Reusing and composing models of cell fate regulation of human bone precursor cells.
ASSAR, Rodrigo
Models and Algorithms for the Genome [ MAGNOME]
Center for Genome Regulation [Santiago] [CGR]
Voir plus >
Models and Algorithms for the Genome [ MAGNOME]
Center for Genome Regulation [Santiago] [CGR]
ASSAR, Rodrigo
Models and Algorithms for the Genome [ MAGNOME]
Center for Genome Regulation [Santiago] [CGR]
Models and Algorithms for the Genome [ MAGNOME]
Center for Genome Regulation [Santiago] [CGR]
INESTROSA, Nibaldo C
Centro de Regulación Celular y Patología Joaquín V. Luco, Departamento de Biología Celular y Molecular [CRCP]
Centro de Regulación Celular y Patología Joaquín V. Luco, Departamento de Biología Celular y Molecular [CRCP]
MONTECINO, Martín A
Center for Genome Regulation [Santiago] [CGR]
Centro de Investigaciones Biomédicas, Facultad de Ciencias Biológicas and Facultad de Medicina
< Réduire
Center for Genome Regulation [Santiago] [CGR]
Centro de Investigaciones Biomédicas, Facultad de Ciencias Biológicas and Facultad de Medicina
Langue
en
Article de revue
Ce document a été publié dans
BioSystems. 2012-04, vol. 108, n° 1-3, p. 63-72
Elsevier
Résumé en anglais
In order to treat osteoporosis and other bone mass disorders it is necessary to understand the regulatory processes that control the cell fate decisions responsible for going from bone precursor cells to bone tissue. Many ...Lire la suite >
In order to treat osteoporosis and other bone mass disorders it is necessary to understand the regulatory processes that control the cell fate decisions responsible for going from bone precursor cells to bone tissue. Many processes interact to regulate cell division, differentiation and apoptosis. There are models for these basic processes, but not for their interactions. In this work we use the theory of switched systems, reuse and composition of validated models to describe the cell fate decisions leading to bone and fat formation. We describe the differentiation of osteo-adipo progenitor cells by composing its model with differentiation stimuli. We use the activation of the Wnt pathway as stimulus to osteoblast lineage, including regulation of cell division and apoptosis. This model is our first step to simulate physiological responses in silico to treatments for bone mass disorders.< Réduire
Mots clés en anglais
Bone formation
Differentiation
Wnt pathway
Origine
Importé de halUnités de recherche