Front Matter

(Rick Simeone) #1
(a)

(b)

(c)


1 A B C D E
234 5 6 7 8 9

Day 0Day 2Day 4Day 6Day 8

NBC cell line containing
unknown numbers of
progenitor cells

Growth pattern of a single-cell clone from a single cell into a larger cluster of cells from day 0 to day 8

Each of the single-cell clones
were expanded and the
clones were characterized
with monoclonal antibodies
to brain specific antigens

Single cells were seeded into
each well of 96-well plate and
single cells were allowed to grow
until each single-cell clone reach
confluency. The single-cell
clones were then transferred into
larger flask and allowed to grow
until 90% confluency Screened with monoclonal
antibodies

Figure 7.1 (a) Various kinds of neuronal progenitor cells. Each color represents a unique
progenitor cell in weeks 4–8 fetal brain, destined to become one of the compartments of an
adult brain. Elimination of one of the cell types may result in complete or partial absence of
a future compartment of a brain. Depletion of a single cell at an early developmental stage
can result in a cognitive deficit. (b) The process of single‐cell cloning. The neuroblastoma
cell line is cultured in a specialized cell culture flask, and the cells are then trypsinized to
separate each of the cells (each representing a unique fetal brain progenitor cell).
The individual cells are seeded into a 96‐well plate until they grow in a cellular cluster.
Each of the clusters is then transferred into a new culture flask. Each clone is then
characterized by immunostaining (c). (c) The visual microscopic presentation of a single-cell
clone that grows into a large cluster-from day 0 to day 8.

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