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- Open Access
In silico investigation of ADAM12 effect on TGF-β receptors trafficking
© Gruel et al; licensee BioMed Central Ltd. 2009
- Received: 11 May 2009
- Accepted: 24 September 2009
- Published: 24 September 2009
The transforming growth factor beta is known to have pleiotropic effects, including differentiation, proliferation and apoptosis. However the underlying mechanisms remain poorly understood. The regulation and effect of TGF-β signaling is complex and highly depends on specific protein context. In liver, we have recently showed that the disintegrin and metalloproteinase ADAM12 interacts with TGF-β receptors and modulates their trafficking among membranes, a crucial point in TGF-β signaling and development of fibrosis. The present study aims to better understand how ADAM12 impacts on TGF-β receptors trafficking and TGF-β signaling.
We extracted qualitative biological observations from experimental data and defined a family of models producing a behavior compatible with the presence of ADAM12. We computationally explored the properties of this family of models which allowed us to make novel predictions. We predict that ADAM12 increases TGF-β receptors internalization rate between the cell surface and the endosomal membrane. It also appears that ADAM12 modifies TGF-β signaling shape favoring a permanent response by removing the transient component observed under physiological conditions.
In this work, confronting differential models with qualitative biological observations, we obtained predictions giving new insights into the role of ADAM12 in TGF-β signaling and hepatic fibrosis process.
- Liver Fibrosis
- Kinetic Coefficient
- Differential Model
- Chronic Liver Injury
- Transient Component
During chronic liver injury, the sustained wound healing response leads to fibrosis and cirrhosis. Among the molecular components involved in fibrogenesis, the transforming growth factor, TGF-β is the most potent profibrotic cytokine. Indeed, several authors have shown that alteration of TGF-β dependent signaling pathway is associated with liver fibrosis [1, 2]. In this system, the first cellular control point is at the membrane. TGF-β transmits its signal through a heteromeric complex of two types of transmembrane receptors, Tβ RI and Tβ RII. TGF-β binding to Tβ RII induces recruitment and phosphorylation of Tβ RI, which activates R-Smad intracellular signaling . At the membrane, an important feature of TGF-β signaling is the continuous internalization of receptors and ligand-receptor complexes through two endocytosis pathways: the clathrin-coated pit endocytosis, mediating R-Smad signaling cascade, and the caveolin mediated endocytosis, leading to degradation of receptors through the proteasome pathway [4, 5].
We have recently demonstrated that ADAM12, a member of the disintegrin and metalloproteinase family associated with liver fibrogenesis [6, 7], facilitates TGF-β signaling at the membrane . ADAM12 interacts with Tβ RII and enhances TGF-β activity by modulating TGF-β receptor trafficking. In order to understand how ADAM12 expression might affect TGF-β signaling activity, we investigated mathematical models for ADAM12-dependent TGF-β signaling pathways. Based on models describing physiological TGF-β receptor trafficking and using a fitting procedure based on biological qualitative observations, we computed a family of models mimicking the pathological trafficking involving ADAM12. Their analysis allowed us to predict new effects of ADAM12 on TGF-β signaling.
Mathematical models of TGF-β receptor trafficking
List of abbreviations
Receptors production rate
Internalization rate towards endosome
Recycling rate from endosome
Internalization rate towards caveosome
Recycling rate from caveosome
Constitutive degradation rate
Ligand induced degradation rate
LRC formation rate
Receptor complexes in the cell membrane
Receptor complexes in the endosome
Receptor complexes in the caveosome
LRCs at the cell surface membrane
LRCs in the endosome
LRCs in the caveosome
Constitutive to Induced degradation Ratio
Physiological values of kinetic coefficients in V-model and Z-model
p R - Receptors production rate
k ie - Internalization rate towards endosome
k re - Recycling rate from endosome
k ic - Internalization rate towards caveosome
k rc - Recycling rate from caveosome
k cd - Constitutive degradation rate
k lid - Ligand induced degradation rate
k a - LRC formation rate
Receptors and ligand
Tβ RI and Tβ RII are considered as a single receptor complex (named R) since the two receptors have been reported to traffic complexed together. At the cell surface membrane and upon TGF-β stimulation this complex can form a ligand-receptor complex (LRC). We note that homomeric Tβ RII complexes have been reported to bind TGF-β, however they have not shown any direct role in signaling  and are thus eluded.
Receptors and LRCs can be present at the cell surface membrane and in internal membranes. There is a constant trafficking between those compartments which is unaffected by the presence of TGF-β. Internalization and recycling routes exist between the cell surface membrane and two inner compartments, the endosome (k ie , k re ) and the caveosome (k ic , k rc ).
Production and degradation of receptors
Constitutive production of receptors toward the cell surface membrane (p R ) is balanced by constitutive degradation (k cd ), equally affecting receptors and LRCs. LRCs present in the caveosome undergo a ligand-induced degradation (k lid ). Constitutive degradation happens either at the cell surface (V-model) or in the endosome (Z-model).
Signal transmission to downstream components of the TGF-β pathway is mediated through LRC association with R-Smads in the endosomal compartment. According to , TGF-β signaling is assumed to be proportional to the amount of LRCs internalized in the endosome.
Qualitative fitting procedure
Our biological data  suggest that, whether ADAM12 is present or not, receptors keep trafficking among the same compartments and are subject to the same degradation processes. We thus made the hypothesis that ADAM12 does not modify the structure of the receptor trafficking, but rather modulates the involved kinetic coefficients.
Biological observations and mathematical translation
an increase of R-Smads phosphorylation and an increase of the transcription of some SMAD regulated genes is observed upon addition of ADAM12 
at stable state, with TGF-β, the amount of LRCs present in the endosome is increased by at least a factor 2
cells transfected with Tβ RII and increasing amounts of ADAM12 proved that the more ADAM12 there was, the higher the steady state level of Tβ RII was 
at stable state, without TGF-β, the total amount of receptors present in the system is increased by at least a factor 2
immunofluorescence studies showed that ADAM12 modifies the ratio of the Tβ RII present at the cell surface membrane out of those internalized, favoring the intracellular compartments 
at stable state, without TGF-β, the ratio of internalized receptors out of those present in the membrane is increased by at least a factor 2
ADAM12 expression decreases the amount of SMAD7 complexed with ligand-receptor complexes, and thus their ubiquitination 
at stable state, with TGF-β, the ligand induced degradation flow is decreased by at least a factor 2
overexpression studies with ADAM12 and gene reporter assay showed that ADAM12 does not maintain transcriptional activity after TGF-β removal (unpublished data)
after stabilization with TGF-β, and removal of TGF-β, the amount of LRCs present in the endosome becomes negligible within the first 200 minutes
ADAM12 increases internalization from cell surface to endosome
The algorithm allows all coefficient multipliers to range from 0.1 to 10. While most coefficients present this dispersion, 3 are more tightly constrained. They are k ie , k re and k cd .
To take ADAM12 effect into account, the recycling rate from endosome to cell surface (k re ) is allowed to decrease (up to 0.69 times the physiological coefficient for V-model, 0.66 for Z-model) or to increase (up to 3.08 for V-model, 3.56 for Z-model). The constitutive degradation (k cd ) has to decrease for Z-model solutions (maximal multiplier: 0.33). The only coefficient that follows the same trend, in every solution, is the internalization towards the endosome (k ie ), it has to increase by at least a factor 2.14 or 2.05 for V-model or Z-model architectures, respectively. Thus, the only hard prediction that can be drawn from these allowed kinetic coefficient variations, is that ADAM12 has to increase k ie to accord with the defined constraints. However this increase remains insufficient to explain the effect of ADAM12, as no model fits with this kinetic coefficient variation only.
Another interesting observation is that the amount of modified kinetic parameters, compared to physiological models, greatly varies from one ADAM12 model to another. Following Occam's razor, we considered the models displaying the fewer modifications. These are models following V-model architecture. They are characterized by an increased rate of receptor internalization towards the endosome and a decreased rate of internalization towards the caveosome. These modifications could be explained by a single effect of ADAM12, a redistribution of TGF-β receptors at the cell surface membrane, closer to clathrin pits and farther from caveolae.
ADAM12 induces a permanent response to TGF-β
The constitutive to induced degradation ratio (CIR) characterizes the response type to TGF-β. Upon TGF-β stimulation, a low CIR implies a transient response followed by an important decrease of the signal. In high CIR value systems, the decreasing phase tends to disappear and the signaling output is sustained at high values.
We computed a CIRlike value, which generalizes the CIR properties, to characterize the reponse type of TGF-β under the potential effects of ADAM12. It was computed at the stable state of the models.
ADAM12 is up-regulated during chronic liver injury [6, 7] and modulates TGF-β activity , thereby contributing to TGF-β dependent liver fibrosis. In this work, we fitted differential models describing the well documented system of TGF-β receptor trafficking to take into account new observations on the perturbations occurring in presence of ADAM12. This led us to propose a set of possible models describing pathological situation. Studying the differences between the physiological models and the new ones, provides information about the effect of ADAM12 that could not have been drawn using only experimental observations.
Based on previous studies [9, 10], we first designed differential models handling TGF-β receptors trafficking among membranes (V-model and Z-model). The structural difference between these models is the constitutive degradation localized at the cell surface membrane in V-model and in the endosome in Z-model. Constitutive degradation is assumed to occur at the end of the endosomal maturation process, when internalized receptors go through early endosome, late endosome and are then degraded in the lysosome. The hypothesis by Vilar et al.  implies that a sorting mechanism occurs at the cell surface membrane, separating the elements that will undergo degradation from those that will be recycled back to the cell surface. As the endosomal dynamics are still far from being fully understood, this hypothesis cannot be dismissed, and we studied the two propositions.
Using a heuristic search, driven by a cost function derived from qualitative biological data, we defined the set of possible models handling ADAM12. Those models suggest that the presence of ADAM12 increases the internalization rate of TGF-β receptors between the cell surface membrane and the endosome. An interesting aspect is that ADAM12 might not only affect TGF-β signaling strength but also its shape. This comes from the modification of the ratio between constitutive degradation and ligand induced degradation (CIRlike), favoring the first one. In presence of ADAM12, the predicted signaling response to TGF-β seems like a step increase, maintaining a permanent and high level response replacing the transient component of the physiological response. Interestingly, other signaling pathways were shown to produce different responses depending on the shape of the input signal. For instance, a transient activation of the MAPK cascade in EGF pathaway leads to cell proliferation while a permanent activation leads to cell differentiation . In our case, ADAM12, which according to our predictions modifies TGF-β signaling, could be partly responsible for the changes observed in TGF-β signaling during liver fibrosis.
Finally, although many models for the possible effect of ADAM12 differ from the physiological models by all the kinetic parameters, it is difficult to imagine that ADAM12 could have such a wide range of action, i.e. changing every parameter. In fact, some models are a lot more parsimonious. For instance, a group of them only shows an increased rate of internalization towards the endosome and a decreased rate of internalization towards the caveosome. Under such assumption, the effect of ADAM12 could be a redistribution of TGF-β receptors in the cell surface membrane closer to clathrine pits and farther from caveolae. Interestingly, Interleukin-6 (IL-6), an important regulator of inflammation, has been suggested to similarly decrease the partitioning of TGF-β receptors to the raft-caveolin membrane fractions while enhancing TGF-β signaling activity .
Taken together, our data give new insights into the role of ADAM12 in TGF-β signaling. Our models predict that its impact might contribute to the sustained TGF-β activity that triggers liver fibrosis.
This work was supported by the Institut National de la Santé et de la Recherche Médicale, the Association pour la Recherche contre le Cancer, the Ligue Contre le Cancer and the Region Bretagne (PRIR n° 3193).
- Bissell DM: Chronic liver injury, TGF-beta, and cancer. Exp Mol Med. 2001, 33: 179-190.View ArticlePubMedGoogle Scholar
- Dooley S, Delvoux B, Lahme B, Mangasser-Stephan K, Gressner AM: Modulation of transforming growth factor beta response and signaling during transdifferentiation of rat hepatic stellate cells to myofibroblasts. Hepatology. 2000, 31: 1094-1106. 10.1053/he.2000.6126.View ArticlePubMedGoogle Scholar
- Massagué J: How cells read TGF-beta signals. Nat Rev Mol Cell Biol. 2000, 1: 169-178. 10.1038/35043051.View ArticlePubMedGoogle Scholar
- Hayes S, Chawla A, Corvera S: TGF beta receptor internalization into EEA1-enriched early endosomes: role in signaling to Smad2. J Cell Biol. 2002, 158: 1239-1249. 10.1083/jcb.200204088.PubMed CentralView ArticlePubMedGoogle Scholar
- Di Guglielmo GM, Le Roy C, Goodfellow AF, Wrana JL: Distinct endocytic pathways regulate TGF-beta receptor signalling and turnover. Nat Cell Biol. 2003, 5: 410-421. 10.1038/ncb975.View ArticlePubMedGoogle Scholar
- Le Pabic H, Bonnier D, Wewer UM, Coutand A, Musso O, Baffet G, Clément B, Théret N: ADAM12 in human liver cancers: TGF-beta-regulated expression in stellate cells is associated with matrix remodeling. Hepatology. 2003, 37: 1056-1066. 10.1053/jhep.2003.50205.View ArticlePubMedGoogle Scholar
- Le Pabic H, L'Helgoualc'h A, Coutant A, Wewer UM, Baffet G, Clément B, Théret N: Involvement of the serine/threonine p70S6 kinase in TGF-betal-induced ADAM12 expression in cultured human hepatic stellate cells. J Hepatol. 2005, 43: 1038-1044. 10.1016/j.jhep.2005.05.025.View ArticlePubMedGoogle Scholar
- Atfi A, Dumont E, Colland F, Bonnier D, L'helgoualc'h A, Prunier C, Ferrand N, Clément B, Wewer UM, Théret N: The disintegrin and metalloproteinase ADAM12 contributes to TGF-beta signaling through interaction with the type II receptor. J Cell Biol. 2007, 178: 201-208. 10.1083/jcb.200612046.PubMed CentralView ArticlePubMedGoogle Scholar
- Vilar JM, Jansen R, Sander C: Signal processing in the TGF-beta superfamily ligand-receptor network. PLoS Comput Biol. 2006, 2: e3-10.1371/journal.pcbi.0020003.PubMed CentralView ArticlePubMedGoogle Scholar
- Zi Z, Klipp E: Constraint-based modeling and kinetic analysis of the Smad dependent TGF-beta signaling pathway. PLoS ONE. 2007, 2: e936-10.1371/journal.pone.0000936.PubMed CentralView ArticlePubMedGoogle Scholar
- Doré JJ, Edens M, Garamszegi N, Leof EB: Heteromeric and homomeric transforming growth factor-beta receptors show distinct signaling and endocytic responses in epithelial cells. J Biol Chem. 1998, 273: 31770-31777. 10.1074/jbc.273.48.31770.View ArticlePubMedGoogle Scholar
- Mitchell H, Choudhury A, Pagano RE, Leof EB: Ligand-dependent and -independent transforming growth factor-beta receptor recycling regulated by clathrin-mediated endocytosis and Rabll. Mol Biol Cell. 2004, 15: 4166-4178. 10.1091/mbc.E04-03-0245.PubMed CentralView ArticlePubMedGoogle Scholar
- Inman GJ, Nicolás FJ, Hill CS: Nucleocytoplasmic shuttling of Smads 2, 3, and 4 permits sensing of TGF-beta receptor activity. Mol Cell. 2002, 10: 283-294. 10.1016/S1097-2765(02)00585-3.View ArticlePubMedGoogle Scholar
- Vaudry D, Stork PJ, Lazarovici P, Eiden LE: Signaling pathways for PC12 cell differentiation: making the right connections. Science. 2002, 296: 1648-1649. 10.1126/science.1071552.View ArticlePubMedGoogle Scholar
- Zhang XL, Topley N, Ito T, Phillips A: Interleukin-6 regulation of transforming growth factor (TGF)-beta receptor compartmentalization and turnover enhances TGF-betal signaling. J Biol Chem. 2005, 280: 12239-12245. 10.1074/jbc.M413284200.View ArticlePubMedGoogle Scholar
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