Differential distribution of immunoreactivity in the developing rat spinalcord revealed by the monoclonal antibody Py

Citation
Da. Houweling et al., Differential distribution of immunoreactivity in the developing rat spinalcord revealed by the monoclonal antibody Py, DEV BRAIN R, 116(1), 1999, pp. 87-96
Citations number
24
Categorie Soggetti
Neurosciences & Behavoir
Journal title
DEVELOPMENTAL BRAIN RESEARCH
ISSN journal
01653806 → ACNP
Volume
116
Issue
1
Year of publication
1999
Pages
87 - 96
Database
ISI
SICI code
0165-3806(19990805)116:1<87:DDOIIT>2.0.ZU;2-R
Abstract
Monoclonal antibody Py was developed as a useful tool for the identificatio n of large diameter neurons of the adult rat central nervous system [Woodha ms et al., J. Neurosci., 9 (1989) 2170-2181]. Here, we present a detailed l ight-microscopic study of the distribution of Py-immunoreactivity in the de veloping rat spinal cord. The first cells which demonstrated Py-immunoreact ivity were the motoneurons in layer IX of the gray matter at embryonic day 15. These cells, including their axons and dendrites, remained Py-immunorea ctive throughout subsequent developmental stages into adulthood and were th e most intensely stained cells in the adult rat spinal cord. Other cell pop ulations which became Py-immunoreactive during development were neurons in layers III-VIII, and large-to-medium diameter neurons of the dorsal root ga nglion (DRG). Transient Py-immunoreactivity was observed in the distal port ions of DRG axons as well as in the ascending fibers in the dorsal funiculu s. Py-immunoreactive fibers could be detected in the ventral most part of t he dorsal funiculus (corticospinal tract area), even at embryonic ages prio r to the arrival of corticospinal fibers. The localization and transient ex pression of the antigen recognized by the Py-antibody in developing rat spi nal cord strongly suggests an important role of this molecule in stabilizat ion and/or plasticity of the neuronal cytoskeleton. The results presented h ere form the foundation for the use of Py-immunocytochemistry to study well -defined cell populations under a range of experimental and pathological co nditions. (C) 1999 Elsevier Science B.V, All rights reserved.