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A Mathematical Model of Granule Cell Generation During Mouse Cerebellum Development.
Leffler, Shoshana R; Legué, Emilie; Aristizábal, Orlando; Joyner, Alexandra L; Peskin, Charles S; Turnbull, Daniel H.
Afiliação
  • Leffler SR; Skirball Institute of Biomolecular Medicine, New York University School of Medicine, 540 First Avenue, New York, NY, 10016, USA.
  • Legué E; Developmental Genetics Graduate Program, NYU School of Medicine, New York, NY, USA.
  • Aristizábal O; Developmental Biology Program, Sloan Kettering Institute, New York, NY, USA.
  • Joyner AL; Skirball Institute of Biomolecular Medicine, New York University School of Medicine, 540 First Avenue, New York, NY, 10016, USA.
  • Peskin CS; Developmental Biology Program, Sloan Kettering Institute, New York, NY, USA.
  • Turnbull DH; Courant Institute of Mathematical Sciences, New York University, 251 Mercer Street, New York, NY, 10012, USA. peskin@cims.nyu.edu.
Bull Math Biol ; 78(5): 859-78, 2016 05.
Article em En | MEDLINE | ID: mdl-27125657
ABSTRACT
Determining the cellular basis of brain growth is an important problem in developmental neurobiology. In the mammalian brain, the cerebellum is particularly amenable to studies of growth because it contains only a few cell types, including the granule cells, which are the most numerous neuronal subtype. Furthermore, in the mouse cerebellum granule cells are generated from granule cell precursors (gcps) in the external granule layer (EGL), from 1 day before birth until about 2 weeks of age. The complexity of the underlying cellular processes (multiple cell behaviors, three spatial dimensions, time-dependent changes) requires a quantitative framework to be fully understood. In this paper, a differential equation-based model is presented, which can be used to estimate temporal changes in granule cell numbers in the EGL. The model includes the proliferation of gcps and their differentiation into granule cells, as well as the process by which granule cells leave the EGL. Parameters describing these biological processes were derived from fitting the model to histological data. This mathematical model should be useful for understanding altered gcp and granule cell behaviors in mouse mutants with abnormal cerebellar development and cerebellar cancers.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Cerebelo / Neurônios Limite: Animals Idioma: En Revista: Bull Math Biol Ano de publicação: 2016 Tipo de documento: Article País de afiliação: Estados Unidos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Cerebelo / Neurônios Limite: Animals Idioma: En Revista: Bull Math Biol Ano de publicação: 2016 Tipo de documento: Article País de afiliação: Estados Unidos