Literature DB >> 20202124

HtrA2/Omi-immunoreactive intraneuronal inclusions in the anterior horn of patients with sporadic and Cu/Zn superoxide dismutase (SOD1) mutant amyotrophic lateral sclerosis.

Y Kawamoto1, H Ito, Y Kobayashi, Y Suzuki, I Akiguchi, H Fujimura, S Sakoda, H Kusaka, A Hirano, R Takahashi.   

Abstract

AIMS: HtrA2/Omi is a mitochondrial serine protease that promotes the apoptotic processes, but the relationship between HtrA2/Omi and amyotrophic lateral sclerosis (ALS) is still unknown. The purpose of the present study was to determine whether abnormal expression of HtrA2/Omi occurs in patients with ALS.
METHODS: We prepared autopsied spinal cord tissues from 7 control subjects, 11 patients with sporadic ALS (SALS) and 4 patients with Cu/Zn superoxide dismutase (SOD1)-related familial ALS (FALS). We then performed immunohistochemical studies on HtrA2/Omi using formalin-fixed, paraffin-embedded sections from all of the cases.
RESULTS: In the control subjects, the anterior horn cells were mildly to moderately immunostained with HtrA2/Omi. In the patients with SALS, strong HtrA2/Omi immunoreactivity was found in some skein-like inclusions and round hyaline inclusions as well as many spheroids, but Bunina bodies were immunonegative for HtrA2/Omi. In the patients with SOD1-related FALS, Lewy body-like hyaline inclusions were observed in three cases and conglomerate inclusions were observed in the remaining case, and both types of inclusions were intensely immunopositive for HtrA2/Omi.
CONCLUSIONS: These results suggest that abnormal accumulations of HtrA2/Omi may occur in several types of motor neuronal inclusions in the anterior horn from SALS and SOD1-linked FALS cases, and that HtrA2/Omi may be associated with the pathogenesis of both types of ALS.

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Year:  2010        PMID: 20202124     DOI: 10.1111/j.1365-2990.2010.01075.x

Source DB:  PubMed          Journal:  Neuropathol Appl Neurobiol        ISSN: 0305-1846            Impact factor:   8.090


  4 in total

1.  Dysregulated expression of death, stress and mitochondrion related genes in the sciatic nerve of presymptomatic SOD1(G93A) mouse model of Amyotrophic Lateral Sclerosis.

Authors:  Chrystian J Alves; Jessica R Maximino; Gerson Chadi
Journal:  Front Cell Neurosci       Date:  2015-09-01       Impact factor: 5.505

2.  Omi inhibition ameliorates neuron apoptosis and neurological deficit after subarachnoid hemorrhage in rats.

Authors:  Yuanfeng Du; Dingbo Yang; Xiaoqiao Dong; Quan Du; Ding Wang; Yongfeng Shen; Wenhua Yu
Journal:  Genes Genomics       Date:  2021-10-22       Impact factor: 1.839

3.  Sex specific activation of the ERα axis of the mitochondrial UPR (UPRmt) in the G93A-SOD1 mouse model of familial ALS.

Authors:  Amanjot K Riar; Suzanne R Burstein; Gloria M Palomo; Andrea Arreguin; Giovanni Manfredi; Doris Germain
Journal:  Hum Mol Genet       Date:  2017-04-01       Impact factor: 5.121

4.  Gene expression profiling for human iPS-derived motor neurons from sporadic ALS patients reveals a strong association between mitochondrial functions and neurodegeneration.

Authors:  Chrystian J Alves; Rafael Dariolli; Frederico M Jorge; Matheus R Monteiro; Jessica R Maximino; Roberto S Martins; Bryan E Strauss; José E Krieger; Dagoberto Callegaro; Gerson Chadi
Journal:  Front Cell Neurosci       Date:  2015-08-04       Impact factor: 5.505

  4 in total

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