- Author:
- Catherine Lloyd <c.lloyd@auckland.ac.nz>
- Date:
- 2009-12-09 14:56:07+13:00
- Desc:
- Fixed cmeta id's - they didn't match and the RDF wasn't rendereing properly.
- Permanent Source URI:
- https://models.cellml.org/workspace/halloy_bernard_loussouarn_goldbeter_2002/rawfile/3ca860198ba8e27cecfe770647fdcb77d46169b1/halloy_bernard_loussouarn_goldbeter_2002.cellml
<?xml version="1.0" encoding="utf-8"?>
<!--
This CellML file was generated on 7/12/2009 at 2:47:41 at p.m. using:
COR (0.9.31.1333)
Copyright 2002-2009 Dr Alan Garny
http://cor.physiol.ox.ac.uk/ - cor@physiol.ox.ac.uk
CellML 1.0 was used to generate this model
http://www.cellml.org/
-->
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<title>The Follicular Automaton Model for Hair Cycles</title>
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<firstname>Catherine</firstname>
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<title>Model Status</title>
<para>This CellMl model runs in PCEnv and to recreate the same steady state output of the original published model (as seen in in figure 5(d)). The units have been checked and they are consistent. The model also runs in COR, but due to the long time scale (in months as opposed to milliseconds), it cannot be used to recreate figure 5. The CellMl model represents the deterministic version of the follicular automaton modelc. Currently CellML cannot be used to describe stochastic variables.
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ABSTRACT: Human scalp hair consists of a set of about 10 to the 5 follicles which progress independently through developmental cycles. Each hair follicle successively goes through the anagen (A), catagen (C), telogen (T) and latency (L) phases that correspond, respectively, to growth, arrest and hair shedding before a new anagen phase is initiated. Long-term experimental observations in a group of ten male, alopecic and non-alopecic volunteers allowed determination of the characteristics of hair follicle cycles. On the basis of these observations, we previously proposed a follicular automaton model to simulate the dynamics of human hair cycles and the development of different patterns of alopecia [Halloy et al. (2000) Proc. Natl Acad. Sci. U.S.A.97, 8328-8333]. The automaton model is defined by a set of rules that govern the stochastic transitions of each follicle between the successive states A, T, L and the subsequent return to A. These transitions occur independently for each follicle, after time intervals given stochastically by a distribution characterized by a mean and a standard deviation. The follicular automaton model was shown to account both for the dynamical transitions observed in a single follicle, and for the behaviour of an ensemble of independently cycling follicles. Here, we extend these results and investigate additional properties of the model. We present a deterministic version of the follicular automaton. We show that numerical simulations of the stochastic version of the automaton yield steady-state level of follicles in the different phases which approach the levels predicted by the deterministic equations as the number of follicles progressively increases. Only the stochastic version can successfully reproduce the fluctuations of the fractions of follicles in each of the three phases, observed in small follicle populations. When the standard deviation is reduced or when the follicles become otherwise synchronized, e.g. by a periodic external signal inducing the transition of anagen follicles into telogen phase, large-amplitude oscillations occur in the fractions of follicles in the three phases. These oscillations are not observed in humans but are reminiscent of the phenomenon of moulting observed in a number of mammalian species. Copyright 2002 Elsevier Science Ltd.
</para>
<para>
The original paper reference is cited below:
</para>
<para>The Follicular Automaton Model: Effect of Stochasticity and of Synchronization of Hair Cycles, J. Halloy, B.A. Bernard, G. Loussouarn and A. Goldbeter, 2002,
<emphasis>Journal of Theoretical Biology</emphasis>
, 214, 469-479. <ulink url="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=PubMed&list_uids=11846603&dopt=Abstract">PubMed ID: 11846603</ulink>
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<caption>The above diagram represents the transition of a model hair follicle from anagen (A) to telogen (T) to latency (L) phase, successively. After phase T, the follicle may either die or miniaturise (transition to M; this usually occurs after a critical number of cycles), or complete a cycle by entering a new A phase.</caption>
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The model runs in the PCEnv simulator but gives a flat output.</rdf:value>
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<map_components component_1="L" component_2="reaction_constants"/>
<map_variables variable_1="mu_L" variable_2="mu_L"/>
<map_variables variable_1="mu_T" variable_2="mu_T"/>
<map_variables variable_1="mu_A" variable_2="mu_A"/>
<map_variables variable_1="epsilon" variable_2="epsilon"/>
</connection>
<connection xmlns="http://www.cellml.org/cellml/1.0#">
<map_components component_1="M" component_2="reaction_constants"/>
<map_variables variable_1="epsilon" variable_2="epsilon"/>
</connection>
</model>
