Literature DB >> 8157122

Age-related changes in activities and localizations of cathepsins D, E, B, and L in the rat brain tissues.

H Nakanishi1, K Tominaga, T Amano, I Hirotsu, T Inoue, K Yamamoto.   

Abstract

Altered cellular levels and localizations of four distinct intracellular proteinases, cathepsins D, E, B, and L, with aging were studied in various rat brain tissues by enzymatic and immunohistochemical methods using discriminative antibodies specific for each enzyme. With regard to two aspartic proteinases, cathepsin E was barely detectable in all the brain tissues of young adult rats, including the cerebral cortex, the hippocampus, the neostriatum, and the cerebellum, whereas cathepsin D was ubiquitously found in these tissues. Two cysteine proteinases, cathepsins B and L, also existed in these tissues of young rats at the relatively high levels of activities. In aged rats, the cathepsin D levels in all of the brain tissues examined were about twice those of young rats. Cathepsin E was markedly increased in the cerebral cortex and neostriatum of aged rats, but not in the other tissues. The levels of cathepsin B were also increased significantly in the neostriatum of aged rats, but not significantly in the other tissues. In contrast, the activity levels of cathepsin L were strikingly decreased in all the brain tissues of aged rats. At the light microscopic level, the increased immunoreactivity of cathepsins D and E in the brain tissues of aged rats was eminent in both the neurons and the glial cells. By double-immunostaining technique, the cathepsin D-positive glial cells were mainly associated with reactive astrocytes, whereas the cathepsin E-positive glial cells were largely reactive microglial cells. Western blot analyses revealed that the molecular forms of cathepsins D and E increasingly expressed in the cerebral cortex of aged rats were similar to those of the respective normal mature enzymes. The increased immunoreactivity of cathepsin B in the neostriatum of aged rats was also found in both the neurons and the glial cells. Despite the marked decrease of the cathepsin L activity in various brain tissues of aged rats, the immunostaining for this enzyme was not significantly changed, indicating the occurrence of the catalytically inactive form of the enzyme in these tissues. These results suggest that the increased levels of cathepsins D, E, and B and the decrease in cathepsin L activity in brain regions of aged rats are related to both the neuronal degeneration and the reactivation of glial cells during the normal aging process of the brain.

Entities:  

Mesh:

Substances:

Year:  1994        PMID: 8157122     DOI: 10.1006/exnr.1994.1048

Source DB:  PubMed          Journal:  Exp Neurol        ISSN: 0014-4886            Impact factor:   5.330


  34 in total

1.  Cathepsin D deficiency induces lysosomal storage with ceroid lipofuscin in mouse CNS neurons.

Authors:  M Koike; H Nakanishi; P Saftig; J Ezaki; K Isahara; Y Ohsawa; W Schulz-Schaeffer; T Watanabe; S Waguri; S Kametaka; M Shibata; K Yamamoto; E Kominami; C Peters; K von Figura; Y Uchiyama
Journal:  J Neurosci       Date:  2000-09-15       Impact factor: 6.167

2.  Suppression of cathepsins B and L causes a proliferation of lysosomes and the formation of meganeurites in hippocampus.

Authors:  E Bednarski; C E Ribak; G Lynch
Journal:  J Neurosci       Date:  1997-06-01       Impact factor: 6.167

3.  Cerebrospinal fluid cathepsin B and S.

Authors:  Elin Nilsson; Constantin Bodolea; Torsten Gordh; Anders Larsson
Journal:  Neurol Sci       Date:  2012-03-23       Impact factor: 3.307

4.  The cysteine protease inhibitor, E64d, reduces brain amyloid-β and improves memory deficits in Alzheimer's disease animal models by inhibiting cathepsin B, but not BACE1, β-secretase activity.

Authors:  Gregory Hook; Vivian Hook; Mark Kindy
Journal:  J Alzheimers Dis       Date:  2011       Impact factor: 4.472

5.  Lysosomal proteolysis and autophagy require presenilin 1 and are disrupted by Alzheimer-related PS1 mutations.

Authors:  Ju-Hyun Lee; W Haung Yu; Asok Kumar; Sooyeon Lee; Panaiyur S Mohan; Corrinne M Peterhoff; Devin M Wolfe; Marta Martinez-Vicente; Ashish C Massey; Guy Sovak; Yasuo Uchiyama; David Westaway; Ana Maria Cuervo; Ralph A Nixon
Journal:  Cell       Date:  2010-06-10       Impact factor: 41.582

6.  The Critical Role of Proteolytic Relay through Cathepsins B and E in the Phenotypic Change of Microglia/Macrophage.

Authors:  Junjun Ni; Zhou Wu; Christoph Peterts; Kenji Yamamoto; Hong Qing; Hiroshi Nakanishi
Journal:  J Neurosci       Date:  2015-09-09       Impact factor: 6.167

7.  Involvement of nitric oxide released from microglia-macrophages in pathological changes of cathepsin D-deficient mice.

Authors:  H Nakanishi; J Zhang; M Koike; T Nishioku; Y Okamoto; E Kominami; K von Figura; C Peters; K Yamamoto; P Saftig; Y Uchiyama
Journal:  J Neurosci       Date:  2001-10-01       Impact factor: 6.167

8.  Calcium-evoked dendritic exocytosis in cultured hippocampal neurons. Part I: trans-Golgi network-derived organelles undergo regulated exocytosis.

Authors:  M Maletic-Savatic; R Malinow
Journal:  J Neurosci       Date:  1998-09-01       Impact factor: 6.167

9.  The ketogenic diet suppresses the cathepsin E expression induced by kainic acid in the rat brain.

Authors:  Hyun Jeong Jeong; Hojeong Kim; Yoon-Kyoung Kim; Sang-Kyu Park; Dong-Won Kang; Dojun Yoon
Journal:  Yonsei Med J       Date:  2010-09       Impact factor: 2.759

Review 10.  Cysteine cathepsins in neurological disorders.

Authors:  Anja Pišlar; Janko Kos
Journal:  Mol Neurobiol       Date:  2013-11-15       Impact factor: 5.590

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.