» Articles » PMID: 9826671

Quantitative Insight into Proliferation and Differentiation of Oligodendrocyte Type 2 Astrocyte Progenitor Cells in Vitro

Overview
Specialty Science
Date 1998 Nov 25
PMID 9826671
Citations 15
Authors
Affiliations
Soon will be listed here.
Abstract

As part of our attempts at understanding fundamental principles that underlie the generation of nondividing terminally differentiated progeny from dividing precursor cells, we have developed approaches to a quantitative analysis of proliferation and differentiation of oligodendrocyte type 2 astrocyte (O-2A) progenitor cells at the clonal level. Owing to extensive previous studies of clonal differentiation in this lineage, O-2A progenitor cells represent an excellent system for such an analysis. Previous studies have resulted in two competing hypotheses; one of them suggests that progenitor cell differentiation is symmetric, the other hypothesis introduces an asymmetric process of differentiation. We propose a general model that incorporates both such extreme hypotheses as special cases. Our analysis of experimental data has shown, however, that neither of these extreme cases completely explains the observed kinetics of O-2A progenitor cell proliferation and oligodendrocyte generation in vitro. Instead, our results indicate that O-2A progenitor cells become competent for differentiation after they complete a certain number of critical mitotic cycles that represent a period of symmetric development. This number varies from clone to clone and may be thought of as a random variable; its probability distribution was estimated from experimental data. Those O-2A cells that have undergone the critical divisions then may differentiate into an oligodendrocyte in each of the subsequent mitotic cycles with a certain probability, thereby exhibiting the asymmetric type of differentiation.

Citing Articles

Regulation of DM-20 mRNA expression and intracellular translocation of glutathione-S-transferase pi isoform during oligodendrocyte differentiation in the adult rat spinal cord.

Kitada M, Takeda K, Dezawa M Histochem Cell Biol. 2016; 146(1):45-57.

PMID: 26921198 DOI: 10.1007/s00418-016-1421-z.


ASYMMETRIC CELL DIVISION: IMPLICATIONS FOR GLIOMA DEVELOPMENT AND TREATMENT.

Lewis K, Petritsch C Transl Neurosci. 2014; 4(4):484-503.

PMID: 25530875 PMC: 4269374. DOI: 10.2478/s13380-013-0148-8.


Limiting Distributions for Multitype Branching Processes.

Yakovlev A, Yanev N Stoch Anal Appl. 2013; 28(6):1040-1060.

PMID: 24031155 PMC: 3768166. DOI: 10.1080/07362994.2010.515486.


Modeling Cell Kinetics using Branching Processes with Non-Homogeneous Poisson Immigration.

Hyrien O, Yanev N C R Acad Bulg Sci. 2013; 63(10):1405-1414.

PMID: 23729973 PMC: 3666344.


Two-Type Age-Dependent Branching Processes with Inhomogeneous Immigration as Models of Renewing Cell Populations.

Hyrien O, Yanev N Pliska. 2013; 20:81-108.

PMID: 23729950 PMC: 3666601.


References
1.
Bogler O, Wren D, Barnett S, Land H, Noble M . Cooperation between two growth factors promotes extended self-renewal and inhibits differentiation of oligodendrocyte-type-2 astrocyte (O-2A) progenitor cells. Proc Natl Acad Sci U S A. 1990; 87(16):6368-72. PMC: 54535. DOI: 10.1073/pnas.87.16.6368. View

2.
Gao F, Raff M . Cell size control and a cell-intrinsic maturation program in proliferating oligodendrocyte precursor cells. J Cell Biol. 1997; 138(6):1367-77. PMC: 2132550. DOI: 10.1083/jcb.138.6.1367. View

3.
von Collani E, Tsodikov A, Yakovlev A, Mayer-Proschel M, Noble M . A random walk model of oligodendrocyte generation in vitro and associated estimation problems. Math Biosci. 1999; 159(2):189-204. DOI: 10.1016/s0025-5564(99)00017-6. View

4.
Barnett S, Crouch D . The effect of oncogenes on the growth and differentiation of oligodendrocyte type 2 astrocyte progenitor cells. Cell Growth Differ. 1995; 6(1):69-80. View

5.
Yakovlev A, Mayer-Proschel M, Noble M . A stochastic model of brain cell differentiation in tissue culture. J Math Biol. 1998; 37(1):49-60. DOI: 10.1007/s002850050119. View