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The basic thesis for this study was that the telencephalon is
needed to make decisions in new situations. Subsidary hypotheses
were that the telencephalon consists of: (a) a sensorimotor system
which generates motor activity from sensory input and (b) a
selection system which makes choices from possible motor programs.
It was postulated that the selection system should fulfil the
following requirements: be accessible for past and present events,
have the capacity to process this information in a nondetermined
way with a possibility for ordering, and have access to
motor-affecting systems (the sensorimotor system). The ability of
the selection system to correlate information in a nonpredetermined
way was considered most important. In short: The selection system
should be able to associate any information in any combination, and
have the capability for internal control of neuronal activity and
external selection of motor programs (see Fig. IA. ) Xenopus laevis
was chosen as a subject, since it has a relatively simple tel
encephalon, with characteristics that it shares with "primitive"
species of different vertebrate classes, and because it is easy to
maintain as a laboratory animal. The main method used was the
determination of connections with HRP. The pallium was in the focus
of attention, since it was considered to be the core of the
selection system. Immunohistochemistry was used as an additional
parameter to compare Xenopus laevis forebrain with those of other
vertebrates.
At the end of the nineteenth century, controversy arose as to
precisely when the first glial cells originate during development
of the central nervous system, and to date, the issue has not been
satisfactorily resolved. His (1889, 1890) noted that, even in the
earliest developmental stages of the germinallayer, there appeared
to be two distinct cell types. The cells which he called
Spongioblasten were thought to be glial precursors from which all
mature glial cells derive; Keimzellen, in contrast, were regarded
as forming 1 neurons. His was working on the assumption that the
very first preneurons migrate into a preexisting framework of glial
eelIs. In contrast to this view, Schaper (1897) regarded both
Keimzellen and Spongioblasten as belonging to a common population
of proliferating and pluripotent stem cells which begin
differentiation into glial and neuronal cells at late developmental
stages. It is this latter view which is the basis of the most
recent studies on the subject (e. g. , Caley and Maxwell1968a,
1968b; DeVitry et al. 1980). The concept of one common stem cell
seemed to be supported both by experiments using 3H-thymidine
autoradiography (Fujita 1963, 1965b, 1966; Sauer and Walker 1959;
Sidman et al. 1959) and by ultrastructural studies (Fu- jita 1966;
Hinds and Ruffet 1971; Wechseler and Meller 1967) indicating that
structural differences, which His presumably used to define his two
cell types, could be related to different stages of the mitotic
cycle.
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