Reactive astrocytes are widespread in the cortical gray matter of amyotrophic lateral sclerosis - PubMed (original) (raw)
. 1994 Jun 15;38(3):336-47.
doi: 10.1002/jnr.490380312.
Affiliations
- PMID: 7523689
- DOI: 10.1002/jnr.490380312
Reactive astrocytes are widespread in the cortical gray matter of amyotrophic lateral sclerosis
D Nagy et al. J Neurosci Res. 1994.
Abstract
The distribution of reactive astrocytes was examined in the cortical gray matter of non-motor and motor regions from cases of familial and sporadic amyotrophic lateral sclerosis (ALS) and compared to that of beta-amyloid deposits. By glial fibrillary acidic protein immunocytochemistry, patches of reactive astrocytes, characterized by multiple reactive astrocytes in a circular or patch-like formation, occurred in 12 of 15 ALS cases examined. These patches of reactive astrocytes were not restricted to the motor cortex but were found in the gray matter in ALS in all examined brain regions, including frontal, temporal, inferior parietal, cingulate, occipital, and motor cortices, from both familial and sporadic ALS cases. Reactive astrocytes were also found in the subpial region and at the gray/white matter junction. Because patches of astrocytes can occur in association with senile plaques, beta-amyloid was localized. By immunostaining, beta-amyloid deposits were observed in five of the 15 ALS cases: three cases had only early plaques, two had both early and classic plaques. The number of ALS cases with both astrocyte patches and amyloid plaques was four of 15, but typically astrocyte patches in ALS occurred without any evidence of an association with beta-amyloid deposits. Therefore, the astrocyte patches in ALS are not the result of beta-amyloid deposition. The widespread occurrence of reactive astrocytes, as patches in the cortical gray matter and in the subpial region and at the gray/white matter junction, is evidence of a widespread pathology in ALS cortex in both familial and sporadic forms of the disease.
Similar articles
- Alzheimer disease pathology in amyotrophic lateral sclerosis.
Hamilton RL, Bowser R. Hamilton RL, et al. Acta Neuropathol. 2004 Jun;107(6):515-22. doi: 10.1007/s00401-004-0843-1. Epub 2004 Mar 16. Acta Neuropathol. 2004. PMID: 15024584 - Differential damage in the frontal cortex with aging, sporadic and familial Alzheimer's disease.
Leuba G, Vernay A, Zimmermann V, Saini K, Kraftsik R, Savioz A. Leuba G, et al. Brain Res Bull. 2009 Oct 28;80(4-5):196-202. doi: 10.1016/j.brainresbull.2009.06.009. Epub 2009 Jun 25. Brain Res Bull. 2009. PMID: 19559767 - Beta-amyloid 42 accumulation in the lumbar spinal cord motor neurons of amyotrophic lateral sclerosis patients.
Calingasan NY, Chen J, Kiaei M, Beal MF. Calingasan NY, et al. Neurobiol Dis. 2005 Jun-Jul;19(1-2):340-7. doi: 10.1016/j.nbd.2005.01.012. Neurobiol Dis. 2005. PMID: 15837590 - [Amyotrophic lateral sclerosis: is the astrocyte the cell primarily involved?].
Sica RE. Sica RE. Medicina (B Aires). 2013;73(6):573-8. Medicina (B Aires). 2013. PMID: 24356272 Review. Spanish. - Examining the relationship between astrocyte dysfunction and neurodegeneration in ALS using hiPSCs.
Halpern M, Brennand KJ, Gregory J. Halpern M, et al. Neurobiol Dis. 2019 Dec;132:104562. doi: 10.1016/j.nbd.2019.104562. Epub 2019 Aug 2. Neurobiol Dis. 2019. PMID: 31381978 Free PMC article. Review.
Cited by
- Motoneuron Diseases.
Lotti F, Przedborski S. Lotti F, et al. Adv Neurobiol. 2022;28:323-352. doi: 10.1007/978-3-031-07167-6_13. Adv Neurobiol. 2022. PMID: 36066831 - Targeting TNFα produced by astrocytes expressing amyotrophic lateral sclerosis-linked mutant fused in sarcoma prevents neurodegeneration and motor dysfunction in mice.
Jensen BK, McAvoy KJ, Heinsinger NM, Lepore AC, Ilieva H, Haeusler AR, Trotti D, Pasinelli P. Jensen BK, et al. Glia. 2022 Jul;70(7):1426-1449. doi: 10.1002/glia.24183. Epub 2022 Apr 26. Glia. 2022. PMID: 35474517 Free PMC article. - Tumor Necrosis Factor Alpha in Amyotrophic Lateral Sclerosis: Friend or Foe?
Guidotti G, Scarlata C, Brambilla L, Rossi D. Guidotti G, et al. Cells. 2021 Mar 1;10(3):518. doi: 10.3390/cells10030518. Cells. 2021. PMID: 33804386 Free PMC article. Review. - The neuropathological signature of bulbar-onset ALS: A systematic review.
Shellikeri S, Karthikeyan V, Martino R, Black SE, Zinman L, Keith J, Yunusova Y. Shellikeri S, et al. Neurosci Biobehav Rev. 2017 Apr;75:378-392. doi: 10.1016/j.neubiorev.2017.01.045. Epub 2017 Feb 2. Neurosci Biobehav Rev. 2017. PMID: 28163193 Free PMC article. Review. - Alterations in lipid metabolism of spinal cord linked to amyotrophic lateral sclerosis.
Chaves-Filho AB, Pinto IFD, Dantas LS, Xavier AM, Inague A, Faria RL, Medeiros MHG, Glezer I, Yoshinaga MY, Miyamoto S. Chaves-Filho AB, et al. Sci Rep. 2019 Aug 12;9(1):11642. doi: 10.1038/s41598-019-48059-7. Sci Rep. 2019. PMID: 31406145 Free PMC article.
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Medical
Miscellaneous