Unsuspected early neuronal loss in scrapie-infected mice revealed by morphometric analysis
- PMID: 8030955
- DOI: 10.1111/j.1749-6632.1994.tb38925.x
Unsuspected early neuronal loss in scrapie-infected mice revealed by morphometric analysis
Abstract
This study was undertaken to determine to what extent neuronal loss is a feature of scrapie pathology, using an experimental model in which infectivity and subsequent vacuolar lesions are well characterized but in which neuronal loss has not been previously identified. Intraocular infection with ME7 scrapie directs infection through the major projections of the optic nerve, which include the dorsal lateral geniculate nucleus (dLGN) on the contralateral side to the infected eye. Infectivity can be detected in the dLGN at 77 days post-infection and vacuolar lesions are first seen around halfway through the incubation period of 240 days. Morphometric assessment of neuron number in the dLGN was made on gallocyanin stained semi-serial sections from 5 infected and 5 normal brain-injected controls at 4 fifty-day intervals during the incubation period, and on clinically terminal mice. The number of neurons in the dLGN of the infected mice decreased steadily from around 20,000 at 50 days post-infection to under 2,000 in the terminal group. The loss was delayed in the ipsilateral dLGN, although terminal counts were the same for both sides. The onset of neuronal loss was coincident with initial vacuolar changes, and neuronal numbers were inversely proportional to the severity of vacuolation. It is concluded that scrapie infection causes a progressive neuronal loss that can be identified some 30-80 days after infectivity can be detected in the dLGN, long before the onset of clinical disease.
Similar articles
-
Early unsuspected neuron and axon terminal loss in scrapie-infected mice revealed by morphometry and immunocytochemistry.Neuropathol Appl Neurobiol. 1995 Feb;21(1):41-9. doi: 10.1111/j.1365-2990.1995.tb01027.x. Neuropathol Appl Neurobiol. 1995. PMID: 7770120
-
Electrophysiological properties of dorsal lateral geniculate neurons in brain slices from ME7 scrapie-infected mice.Exp Neurol. 1998 Jan;149(1):253-61. doi: 10.1006/exnr.1997.6713. Exp Neurol. 1998. PMID: 9454635
-
Transport and targeting of scrapie infectivity and pathology in the optic nerve projections following intraocular infection.Prog Clin Biol Res. 1989;317:645-52. Prog Clin Biol Res. 1989. PMID: 2513583 Review.
-
Scrapie in the central nervous system: neuroanatomical spread of infection and Sinc control of pathogenesis.J Gen Virol. 1992 Jul;73 ( Pt 7):1637-44. doi: 10.1099/0022-1317-73-7-1637. J Gen Virol. 1992. PMID: 1629695
-
Scrapie strain infection in vitro induces changes in neuronal cells.Mol Neurobiol. 1994 Apr-Jun;8(2-3):129-38. doi: 10.1007/BF02780663. Mol Neurobiol. 1994. PMID: 7999309 Review.
Cited by
-
Differential protein profiling as a potential multi-marker approach for TSE diagnosis.BMC Infect Dis. 2009 Nov 27;9:188. doi: 10.1186/1471-2334-9-188. BMC Infect Dis. 2009. PMID: 19943924 Free PMC article.
-
Cell Densities in the Mouse Brain: A Systematic Review.Front Neuroanat. 2018 Oct 23;12:83. doi: 10.3389/fnana.2018.00083. eCollection 2018. Front Neuroanat. 2018. PMID: 30405363 Free PMC article.
-
Identification of the end stage of scrapie using infected neural grafts.Brain Pathol. 1998 Jan;8(1):19-27. doi: 10.1111/j.1750-3639.1998.tb00130.x. Brain Pathol. 1998. PMID: 9458163 Free PMC article.
Publication types
MeSH terms
LinkOut - more resources
Full Text Sources