1、Journal of Visualized ECopyright 2011 Journal of Visualized ExperimentsAugust 2011|54|e2899|Page 1 of 4Video ArticleInduction and Testing of Hypoxia in Cell CultureDanli Wu1,Patricia Yotnda11Center for Cell and Gene Therapy,Baylor College of MedicineCorrespondence to:Patricia Yotnda at pyotndabcm.ed
2、uURL:http:/ Biology,Issue 54,mammalian cell,hypoxia,anoxia,hypoxia inducible factor(HIF),reoxygenation,normoxiaDate Published:8/12/2011Citation:Wu,D.,Yotnda,P.Induction and Testing of Hypoxia in Cell Culture.J.Vis.Exp.(54),e2899,doi:10.3791/2899(2011).AbstractHypoxia is defined as the reduction or l
3、ack of oxygen in organs,tissues,or cells.This decrease of oxygen tension can be due to a reducedsupply in oxygen(causes include insufficient blood vessel network,defective blood vessel,and anemia)or to an increased consumption ofoxygen relative to the supply(caused by a sudden higher cell proliferat
4、ion rate).Hypoxia can be physiologic or pathologic such as in solidcancers 1-3,rheumatoid arthritis,atherosclerosis etc Each tissues and cells have a different ability to adapt to this new condition.Duringhypoxia,hypoxia inducible factor alpha(HIF)is stabilized and regulates various genes such as th
5、ose involved in angiogenesis or transport ofoxygen 4.The stabilization of this protein is a hallmark of hypoxia,therefore detecting HIF is routinely used to screen for hypoxia 5-7.In this article,we propose two simple methods to induce hypoxia in mammalian cell cultures and simple tests to evaluate
6、the hypoxic status ofthese cells.Video LinkThe video component of this article can be found at http:/ induced by CoCl2 solutionCobalt(II)Chloride hexahydrate(CoCl2 6H2O,MW=237.9)is a chemical inducer of hypoxia-inducible factor-1.3 8.This product is soluble inwater(100 mg/ml),yielding a clear,red so
7、lution.1.Prepare a 25mM stock solution in sterile dd water,(prepare immediately before use)2.Use CoCl2 at the final concentration of 100M in your regular cell culture media to induce hypoxia.3.Add the CoCl2 containing media to your cells and incubate the cultures for 24hours in a conventional incuba
8、tor(37C;5%C02).The above concentration works for the cell lines we have tested but each cell line should be tested at various concentrations(to establish adose-dependent curve)as well as at various incubation times in order to limit drug related toxicity and optimize the assay.2.Hypoxia induced in M
9、odular Incubator Chamber1.Prepare at least two identical(twin culture)cell cultures.Cell cultures can be in Flasks,plates or culture dishes.To open the chamber,firstopen the two white plastic clamps located on the tubes attached to the chamber(tubes used for the injection/purging the hypoxic gas)and
10、gently open the steel ring clamp.2.Release the clamp.The lid and trays can now be removed.3.Place the cell culture in the hypoxic chamber.Also place a Petri dish containing sterile water in the chamber to provide adequatehumidification of the cultures.4.Place the twin cell culture in normoxia as con
11、trol.5.Make sure your trays are secured and not moving,and then close the chamber with its lid.Correctly position the steel ring clamp to ensurethe hermetical closure of the chamber and close it.6.To create hypoxia,attach the tubing to a hypoxia tank containing a 1%O2 gas mixture.If you have a flow
12、meter connected to your tank yourchamber will be directly connected to it(gas tank-flow meter chamber).We use a flow meter incorporated in our regulator.7.It is important to remove most if not all oxygen present in the chamber and in your media,to do so flush the chamber by opening the gas tankat a
13、flow rate of 20 liters per minutes for 7-10 minutes;then quickly turn off the gas flow and completely close the chamber by closing bothwhite clamps.8.Return the chamber to a conventional incubator for the desired period of time.If you use large cultures,allow media in cultures to de-gas for1-2 hours
14、 and then repeat flush.Journal of Visualized ECopyright 2011 Journal of Visualized ExperimentsAugust 2011|54|e2899|Page 2 of 4The above steps are based on the constructor recommendations(Billups-Rothenberg,Inc).Make sure you gas tank are properly secured atall time.Notes:In order to eliminate the O2
15、 contained in the media it is advised to re-gas the chamber once after 1-3hours.For incubation time longer than 48hours it is also advised to re-gas the chamber.Oxygen sensors(electrodes/manometer)that allow measurements of the O2 contained in cells/chamber will provide a more precisemeasurement of
16、the intracellular/chamber O2 contain).Culturing cells at various time lengths to make a time-curve would help determine the optimal time expression of HIF-1 in your particularcells.3.Evaluation of Hypoxia1.HIF-1 detection by western blot.1.Re-open your chamber as described in section 2.2 and immedia
17、tely place your cultures on ice.2.Lyse hypoxia treated and non-treated cells with 5%SDS solution in the plates then transfer the cell lyzate to tubes,sonicate,spindownthe cell debris and collect the supernatant.3.Measure protein concentration using BCA kit,prepare sample by adding loading buffer and
18、 heating at 95C for 5 min.4.Electrophorese proteins on an 8%SDS-polyacrylamide gel and transfer to Nitrocellulose membranes.5.Block the membrane in PBS containing 5%non-fat dry milk and 0.1%Tween 20 at room temperature for 1 hour or at 4C overnight onshaker.6.Immunoblot overnight with anti-HIF-1 pri
19、mary monoclonal antibody(1/600)in the same buffer at 4 C.7.Wash 3 times in PBS containing 0.1%Tween 20 at room temperature,5min each time and incubate with HRP-secondary antibody(1/2000)in PBS+0.1%Tween 20 for 45 min.8.Wash 3 times in PBS containing 0.1%Tween 20 at room temperature,5min/time.9.Use P
20、ierce ECL kit and X-ray film to show the protein band2.Hypoxia Responsive Element(HRE).HIF-1 regulates numerous genes(i.e VEGF,EPO)by binding to a sequence called Hypoxia Regulating Element(HRE).Using HREassociated to a marker gene it is possible to detect HIF activity 9.To use this method,first you
21、 need to transfect your cells with a HRE-luciferase plasmid using a transfection method adapted to your cells.For example we used Lipofectamine 2000.Cells need to be transfectedat least 4 hours before to be incubated in hypoxia and normoxia.This time allows the DNA to enter the cells so that this fi
22、rst step is notaffected by hypoxia.The luciferase signal is detected using a Luciferase Assay Kit.1.Incubate your HRE-transfected cells in hypoxia in modular chamber or use HRE-transfected cells incubated with CoCl2,include anormoxia control.2.After the desired incubation period,remove growth medium
23、 from cells.3.Rinse cells in PBS,remove the PBS.4.Dispense 400l 1X lysis reagent into culture dish and scrape the attached cells,then transfer them to a micro tube.5.Pellet debris by brief centrifugation.6.Mix 20l of cell lysates supernatant with 100l of Luciferase Assay Reagent and measure the lumi
24、nescence using a luminometer.4.Representative Results:In K562 cells(human leukemia cell line)cultured 2 days in low oxygen,compared to normoxia,hypoxia induces an increase of HIF-1 proteinthat was detected by western blot(Figure 1).Using HRE-luciferase modified 293 cells(embryonic kidney cell line)c
25、ultured in hypoxia,a significant increased of HIF-1 activity was detectedin hypoxic cells(Figure 2).Journal of Visualized ECopyright 2011 Journal of Visualized ExperimentsAugust 2011|54|e2899|Page 3 of 4Figure 1:Increase HIF-1 in hypoxic cells.K562 cells were culture in normoxia and hypoxia(hypoxic
26、chamber)for 48 hrs and analyzed bywestern blot using an antibody specific for HIF-1.An antibody specific for actin was used for the loading control.Figure2:HIF-1 activity.HRE-luciferase modified 293 cells were cultured in hypoxia and normoxia for 48 hrs and then lysed to detect luciferasesignal usin
27、g a luciferase assay kit and a luminometer.Results are expressed as the relative luminescence unit(RLU).DiscussionCell proliferation and viability in hypoxic conditions vary a lot depending on the cell types.Therefore,you should adjust the cell number or thenumber of cultures plates you start with t
28、o make sure you will have enough cells/proteins for your experiments.The Cobalt Chloride method has the advantage to be inexpensive and fast.This product mimics hypoxia by inducing HIF-1/3 but can alsoregulate other genes,make sure this product is adapted to your project by checking what other effec
29、ts it could have on the function andphenotype of your particular cells independently of the mimic-hypoxic effect.Another drug also used to mimic hypoxia is Deferoxaminemesylate(DFO,used at 100 M final concentration).The use of these drugs allows the experimentator to open the culture plate/dish/flas
30、k manytimes without affecting the hypoxic condition.The level of oxygen contained in the gas mixture can vary depending on your experiments and cell types as hypoxia values vary dependingon the tissues and cell types.Indeed,some cells are hypoxic in 5%O2 other need less than 1%O2 to be hypoxic.5%CO2
31、 is added to the gasmixture to stabilize the pH of the cultures,the rest of the gas is usually Nitrogen.Hypoxic chambers have the advantage of not using drugs that can alternate cell behavior independently of the oxygen tension.However,notall types of experimentation can be done as oxygen re-enters
32、the chamber at each opening and thus lessens hypoxia.You should considerthis factor in your experiments;hypoxia/re-oxygenation is a specific condition that can affect some cell types.An alternative is to use hypoxiaworkstations(connected to pre-mixed gas tanks or to gas mixing systems)or larger hypo
33、xia incubator(hypoxia processing chamber with glovebox)that allows the experimentation to change media and manipulate cells in continuous hypoxic environment.Various hypoxic chambershave been commercialized over the past decade and should be chosen according to your laboratory used,projects,space,si
34、ze,and budget.Always ensure the good use and condition of your chamber to guarantee correct culture conditions.In general when using a chamber,the levelof hypoxia can be modulated by selecting the various gas mixes(i.e.1%,5%10%oxygen).Regarding the detection of HIF-1,it is important to know that som
35、e cancer cell line express HIF-1 in normoxia.It is therefore critical to use anormoxia-control to determine the basal level of HIF in these cell lines.HIF-1 can also be present in normoxia in non-malignant cells followingcell stimulation or stress.This could also occur if these cells are starved,mak
36、e sure your cell cultures are properly feed and maintained.DisclosuresNo conflicts of interest declared.Journal of Visualized ECopyright 2011 Journal of Visualized ExperimentsAugust 2011|54|e2899|Page 4 of 4References1.Swinson,D.E.&OByrne,K.J.Interactions between hypoxia and epidermal growth factor
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39、Tatum,J.L.,et al.Hypoxia:importance in tumor biology,noninvasive measurement by imaging,and value of its measurement in themanagement of cancer therapy.Int J Radiat Biol.82(10),699-757(2006).7.Brahimi-Horn,M.C.&Pouyssegur,J.HIF at a glance.J Cell Sci.122(Pt 8),1055-1057(2009).8.Piret,J.P.,Mottet,D.,
40、Raes,M.,&Michiels,C.CoCl2,a chemical inducer of hypoxia-inducible factor-1,and hypoxia reduce apoptotic celldeath in hepatoma cell line HepG2.Ann N Y Acad Sci.973,443-447(2002).9.Emerling,B.M.,Weinberg,F.,Liu,J.L.,Mak,T.W.,&Chandel,N.S.PTEN regulates p300-dependent hypoxia-inducible factor 1 transcriptionalactivity through Forkhead transcription factor 3a(FOXO3a).Proc Natl Acad Sci U S A.105(7),2622-2627(2008).
