Team:SupBiotech-Paris/Tissue targeting

From 2009.igem.org

(Difference between revisions)
(Conclusion)
(Discussion)
Line 67: Line 67:
[[Image : Graphpoumon.png|center|200px|float]]
[[Image : Graphpoumon.png|center|200px|float]]
-
La figure ci-dessus est tiré de la publication « [[Team:SupBiotech-Paris/Bibliography#revulung|Thymus as a target for mycobacterial infections]] ». Le même type de protocole a été réalisé, avec injection de 10^6 CFU/ml de <i>M. avium</i> administré par voie intraveineuse. Il est décrit dans cette figure que les poumons sont infectés dès le premier jour de l’infection, mais en très petite quantité (légèrement supérieur à 10^1, puis de manière prolongée avec une propagation rapide (de 10^1 à 10^6 CFU/organe en moins de 5 semaines). Ceci prouve donc bien que les poumons sont colonisé par <i>M. avium</i>.<br>
+
The above figure is extracted from the publication « [[Team:SupBiotech-Paris/Bibliographie#revulung|Thymus as a target for mycobacterial infections]] ». A similar protocol was performed with injection of 10 ^ 6 CFU / ml <i> M. <i> avium </i> administered intravenously. . It is described in this figure that the lungs are infected from the first day of infection, but in very small amount (just over 10 ^ 1, then it is more prolonged with the rapid spread (10 ^ 1 to 10 ^ 6 CFU / organ in less than 5 weeks). This proves, therefore, that the lungs are colonized by  M.<i> avium </i>.<br>

Revision as of 00:59, 21 October 2009

framless


Contents

Tissue targeting

Context

The non-small cell lung cancer, or NSCLC, is a cancer, which develops in the organ lumen. This tumor localization is essentially due to factors triggering the tumorogenesis (example: tobacco). A logic route of administration for the treatment would be the aerosol route, though a nebulization of the bacteria. But, this route is not the one that we chose for our treatment. The DVS treatment applied to the lungs cancer is administrated by intravenous.

Objective

We decided to check and quantify the mycobacterium avium presence, the tissue vector, in side the lungs, during the intraveinous administration. Thus, we realized an in vivo study in several murine models.


Back to top

Experimental method

To realize the in vivo study , we designed a bioluminescence protocol, which allows the real-time monitoring, of our tissue vector propagation in mice. The bioluminescence is a good reporter system to analyze the mycobacterial implantation and the clearance in vivo. We used a tool kindly provided by Dr Brian D. Robertson (Imperial College London researcher). This tool is a plasmid, once electroporated in M. avium can produce the firefly luciferase, a reporter gene, allowing the monitoring. Indeed, the luciferase catalysis the luciferin oxidation into oxiluciferin, involving photons emission, which can be caught by a CCD camera photosensitive (IVIS, Imaging System 50, Xenogen).
Unfortunately, the growth of electroporated mycobacteria with the monitoring plasmid, was so slow, it was not possible to realize this study within the given time (generation time of M. avium: nearly 20 hours. That is why we decided to change our protocol.
Following this lack of time, we used another protocol (detailed in the following subpart) to check and quantify the presence of our tissue vector in the lung. For this, we studied in the literature what dose of M.avium could be injected into a mouse model. Different studies, on several pathologies of bacterial origin, mentioned the injection of 105 to 107 CFU.ml-1 (colony forming units) per mouse by intravenous route.
We chose to realize this experiment on 3 murine model: immunodepressed, normal, and cancerous.

3modelmurinEn.png

According to several studies, it seems that mycobacteria has a specific affinity for fibronectins, surexpressed at the surface of tumor cells. Mycobacterial tropism for tumor area has not been yet demonstrated, the cancerous murine model allows us to test this hypothesis.


Back to top

Experimental protocol details

  • Day -7: Inoculation of 104 LBS cells (fibroblastic cancer cells) subcutaneously on 2 black 6 mice.
  • Day 0: Inoculation of 106 CFU.ml-1* of tissue vectors, M.avium, by IV route (intravenous) injected in the tail of the 3 mouse models: immunodepressed, cancer, and normal (2 mice per model).
The concentration of injected tissue vectors was determined by measuring the optical density. The optical density of 106 bacteria is not detectable in a spectrophotometer. We therefore measured the cell suspension absorbance of 108 bacteria. Once diluted by 100, we obtained the desired concentration is: 106 bacteria.
  • Day 7: Mice sacrifice, organs extraction and cell suspension obtention, from the lungs, liver, spleen.

The cell suspension obtained is then analyzed by flow cytometry, to verify the size and granularity of cells. These 2 characteristics are totally different between eukaryotic cells comprising murine organs, and the vector tissue M.avium of prokaryotic origin.
We can thus verify and quantify the presence of the vector tissue.


Back to top

Results

A lung sample of each murine models, has been analysed by flow cytometry, to determine and quantify our tissue vector presence, M.avium in the lungs. This experiment could not be repeated more than once, we can we can only be reserved against thèse results. Nevertheless, various publications have already demonstrated the Mycobacterium avium implantation in the lungs, thus proving the credibility and feasibility of this study.

Temoincyto.png

D’après les résultats ci-dessus, nous avons déterminé la signature d’un échantillon de Mycobacterium avium en cytométrie en flux (en rouge zone R1). L’image de gauche correspond au bruit de fond ou signaux parasites du cytomètre. Il aurait été cependant très intéressant de réaliser un 3e témoin, avec l’acquisition d’un échantillon de poumons de souris non infecté par M. avium.

Echancyto1En.png

In the above samples, it is difficult to find specifically the signature of the « mycobacterium » sample. It is also very difficult to discern any difference between the 2 mouse model, Nod Scid and Black 6.

float

The opposite samples, does not allow us to determine a possible influence of the subcutaneous tumor on the mycobacterial tropism, or even to differentiate the M. avium tropism in this model, from others models.


Back to top

Discussion

This experiment achieved only a single time, failed to meet our goals, to identify and quantify the M. avium tropisms. However, lack of time is another factor to consider. Indeed, this analysis by flow cytometry was performed one week after the injection of M. avium in mice. After reading various publications, it is interesting to note that the significant data of M. avium implantation in the lungs, are obtained after many weeks. Therefore, it explains our difficulty to quantify by flow cytometry, the presence of the vector tissue after one week.

float

The above figure is extracted from the publication « Thymus as a target for mycobacterial infections ». A similar protocol was performed with injection of 10 ^ 6 CFU / ml M. <i> avium administered intravenously. . It is described in this figure that the lungs are infected from the first day of infection, but in very small amount (just over 10 ^ 1, then it is more prolonged with the rapid spread (10 ^ 1 to 10 ^ 6 CFU / organ in less than 5 weeks). This proves, therefore, that the lungs are colonized by M. avium .


Back to top

Conclusion

Although our study does not prove significantly the presence of M. avium in the lung, it has been proven many times that this type of bacteria colonizes the lung. This organ is a one of the natural tropisms of M. avium in mice and humans.
We can use the DVS on lung cancer, because we are confident that the vector tissue can target the organism and release the cell vector.


Back to top