Team:Warsaw/Cytotoxicity

From 2013.igem.org

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The neurotoxic effects of acrylamide have been widely known for many years. Local symptoms of acrylamide poisoning such as mucous membranes and skin irritation have been formerly reported. There exists also systemic effect characterized by fatigue, sleepiness and memory difficulties; in extreme cases also hallucination, disorientation and confusion.  
+
{{:Team:Warsaw/Templates/StandardPageBegin|Cytotoxicity study}}
 +
__TOC__
 +
==Overview==
 +
The neurotoxic effects of acrylamide have been widely known for many years. Local symptoms of acrylamide poisoning such as mucous membrane and skin irritation have been formerly reported. There also exists a systemic effect characterized by fatigue, sleepiness and memory difficulties; in extreme cases also hallucination, disorientation and confusion were observed.  
 +
[[File:Hela_24_4mM_2.png|255px|thumb|left|alt=A|HeLa cells after 24h incubation with 4mM acrylamide.]]
-
While acrylamide was perceived as severe neurotoxin, there had long not been enough studies on it’s possible carcinogenicity. Yet, the resent studies have showed that acrylamide may also be engaged in that kind of processes.
 
-
Due to the rapid development of plastic industry, acrylamide is becoming to be even more widely present in our environment. But the manufacturing is not the only way, that acrylamide appears in our proximity. Because of Maillard reaction taking place while deep-frying or baking between an amino acid and a reducing sugar, acrylamide comes into being.
 
 +
While acrylamide was perceived as a severe neurotoxin, there had long not been enough studies on its possible carcinogenicity. Yet, the recent research have shown that acrylamide may be engaged in processes.
 +
Due to the rapid development of the plastic industry, acrylamide is becoming even more widely present in our environment. But the manufacturing area is not the only way by which acrylamide appears in our proximity. While deep-frying or baking, through a chemical reaction between an amino acid and a reducing sugar (called the Maillard reaction), acrylamide is formed.
-
Possible ways of absorption of acrylamide are as follows: inhalation, ingestion, and through the skin and mucous membranes. Basing on a report of WHO from 2002 average daily intake for the general population ranges from 0.3 to 0.8 microgram of acrylamide per kilogram of body weight.  
+
Possible ways of acrylamide absorption are as follows: inhalation, ingestion, and through the skin and mucous membranes. Basing on a report of WHO from 2002 average daily intake for the general population ranges from 0.3 to 0.8 micrograms of acrylamide per kilogram of body mass.  
-
Increased consumption of deep-fried food and, following on from that, increased intake of acrylamide, may have serious health consequences. Recent studies have revealed that there exists an association between consumption of deep-fried foods and increased prostate cancer risk.What is also suggested, is that there is a weak positive correlation between increased acrylamide intake and increased possibility of occurrence of endometrial and ovarian cancer.2
+
Increased consumption of deep-fried food and, subsequently, increased intake of acrylamide, may have serious health consequences. Recent studies have revealed an association between consumption of deep-fried foods and increased prostate cancer risk. What is also suggested, is that there is positive correlation between acrylamide intake and increased risk of endometrial and ovarian cancer.  
 +
Considering the alarming effects of acrylamide exposure, we have decided to include in our project a cytotoxicity  study. Our aim is to show how acrylamide may affect various cell lines originating from different tissues. In our experiments we are working on HeLa, 293 and 143B cell lines representing cervical cancer, human embryonic kidney and bone osteosarcoma cells respectively.
-
Considering the alarming effects of the acrylamide exposure, we have decided to enclose to our project cytotoxity and genotoxity study. Our aim is to show how acrylamide may affect different tissues reflected by the cell lines derived from that tissues. In our experiments we would work on Hela and HEK cell lines representing ovarian and kidney cancer cells respectively.  
+
[[File:Alamar1.JPG|250 px|thumb|right|alt=A|Probes for AlamarBlue.]]
-
To conduct our experiments we would implement following methods: Flow cytometry, Hoechst dyeing, Alamar Blue assay, and Micronuclei test.
 
 +
In our experiments we are implementing the following methods: Flow Cytometry, AlamarBlue assay, Cell Growth Assay, Cell Cycle assay and Caspase activity assay.
-
Using flow cytometry we would be enabled to conduct precise analysis of chemical and physical parameters simultaneously. The measurement bases on cell sorting and cell counting according to chosen parameters. (…)
+
To indicate cell viability, we have decided to implement the Alamar Blue assay. It bases on the ability of living cells to convert nonfluorescent resazurin to the highly fluorescent molecule - resorufin. While entering the cells, resazurin is being reduced to resorufin and the bright, red fluorescence is observed. Viable cells are continuing to convert resazurin to resorufin, so the fluorescence intensity increases proportionally, which can be use to measure viability of the cells.
-
In order to be able to examine cell’s nuclei morphology we introduced staining with Hoechst dye. The dye binds to the minor groove of dsDNA preferentially to sequences rich in adenine and thymine. As the Hoechst dye may be excited by ultraviolet light and then emits blue fluorescent light we’ll be able to observe changes in the cell’s nuclei using fluorescent microscopy. As UV light is harmful for the cells, they have to be fixed first in order to avoid excess death during the assay. Our aim is to study changes that occurred due to treating cells with the acrylamide: cell division, cell apoptosis and amount of micronuclei.
+
[[File:Alamar2.JPG|190px|thumb|left|alt=A|Probes for Flow Cytometry]]
 +
Flow cytometry enables us to conduct more precise analysis of chosen aspects of cell biology. After conducting flow cytometry, we will be able to state whether treated cells are undergoing apoptosis, necrosis or if the observed metabolic effects are only cytostatic. 
-
To indicate cell viability, we have decided to implement Alamar Blue assay. It bases on the ability of living cells to convert nonfluorescent resazurin to the highly fluorescent molecule- resorufin. While entering the cells, resazurin is being reduced to resorufin and the bright, red fluorescence is to be observed. Viable cells are continuing to convert resazurin to resorufin, so the strength of fluorescence increases proportionally and may be used to measure viability of the cells.
+
In order to state how acrylamide may influence the progression of cell cycle we have decided to implement Cell Cycle Assay. This method employs flow cytometry to mesure number of cells in a given phase of the cell cycle. Permeabilization of cells with cold ethanol and addition of propidium iodide (PI) prior to analysis, allows us to measure the fluorescence. PI binds to DNA quantitatively so the fluorescence intensity of the stained cells is correlated with the amount of their DNA. Thus, basing on the quantity of DNA we are enabled to assign cells to different cell cycle phases.  
 +
We expect to observe the cytotoxic effects in higher acrylamide concentrations i.e. 3-5 mM. In lower concentrations <1 mM may occur the elimination of the toxicant, whose effects are to be examined.
-
As we would like to measure the genotoxity of acrylamide, we’ve decided to implement micronucleus assay. This test belongs to the most popular and widely used methods of searching for potentially mutagenic substances. The assay bases on formation of the micronuclei, which are the erratic nuclei formed during the anaphase due to mutagen exposition. They may originate both from acentric chromosome fragments or whole chromosomes unable to migrate properly. The modifications in chromosomes structure, observed during the test, indicate the genotoxic effect of tested substance.
+
==Results==
 +
After conducting our experiments we have obtained following results:
 +
* loss of metabolic activity (results obtained from AlamarBlue assay)
 +
* induction of apoptotic cell death (stated by the presence of annexinV positive cells and the observation of caspase activity)
 +
* suppression of cell growth and proliferation (stated on the basis of Cell Growth assay and AlamarBlue assay)
 +
* disturbances in the cell cycle (based on the outcomes of Cell Cycle assay)
-
In our study we would search for optimal acrylamide concentration for particular cell line in order to conduct the experiments. We expect to observing the cytotoxic effects in higher acrylamide concentrations i.e. 3-5 mM. In lower concentrations 1-2 mM may occur the elimination of the toxicant, which is to be examined.
+
==Getting the experiments underway==
 +
As a starting point for our experiments we have decided to implement AlamarBlue assay. It bases on the ability of living cells to convert nonfluorescent resazurin to the highly fluorescent molecule- resorufin. While entering the cells, resazurin is being reduced to resorufin and the bright, red fluorescence is observed. Viable cells are continuing to convert resazurin to resorufin, so the fluorescence intensity increases proportionally and can be use to measure viability of the cells. AlamarBlue assay provides reliable and repeatable results yet is easy to conduct thus it serves as a trustworthy basis for further research.
-
Bibliography:  
+
In order to obtain reliable results of experiments we have decided to conduct preliminary assays to determine plating density and concentration of acrylamide for each cell line: HeLa, 293 and 143B. The protocol of the assay as well as detailed conduct can be found in the section: Extras.
 +
 +
The outcome of AlamarBlue assay showed the existence of strong, negative correlation between acrylamide exposure and cell viability (Figure 1.). So the longer exposure time and the higher concentration of acrylamide, the weaker the cell viability.
-
1. Stott-Miller M, Neuhouser ML, Stanford JL; Consumption of deep-fried foods and risk of prostate cancer; Epub 2013 Jan 17.
+
[[File:avHEK2.png|550px|center|frameless|border|alt=A|Figure 1. Influence of acrylamide on 293 cells viability. Cells were treated with various concentration of acrylamide and the viability was measured after indicated period of time.|]]
-
2. Ehlers A, Lenze D, Broll H, Zagon J, Hummel M, Lampen A; Dose dependent molecular effects of acrylamide and glycidamide in human cancer cell lines and human primary hepatocytes; Epub 2012 Dec 31
+
In order to state whether the loss of cell viability, that we have observed, was caused by decrease in cell division (the cytostatic effect of acrylamide) or by cell death (the cytotoxic effect of acrylamide) we have implemented Cell growth assays.  To conduct the assays we have seeded cells from different cell lines (HeLa, 293 and 143B) in 6-wells plates adding proper concentration of acrylamide to each well and counted the amount of cells in counting chamber after trypan blue staining, for 24, 48 and 72 hours incubation. This approach indicated that acrylamide treatment affects cell proliferation and induces cell death.
-
3. Ahmad Besaratinia_ and Gerd P.Pfeifer; A review of mechanisms of acrylamide carcinogenicity; Carcinogenesis vol.28 no.3 pp.519–528, 2007
+
[[File:CG2HeLa.png|center|frameless|border|caption|850px]]
-
4. O'Brien J, Wilson I, Orton T, Pognan F; Investigation of the Alamar Blue (resazurin) fluorescent dye for the assessment of mammalian cell cytotoxicity; Eur J Biochem. 2000 Sep;267(17):5421-6.
+
[[File:CGA-HeLa.png|center|frameless|border|caption|550px]]
-
5. Naoki Koyamaa,b,c, Hiroko Sakamoto a, Mayumi Sakuraba a, Tomoko Koizumi a,
+
In order to bring under scrutiny changes in the cell cycle we have carried out Cell Cycle assay. We observed that there occur disturbances in the cell cycle depending on concentration of acrylamide and incubation time.
-
Yoshio Takashima a, Makoto Hayashi a, Hiroshi Matsufuji b, Kazuo Yamagata b,
+
 
-
Shuichi Masudac, Naohide Kinae c, Masamitsu Honmaa,; Genotoxicity of acrylamide and glycidamide
+
<gallery widths=800px heights=400px perrow=1 caption="Histograms for Cell Cycle assay">
-
in human lymphoblastoid TK6 cells; Mutation Research 603 (2006) 151–158
+
 
 +
 
 +
File:HeLa-hist.png|HeLa cell line upper row: 24h incubation bottom row: 48h incubation acrylamide concentrations from left: NC, 1mM, 3mM, 5mM
 +
 
 +
File:143B-hist.png|143B cell line upper row: 24h incubation bottom row: 48h incubation acrylamide concentrations from left: NC, 1mM, 2mM, 5mM
 +
 
 +
File:HEK293-hist.png|HEK293 cell line upper row: 24h incubation bottom row: 48h incubation acrylamide concentrations from left: NC, 1mM, 3mM, 5mM
 +
 
 +
 
 +
</gallery>
 +
 
 +
<html>
 +
These results made us to consider further investigation. As we wanted to state whether acrylamide induces apoptotic cell death we decided to measure caspase activity and examine presence of the cells that would bind annexin V (which are hallmarks of apoptosis).
 +
<a href="http://pl.promega.com/products/cell-health-and-metabolism/apoptosis-assays/luminescent-caspase-assays/caspase_glo-3_7-assay-systems/?origUrl=http%3a%2f%2fwww.promega.com%2fproducts%2fcell-health-and-metabolism%2fapoptosis-assays%2fluminescent-caspase-assays%2fcaspase_glo-3_7-assay-systems%2f" target="_blank">Caspase-Glo 3/7 Assay</a> revealed that there is an increase in caspase activity caused by acrylamide treatment.
 +
The Flow Cytometry analysis showed that there is a growth in annexin V positive cells number due to addition of acrylamide.
 +
 
 +
 
 +
</html>
 +
 
 +
[[File:caspase1.png|center|frameless|border|caption|450px]]
 +
 
 +
 
 +
<gallery widths=800px heights=400px perrow=1 caption="Figures for the Flow Cytometry">
 +
 
 +
 
 +
File:HeLa-FC.png|HeLa cell line upper row: 24h incubation bottom row: 48h incubation acrylamide concentrations from left: NC, 1mM, 3mM, 5mM
 +
 
 +
File:143B-FC.png|143B cell line upper row: 24h incubation bottom row: 48h incubation acrylamide concentrations from left: NC, 1mM, 2mM, 5mM
 +
 
 +
File:HEK-FC.png|HEK293 cell line upper row: 24h incubation bottom row: 48h incubation acrylamide concentrations from left: NC, 1mM, 3mM, 5mM
 +
 
 +
</gallery>
 +
 
 +
In our study we've included Cisplatin control, whose results are to be seen in section:  [https://2013.igem.org/Team:Warsaw/Notebook Notebook]
 +
 
 +
All of the results as well as graphs, figures and statistics are to be seen in section: [https://2013.igem.org/Team:Warsaw/Cellular_biology_lab_journal Cellular biology lab journal]
 +
 
 +
==Summary==
 +
 
 +
Despite the fact that it is impossible to relate directly the results obtained for the cell lines to human organism, it may give a basis for further examination and extended research. In our experiments '''we showed the existence of cytotoxic and cytostatic effect of acrylamide on HeLa, 143B and 293 cell lines. We also found a correlation between time of exposure to acrylamide and the decrease in cell viability and proliferation.'''
 +
 
 +
By carrying out our cytotoxicity study '''we would like to emphasize the importance of synthetic biology research'''. After showing the possible harmful effects of acrylamide we aimed to reveal how products of synthetic biology may influence and facilitate our everyday life. We also tried to raise the awareness of the threats connected with the consumption of tertiary processed foods.
 +
 
 +
Finally, let us make you imagine that you are able to check the amount of acrylamide before eating your chips. With our FluoSafe sensor it will be soon possible.
 +
 
 +
 
 +
'''Bibliography:'''
 +
# Stott-Miller, M., Neuhouser, ML. & Stanford, JL. Consumption of deep-fried foods and risk of prostate cancer. Epub (2013).
 +
# Ehlers, A., Lenze, D., Broll, H., Zagon, J., Hummel, M. & Lampen, A. Dose dependent molecular effects of acrylamide and glycidamide in human cancer cell lines and human primary hepatocytes. Epub (2012).
 +
# Besaratinia, A. & Pfeifer, GP. A review of mechanisms of acrylamide carcinogenicity. Carcinogenesis 28, 519–528 (2007).
 +
# O'Brien, J., Wilson, I., Orton, T. & Pognan, F. Investigation of the Alamar Blue (resazurin) fluorescent dye for the assessment of mammalian cell cytotoxicity. Eur J Biochem 28. 5421-6 (2000).
 +
# Koyamaa, N., Sakamoto, H., Sakuraba, M., Koizumi, T., Takashima, Y., Hayashi, M., Matsufuji, H., Yamagata, K., Masudac, S., Kinae, S. & Honmaa M. Genotoxicity of acrylamide and glycidamide in human lymphoblastoid TK6 cells. Mutation Research 603, 151–158 (2006).
 +
 
 +
{{:Team:Warsaw/Templates/StandardPageEnd}}

Latest revision as of 00:11, 5 October 2013

Cytotoxicity study

Contents

Overview

The neurotoxic effects of acrylamide have been widely known for many years. Local symptoms of acrylamide poisoning such as mucous membrane and skin irritation have been formerly reported. There also exists a systemic effect characterized by fatigue, sleepiness and memory difficulties; in extreme cases also hallucination, disorientation and confusion were observed.

A
HeLa cells after 24h incubation with 4mM acrylamide.


While acrylamide was perceived as a severe neurotoxin, there had long not been enough studies on its possible carcinogenicity. Yet, the recent research have shown that acrylamide may be engaged in processes. Due to the rapid development of the plastic industry, acrylamide is becoming even more widely present in our environment. But the manufacturing area is not the only way by which acrylamide appears in our proximity. While deep-frying or baking, through a chemical reaction between an amino acid and a reducing sugar (called the Maillard reaction), acrylamide is formed.

Possible ways of acrylamide absorption are as follows: inhalation, ingestion, and through the skin and mucous membranes. Basing on a report of WHO from 2002 average daily intake for the general population ranges from 0.3 to 0.8 micrograms of acrylamide per kilogram of body mass.


Increased consumption of deep-fried food and, subsequently, increased intake of acrylamide, may have serious health consequences. Recent studies have revealed an association between consumption of deep-fried foods and increased prostate cancer risk. What is also suggested, is that there is positive correlation between acrylamide intake and increased risk of endometrial and ovarian cancer.

Considering the alarming effects of acrylamide exposure, we have decided to include in our project a cytotoxicity study. Our aim is to show how acrylamide may affect various cell lines originating from different tissues. In our experiments we are working on HeLa, 293 and 143B cell lines representing cervical cancer, human embryonic kidney and bone osteosarcoma cells respectively.

A
Probes for AlamarBlue.


In our experiments we are implementing the following methods: Flow Cytometry, AlamarBlue assay, Cell Growth Assay, Cell Cycle assay and Caspase activity assay.

To indicate cell viability, we have decided to implement the Alamar Blue assay. It bases on the ability of living cells to convert nonfluorescent resazurin to the highly fluorescent molecule - resorufin. While entering the cells, resazurin is being reduced to resorufin and the bright, red fluorescence is observed. Viable cells are continuing to convert resazurin to resorufin, so the fluorescence intensity increases proportionally, which can be use to measure viability of the cells.


A
Probes for Flow Cytometry

Flow cytometry enables us to conduct more precise analysis of chosen aspects of cell biology. After conducting flow cytometry, we will be able to state whether treated cells are undergoing apoptosis, necrosis or if the observed metabolic effects are only cytostatic.

In order to state how acrylamide may influence the progression of cell cycle we have decided to implement Cell Cycle Assay. This method employs flow cytometry to mesure number of cells in a given phase of the cell cycle. Permeabilization of cells with cold ethanol and addition of propidium iodide (PI) prior to analysis, allows us to measure the fluorescence. PI binds to DNA quantitatively so the fluorescence intensity of the stained cells is correlated with the amount of their DNA. Thus, basing on the quantity of DNA we are enabled to assign cells to different cell cycle phases.

We expect to observe the cytotoxic effects in higher acrylamide concentrations i.e. 3-5 mM. In lower concentrations <1 mM may occur the elimination of the toxicant, whose effects are to be examined.

Results

After conducting our experiments we have obtained following results:

  • loss of metabolic activity (results obtained from AlamarBlue assay)
  • induction of apoptotic cell death (stated by the presence of annexinV positive cells and the observation of caspase activity)
  • suppression of cell growth and proliferation (stated on the basis of Cell Growth assay and AlamarBlue assay)
  • disturbances in the cell cycle (based on the outcomes of Cell Cycle assay)

Getting the experiments underway

As a starting point for our experiments we have decided to implement AlamarBlue assay. It bases on the ability of living cells to convert nonfluorescent resazurin to the highly fluorescent molecule- resorufin. While entering the cells, resazurin is being reduced to resorufin and the bright, red fluorescence is observed. Viable cells are continuing to convert resazurin to resorufin, so the fluorescence intensity increases proportionally and can be use to measure viability of the cells. AlamarBlue assay provides reliable and repeatable results yet is easy to conduct thus it serves as a trustworthy basis for further research.

In order to obtain reliable results of experiments we have decided to conduct preliminary assays to determine plating density and concentration of acrylamide for each cell line: HeLa, 293 and 143B. The protocol of the assay as well as detailed conduct can be found in the section: Extras.

The outcome of AlamarBlue assay showed the existence of strong, negative correlation between acrylamide exposure and cell viability (Figure 1.). So the longer exposure time and the higher concentration of acrylamide, the weaker the cell viability.

A

In order to state whether the loss of cell viability, that we have observed, was caused by decrease in cell division (the cytostatic effect of acrylamide) or by cell death (the cytotoxic effect of acrylamide) we have implemented Cell growth assays. To conduct the assays we have seeded cells from different cell lines (HeLa, 293 and 143B) in 6-wells plates adding proper concentration of acrylamide to each well and counted the amount of cells in counting chamber after trypan blue staining, for 24, 48 and 72 hours incubation. This approach indicated that acrylamide treatment affects cell proliferation and induces cell death.

caption
caption

In order to bring under scrutiny changes in the cell cycle we have carried out Cell Cycle assay. We observed that there occur disturbances in the cell cycle depending on concentration of acrylamide and incubation time.

These results made us to consider further investigation. As we wanted to state whether acrylamide induces apoptotic cell death we decided to measure caspase activity and examine presence of the cells that would bind annexin V (which are hallmarks of apoptosis). Caspase-Glo 3/7 Assay revealed that there is an increase in caspase activity caused by acrylamide treatment. The Flow Cytometry analysis showed that there is a growth in annexin V positive cells number due to addition of acrylamide.

caption


In our study we've included Cisplatin control, whose results are to be seen in section: Notebook

All of the results as well as graphs, figures and statistics are to be seen in section: Cellular biology lab journal

Summary

Despite the fact that it is impossible to relate directly the results obtained for the cell lines to human organism, it may give a basis for further examination and extended research. In our experiments we showed the existence of cytotoxic and cytostatic effect of acrylamide on HeLa, 143B and 293 cell lines. We also found a correlation between time of exposure to acrylamide and the decrease in cell viability and proliferation.

By carrying out our cytotoxicity study we would like to emphasize the importance of synthetic biology research. After showing the possible harmful effects of acrylamide we aimed to reveal how products of synthetic biology may influence and facilitate our everyday life. We also tried to raise the awareness of the threats connected with the consumption of tertiary processed foods.

Finally, let us make you imagine that you are able to check the amount of acrylamide before eating your chips. With our FluoSafe sensor it will be soon possible.


Bibliography:

  1. Stott-Miller, M., Neuhouser, ML. & Stanford, JL. Consumption of deep-fried foods and risk of prostate cancer. Epub (2013).
  2. Ehlers, A., Lenze, D., Broll, H., Zagon, J., Hummel, M. & Lampen, A. Dose dependent molecular effects of acrylamide and glycidamide in human cancer cell lines and human primary hepatocytes. Epub (2012).
  3. Besaratinia, A. & Pfeifer, GP. A review of mechanisms of acrylamide carcinogenicity. Carcinogenesis 28, 519–528 (2007).
  4. O'Brien, J., Wilson, I., Orton, T. & Pognan, F. Investigation of the Alamar Blue (resazurin) fluorescent dye for the assessment of mammalian cell cytotoxicity. Eur J Biochem 28. 5421-6 (2000).
  5. Koyamaa, N., Sakamoto, H., Sakuraba, M., Koizumi, T., Takashima, Y., Hayashi, M., Matsufuji, H., Yamagata, K., Masudac, S., Kinae, S. & Honmaa M. Genotoxicity of acrylamide and glycidamide in human lymphoblastoid TK6 cells. Mutation Research 603, 151–158 (2006).