Spatial and temporal patterns of transneuronal labeling in CNS neurons after injection of pseudorabies virus into the sciatic nerve of adult rats

Citation
Es. Kim et al., Spatial and temporal patterns of transneuronal labeling in CNS neurons after injection of pseudorabies virus into the sciatic nerve of adult rats, BRAIN RES, 857(1-2), 2000, pp. 41-55
Citations number
53
Categorie Soggetti
Neurosciences & Behavoir
Journal title
BRAIN RESEARCH
ISSN journal
00068993 → ACNP
Volume
857
Issue
1-2
Year of publication
2000
Pages
41 - 55
Database
ISI
SICI code
0006-8993(20000228)857:1-2<41:SATPOT>2.0.ZU;2-9
Abstract
The distribution of labeled neurons in the brain and spinal cord was studie d after injecting the Bartha strain of pseudorabies virus (PRV) into the sc iatic nerve to provide a baseline for studying neural circuitry after spina l cord injury (SCI) and regeneration. Following a single injection of viral particles into the left sciatic nerve, PRV labeling was found in the spina l cord at 2 days post-injection (p.i.). Increasing complexity in viral labe ling from the spinal cord to supraspinal regions became apparent with incre asing survival time. In brain regions, several neuronal groups that regulat e sympathetic outflow, such as the rostroventrolateral medulla, the lateral paragigantocellular nuclei, and the A5 cells, were densely labeled. Howeve r, relatively sparse labeling was noticed in the lateral vestibular nuclei, the red nucleus and the motor cortex whose spinal projections regulate som atic motor function, although those areas were abundantly labeled with Fast blue (FB) in a double-labeling experiment in which FB was co-injected into the lumbar cord. The pattern of viral labeling became more complex beyond 5 days p.i, when increased numbers of cell groups were labeled with PRV but not FB. In addition, some infected neurons started to lyse, as evidenced b y a decrease in viral labeling at 7 days p.i. Thus, the 5th day post-viral injection would appear to be an appropriate survival time to obtain maximal labeling with acceptable specificity. We suggest that transneuronal labeli ng using PRV should be appropriate for studying multi-neural circuitry afte r SCI and regeneration. (C) 2000 Elsevier Science B.V. All rights reserved.