GAP-43 Immunoreactivity in the brain of the developing and adult wallaby (Macropus eugenii)

Anatomy and Embryology - Tập 206 - Trang 97-118 - 2002
Maria Hassiotis1, Ken W. Ashwell1, Lauren R. Marotte2, Sabine Lensing-Höhn3, Jürgen K. Mai3
1Department of Anatomy, The University of NSW, 2052 Sydney, NSW, Australia,
2Developmental Neurobiology and Endocrinology Group, Research School of Biological Sciences, Australian National University, 2601 Canberra, Australia,
3Abteilung für Neuroanatomie, Heinrich Heine Universität, Düsseldorf 40001, Germany,

Tóm tắt

We have examined the distribution of immunoreactivity for GAP-43 in the developing and adult brain of a diprotodontid metatherian, the tammar wallaby (Macropus eugenii). The distribution of GAP-43 immunoreactivity in the neonatal wallaby brain was strikingly heterogeneous, in contrast to that reported for the newborn polyprotodontid opossum. Immunoreactivity for GAP-43 in the developing wallaby brain showed a caudal-to-rostral spatiotemporal gradient, with the brainstem well in advance of the telencephalon throughout the first 100 days of postnatal life. In many regions examined, GAP-43 immunoreactivity passed through the following phases: 1. intense immunoreactivity in developing fiber tracts and occasional somata; 2. diffuse homogeneous immunoreactivity; 3. selective loss of immunoreactivity in particular nuclei or cortical regions. In the isocortex, selective loss of GAP-43 immunoreactivity in the somatosensory and visual cortex (at postnatal day 115) coincided with the maturation of the laminar distribution of terminal thalamocortical axonal fields. Within adult cortical regions, GAP-43 immunoreactivity was highest in layer I of all regions, lower layers (V and VI) of primary somatosensory and visual cortices, layers II/III of motor and cingulate cortex, and layer IV of entorhinal cortex. Our findings suggest that, while patterning of GAP-43 immunoreactivity in the mature brain is similar across meta- and eutheria, there may be early developmental differences in the distribution of GAP-43 immunoreactivity between poly- and diprotodontid metatheria.