Literature DB >> 8583832

Age-related changes in cellular localization and enzymatic activities of cathepsins B, L and D in the rat trigeminal ganglion neuron.

T Amano1, H Nakanishi, T Kondo, T Tanaka, M Oka, K Yamamoto.   

Abstract

Altered localization and cellular level of three distinct lysosomal proteinases, cathepsins B (CB), L (CL), and D (CD), with aging were investigated in the rat trigeminal ganglion (TG) by immunohistochemical and quantitative analyses. At the light microscopic level, the intracytoplasmic distribution of these three enzymes was found to change with aging: These lysosomal proteinases in the TG of young rats (2-3 months of age) were widely and evenly distributed throughout the cytoplasm as coarse intracytoplasmic granules, whereas they were localized at focal cytoplasmic sites of the TG neurons of aged rats (28-31 months of age) as coarse aggregates. A similar distribution was observed with a major lysosomal membrane sialoglycoprotein having an apparent molecular mass of 107 kDa (LGP107). The cellular distribution of the three cathepsins as well as LGP107 in the TG neurons of aged rats corresponded well with that of autofluorescent lipofuscin. At the electron microscopic level, the age-related redistribution of these cathepsins in the TG neurons was found to be due to their great accumulation in autolysosomes localized at the focal perinuclear sites. The cellular levels of CB and CL determined by activity measurement in the TG of the young rats were 1.8 and 1.7 times as much as those of the aged rats respectively. In contrast, no significant difference was observed between the CD activities in the two age groups. These results strongly suggest that age related changes in localization and cellular level of CB, CL, and CD in TG neurons are closely linked with the increased formation of autolysosomes and lipofuscins, which is the most ubiquitous age-related cytological alteration.

Entities:  

Mesh:

Substances:

Year:  1995        PMID: 8583832     DOI: 10.1016/0047-6374(95)01615-7

Source DB:  PubMed          Journal:  Mech Ageing Dev        ISSN: 0047-6374            Impact factor:   5.432


  7 in total

1.  Cultured porcine trabecular meshwork cells display altered lysosomal function when subjected to chronic oxidative stress.

Authors:  Paloma B Liton; Yizhi Lin; Coralia Luna; Guorong Li; Pedro Gonzalez; David L Epstein
Journal:  Invest Ophthalmol Vis Sci       Date:  2008-05-09       Impact factor: 4.799

2.  Alteration of cathepsins and actin genes expression in rat brain during ageing.

Authors:  N L Rendakov; L V Topchieva; I A Vinogradova; N N Nemova
Journal:  Dokl Biol Sci       Date:  2011-03-05

3.  Granulovacuolar degeneration (GVD) bodies of Alzheimer's disease (AD) resemble late-stage autophagic organelles.

Authors:  K E Funk; R E Mrak; J Kuret
Journal:  Neuropathol Appl Neurobiol       Date:  2011-04       Impact factor: 8.090

4.  Preferential MyoD homodimer formation demonstrated by a general method of dominant negative mutation employing fusion with a lysosomal protease.

Authors:  F Q Li; A Coonrod; M Horwitz
Journal:  J Cell Biol       Date:  1996-11       Impact factor: 10.539

Review 5.  Cysteine cathepsins in neurological disorders.

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

Review 6.  Oxidative stress and autophagy in the regulation of lysosome-dependent neuron death.

Authors:  Violetta N Pivtoraiko; Sara L Stone; Kevin A Roth; John J Shacka
Journal:  Antioxid Redox Signal       Date:  2009-03       Impact factor: 8.401

7.  Endogenous angiotensinergic system in neurons of rat and human trigeminal ganglia.

Authors:  Hans Imboden; Jaspal Patil; Juerg Nussberger; Françoise Nicoud; Benno Hess; Nermin Ahmed; Thomas Schaffner; Maren Wellner; Dominik Müller; Tadashi Inagami; Takaaki Senbonmatsu; Jaroslav Pavel; Juan M Saavedra
Journal:  Regul Pept       Date:  2009-02-12
  7 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.