Cell lineage in the rat cerebral cortex: a study using retroviral-mediated gene transfer

Development ◽  
1988 ◽  
Vol 104 (3) ◽  
pp. 473-482 ◽  
Author(s):  
J. Price ◽  
L. Thurlow

We have used a retroviral vector that codes for the bacterial enzyme beta-galactosidase to study cell lineage in the rat cerebral cortex. This vector has been used to label progenitor cells in the cerebral cortices of rat embryos during the period of neurogenesis. When these embryos are allowed to develop to adulthood, the clones of cells derived from the marked progenitor cells can be identified histochemically. In this way, we can ask what are the lineage relationships between different neural cell types. From these studies, we conclude that there are two distinct types of progenitor cells in the developing cortex. One generates only grey matter astrocytes, whereas the second gives rise to neurones - both pyramidal and nonpyramidal - and to another class of cells that we have tentatively identified as glial cells of the white matter. We have also been able to address the question of how neurones are dispersed in the cortex during histogenesis. It had been previously hypothesized that clonally related neurones migrated radially to form columns in the mature cortex. However, we find that clones of neurones do not form radial columns; rather, they tend to occupy the same or neighbouring cortical laminae and to be spread over several hundreds of micrometers of cortex in the horizontal dimension. This spread occurs in both mediolateral and rostrocaudal directions.

Neuron ◽  
1995 ◽  
Vol 14 (6) ◽  
pp. 1181-1188 ◽  
Author(s):  
Brenda P Williams ◽  
Jack Price

PLoS ONE ◽  
2013 ◽  
Vol 8 (5) ◽  
pp. e63848 ◽  
Author(s):  
Christopher L. Cunningham ◽  
Verónica Martínez-Cerdeño ◽  
Stephen C. Noctor

2022 ◽  
Vol 15 ◽  
Author(s):  
Carla Belmonte-Mateos ◽  
Cristina Pujades

The central nervous system (CNS) exhibits an extraordinary diversity of neurons, with the right cell types and proportions at the appropriate sites. Thus, to produce brains with specific size and cell composition, the rates of proliferation and differentiation must be tightly coordinated and balanced during development. Early on, proliferation dominates; later on, the growth rate almost ceases as more cells differentiate and exit the cell cycle. Generation of cell diversity and morphogenesis takes place concomitantly. In the vertebrate brain, this results in dramatic changes in the position of progenitor cells and their neuronal derivatives, whereas in the spinal cord morphogenetic changes are not so important because the structure mainly grows by increasing its volume. Morphogenesis is under control of specific genetic programs that coordinately unfold over time; however, little is known about how they operate and impact in the pools of progenitor cells in the CNS. Thus, the spatiotemporal coordination of these processes is fundamental for generating functional neuronal networks. Some key aims in developmental neurobiology are to determine how cell diversity arises from pluripotent progenitor cells, and how the progenitor potential changes upon time. In this review, we will share our view on how the advance of new technologies provides novel data that challenge some of the current hypothesis. We will cover some of the latest studies on cell lineage tracing and clonal analyses addressing the role of distinct progenitor cell division modes in balancing the rate of proliferation and differentiation during brain morphogenesis. We will discuss different hypothesis proposed to explain how progenitor cell diversity is generated and how they challenged prevailing concepts and raised new questions.


Development ◽  
1991 ◽  
Vol 113 (Supplement_2) ◽  
pp. 23-28 ◽  
Author(s):  
Jack Price ◽  
Brenda Williams ◽  
Elizabeth Grove

We have studied cell lineage in the rat cerebral cortex using retroviral mediated gene transfer. By this method, a marker gene is inserted into dividing precursor cells such that their fate can be followed. We have applied this technique to two types of experiment. First, virus was used to label precursor cells of the cerebral cortex in situ during the period of neurogenesis. Second, cortical precursor cells were grown in dissociated cell culture, and virus was used to follow their development over the culture period. These experiments showed that the majority of precursor cells generate a single cell type – neurones, astrocytes, or oligodendrocytes. Moreover, this is true both in vivo and in dissociated cell culture. The only exception is a bipotential cell, which can generate both neurones and oligodendrocytes. These data suggest that the ventricular zone – the germinal layer of the embryonic cortex – is a mosaic of precursor cells of different restricted potentials. Although precursor cells are restricted in terms of the cell types they generate, they seem not to be restricted in either the cortical laminae or cytoarchitectonic areas to which they can contribute. Both neuronal and grey matter astrocyte precursors contribute cells to multiple layers of both infra- and supragranular laminae. Moreover, in the hippocampal formation, neuronal precursors can contribute cells to more than one hippocampal field.


2011 ◽  
Vol 23 (1) ◽  
pp. 1 ◽  
Author(s):  
Maziar Davanlou ◽  
Donald F Smith

The total numbers of neurons, glial cells, and endothelial cells in rat cerebral cortex were estimated using unbiased stereological counting techniques and systematic sampling. The reference volume chosen was the entire neocortex, most of the allocortex and parts of claustrum using the rhinal fissure as the macroscopical anatomical landmark. These regions are referred to collectively as syncortex. A method has been devised for reducing problems associated with the uncertainties that arise when distinguishing between various types of cells. At the light microscopic level, using the detailed criteria described in this article, the total numbers of neurons, glial cells, and endothelial cells, respectively, were estimated for the entire syncortex as the product of the estimate of the volume of the syncortex, made with point counting techniques, and the estimates of the numerical density for each group of cells, made with optical disectors. In a sample of three brains, the mean total number of cells (neurons, glial and endothelial) in the syncortex of the rat brain is 128 x 106. This number is made up of 47% neurons, 24% glial cells, 17% endothelial cells, and 11% uncertain cell types (probably mostly glial cells).


Development ◽  
1993 ◽  
Vol 117 (2) ◽  
pp. 553-561 ◽  
Author(s):  
E.A. Grove ◽  
B.P. Williams ◽  
D.Q. Li ◽  
M. Hajihosseini ◽  
A. Friedrich ◽  
...  

We have labelled precursor cells in the embryonic rat cerebral cortex using BAG, a retroviral vector that expresses beta-galactosidase. We had previously reported that labelled precursor cells generate clusters of labelled cells that could be classified into four types by their morphological appearance and anatomical distribution (Price and Thurlow, 1988). In this study, we have used immunohistochemistry and intracellular dye labelling to identify the cell types that make up these clusters. We discovered that clusters are almost always composed of a single cell type. In addition to clusters composed entirely of neurones, we found four different types of glial cell clusters. In the grey matter, glial clusters are composed either of protoplasmic astrocytes, or of cells that have an astrocyte morphology, but no glial filaments. In the white matter, clusters are composed of either fibrous astrocytes or oligodendocytes. Our results indicate that each of these different cortical cell types is generated from a separate population of precursor cells.


1991 ◽  
Vol 633 (1 Glial-Neurona) ◽  
pp. 56-63 ◽  
Author(s):  
JACK PRICE ◽  
BRENDA WILLIAMS ◽  
ROBERT MOORE ◽  
JOANNE READ ◽  
ELIZABETH GROVE

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