» Articles » PMID: 7494600

Distribution of Tangles and Threads in the Cerebral Cortex in Progressive Supranuclear Palsy

Overview
Specialty Neurology
Date 1995 Aug 1
PMID 7494600
Citations 9
Authors
Affiliations
Soon will be listed here.
Abstract

Recent studies have described silver- and tau-positive glia and threads in the degenerating lesions of progressive supranuclear palsy. In this study, Gallyas-Braak silver impregnation and several immunohistochemical techniques were employed to examine the distribution of tangles, abnormal glia and threads in the cerebral cortex of nine cases of progressive supranuclear palsy. In addition to neurofibrillary tangles, argentophilic glia and threads were impregnated exclusively by Gallyas-Braak technique. This technique demonstrated two types of glia profiles: tightly coiled intra-cytoplasmic profiles surrounding nuclei (coiled profiles) and thorn-like profiles with radial ramifications (thorn-like profiles). Thorn-like profiles are possibly in astrocytes and were detected in the cerebral cortex, while coiled profiles are possibly in oligodendroglia and were detected both in the cerebral cortex and subcortical white matter. Topographically, many neurofibrillary tangles were constantly seen in the frontal cortex and in the pre-central gyrus. Numerous neurofibrillary tangles were detected in the entorhinal cortex of the two brains. Argentophilic glia and threads were also frequent both in the frontal cortex and the precentral gyrus; however, they were more frequent in the pre-central gyrus that in the frontal cortex in four of the eight cases examined. In two brains, argentophilic threads were distributed widely in the cerebral cortex and white matter except for the temporal cortex. In immunohistochemical studies, argentophilic glia and threads were mostly positive for Tau 2, and a small number of them were weakly positive for ubiquitin and paired helical filament protein. The immunoproperties of these abnormal glia and threads seemed to be virtually identical to those of neurofibrillary tangles.(ABSTRACT TRUNCATED AT 250 WORDS)

Citing Articles

Neuropsychological study of amyotrophic lateral sclerosis and parkinsonism-dementia complex in Kii peninsula, Japan.

Shindo A, Ueda Y, Kuzuhara S, Kokubo Y BMC Neurol. 2014; 14:151.

PMID: 25041813 PMC: 4107997. DOI: 10.1186/1471-2377-14-151.


RETRACTED: Wild type and P301L mutant Tau promote neuro-inflammation and α-Synuclein accumulation in lentiviral gene delivery models.

Khandelwal P, Dumanis S, Herman A, Rebeck G, Moussa C Mol Cell Neurosci. 2011; 49(1):44-53.

PMID: 21945393 PMC: 3246111. DOI: 10.1016/j.mcn.2011.09.002.


The relationship between clinical and pathological variables in Richardson's syndrome.

Schofield E, Hodges J, Bak T, Xuereb J, Halliday G J Neurol. 2011; 259(3):482-90.

PMID: 21837549 DOI: 10.1007/s00415-011-6205-8.


The Relationship between Parkin and Protein Aggregation in Neurodegenerative Diseases.

Khandelwal P, Moussa C Front Psychiatry. 2011; 1:15.

PMID: 21423426 PMC: 3059628. DOI: 10.3389/fpsyt.2010.00015.


β-amyloid triggers ALS-associated TDP-43 pathology in AD models.

Herman A, Khandelwal P, Stanczyk B, Rebeck G, Moussa C Brain Res. 2011; 1386:191-9.

PMID: 21376022 PMC: 3073036. DOI: 10.1016/j.brainres.2011.02.052.