Paris/Cell auto 2
From 2007.igem.org
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<embed style="width:350px; height:300px;" id="VideoPlayback" type="application/x-shockwave-flash" src="http://video.google.com/googleplayer.swf?docid=2422231061053866723&hl=en=en =en" flashvars=""> </embed></html></center> | <embed style="width:350px; height:300px;" id="VideoPlayback" type="application/x-shockwave-flash" src="http://video.google.com/googleplayer.swf?docid=2422231061053866723&hl=en=en =en" flashvars=""> </embed></html></center> | ||
- | *The first | + | *The first video show a first comportment |
- | : | + | :Red : BactG |
- | *The second picture show the | + | :Green : BactS |
+ | :dark<->light Bact : low<->high DAP | ||
+ | :The number of bacteria (G or S) increase with the time | ||
+ | *The second picture show the differentiation | ||
:Red BactG | :Red BactG | ||
:Green BactS | :Green BactS |
Revision as of 13:13, 22 October 2007
Contents |
Spacial simulation
We try with this work to characterize the diffusion of the DAP and the effect on the cells. We have a growing culture with germinal cells and somatic cells.
We want to see if we can have different kinds of evolution for our cells
We make some hypothesis:
We work with a evolving population ( death for BactS and division BactG).
- Case 1 : The differentiation is DAP dependent, it's append when the cell as enough DAP to evolve but not enough to divide.
- Case 2 : The differentiation has a constant rate, it will be the same rate for each division cycle
The DAP is made in bacteria S, the production rate is the difference between the total production and self consummation
We consider a global variable DAP (no internal/external DAP)
The DAP is consumed in bacteria G
All the cells grow
We have 3 entities in our model
Bact it has a concentration internal of DAP and a radius. It's a cell in our automaton
BactS is a Bact which produce DAP and can grow
BactG is a Bact which consume DAP and can divide or differentiate
Case 1
We produce this set of rules
Mechanic forces
- We create a spring between the center of each Bact, then we compute the forces related to this spring and we update the position of the cells (adding noise to it)
For bactS
- if random < Probability of death then
- BactS=null
- BactS=null
- else
- if random < probability to grow & size < max cell size then
- BactS=BactS+{new size=size+delta}
- else
- nothing
- nothing
- if random < probability to grow & size < max cell size then
- Produce DAP
For BactG
- DAP'=DAP - self consumed DAP - diffused DAP
- if enough DAP then
- if random< probability of differentiation then
- BactG=BactS
- else
- BactG= BactG+{DAP'}
- if random< probability of differentiation then
- else
- if size > max size then
- if probability to divide > random & DAP'> minimal needed to divide then
- BactG = 2 BactG with minimal size
- else BactG= BactG +{DAP=DAP'}
- if probability to divide > random & DAP'> minimal needed to divide then
- else
- if random < probability to grow then
- BactG = BactG + {new size= size + delta}
- else
- nothing
- if random < probability to grow then
- if size > max size then
Initial state
4 BactS and a BactG in the middle
Parameters
We have 8 parameters and we can had noise for each of them.
Mechanic
- DT time step
- K constant of the spring
- Mu variation of position
- R0_Gm minimal size of a BactG (after division)
- R0_G maximal size of a BactG (before division)
- R0_S maximal size of BactS
In Bact
- Diff diffusion constant
In BactS:
- Diffp probability of differentiation
- DEPOT production of DAP
- DeathSP probability of death
- CroitS probability of growth
In BactG:
- CONS Dap consumed
- DivG probability of division
- CroitG probability of growth
Output
The output is two videos showing the evolution of the organism
- The first video show a first comportment
- Red : BactG
- Green : BactS
- dark<->light Bact : low<->high DAP
- The number of bacteria (G or S) increase with the time
- The second picture show the differentiation
- Red BactG
- Green BactS
- The differentiation follow the wave front
After playing with the parameters, we can deduct 2 important things:
- The inhibition most be strong and effective (we play with the minimal and maximal value of DAP for differentiation)
- if it isn't the case the system collapse all the bactG stay BactG if the inhibition is too strong or switch to BactS if the inhibition is not enough strong.
- The production and diffusion of DAP will be a critical factor
- The DAP has to be produce then he will be exported, it will diffuse in the medium and will be imported
- There is no proof of a special systme to import or export DAP, so for each step there is a large amount of DAP lost.