keep steemSTEM! ;) ![20180116_122403 manja copy.jpg](https://steemitimages.com/DQmd4c3dPy2otupDLEqJ1AYeXCwg7Wx6gCpkFShkcGnz1i4/20180116_122403%20manja%20copy.jpg) ------------------------ Literature [Cell Culture Basics Handbook](https://www.thermofisher.com/content/dam/LifeTech/global/promotions/global/images/aai-2015/aai-pdfs/GibcoCellCultureBasicsHandbook.pdf) [Cell lines](https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3341241/) [Roswell Park Memorial Institute medium](https://en.wikipedia.org/wiki/Roswell_Park_Memorial_Institute_medium) [pH & CO2 Levels](https://www.thermofisher.com/ng/en/home/references/gibco-cell-culture-basics/cell-culture-environment/ph-co2-levels.html#) [Phenol red](https://en.wikipedia.org/wiki/Phenol_red#Indicator_for_cell_cultures) [CO2 Incubator / Cell Culture Incubator](https://www.labcompare.com/General-Laboratory-Equipment/75-CO2-Incubator-Cell-Culture-Incubator/) ---------------------------------------- #### For more scientific-related content check [steemSTEM](https://steemit.com/trending/steemstem). Follow me if you like my posts and want to read some more ;) If you have any thoughts/suggestions fell free to leave a comment! ![andjelka.jpg](https://steemitimages.com/DQmRFAoQGL2nFNBBqipZd1Bzm1bdmF9HuKGRiYWNmRHcoj2/andjelka.jpg) Image credits: [Jason Brooks](https://www.jason-brooks.com/) and [Prof. Sharona Even-Ram](https://medicine.ekmd.huji.ac.il/En/Publications/ResearchersPages/pages/sharonaev.aspx)

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