Literature DB >> 21815999

Increased glucose concentration results in reduced proteasomal activity and the formation of glycogen positive aggresomal structures.

Rajat Puri1, Navodita Jain, Subramaniam Ganesh.   

Abstract

Recent studies indicate that glycogen, besides being a principal storage product, confers protection against cellular stress through an unknown physiological pathway. Abnormal glycogen inclusions have also been considered to underlie pathology in a few neurodegenerative disorders that are caused by proteolytic dysfunctions, although a link between proteolytic pathways and glycogen accumulation is yet to be established. In the present study, we investigated the subcellular localization of glycogen particles and report that their distribution is altered under physiological stress. Using a cellular model, we show that glycogen particles are recruited to the centrosomal aggresomal structures upon proteasomal or lysosomal blockade, and that this recruitment is dependent on the microtubule function. We also show that an increase in the glucose concentration leads to decreased cellular proteasomal activity and the formation of glycogen positive aggresomal structures. Proteasomal blockade also leads to the formation of diastase-resistant polyglucosan bodies. The glycogen particles in aggresomes might provide energy to the proteolytic process and/or function as a scaffold. Taken together, the findings of the present study suggest a functional link between proteasomal function and polyglucosan bodies, and also suggest that these two physiological processes could be linked in neurodegenerative disorders.
© 2011 The Authors Journal compilation © 2011 FEBS.

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Year:  2011        PMID: 21815999     DOI: 10.1111/j.1742-4658.2011.08287.x

Source DB:  PubMed          Journal:  FEBS J        ISSN: 1742-464X            Impact factor:   5.542


  8 in total

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Authors:  Giovanna Cenacchi; V Papa; R Costa; V Pegoraro; R Marozzo; M Fanin; C Angelini
Journal:  Virchows Arch       Date:  2019-07-30       Impact factor: 4.064

2.  Polyubiquitinated proteins, proteasome, and glycogen characterize the particle-rich cytoplasmic structure (PaCS) of neoplastic and fetal cells.

Authors:  Vittorio Necchi; Patrizia Sommi; Agostina Vitali; Alessandro Vanoli; Anna Savoia; Vittorio Ricci; Enrico Solcia
Journal:  Histochem Cell Biol       Date:  2014-03-01       Impact factor: 4.304

3.  Decreased O-linked GlcNAcylation protects from cytotoxicity mediated by huntingtin exon1 protein fragment.

Authors:  Amit Kumar; Pankaj Kumar Singh; Rashmi Parihar; Vibha Dwivedi; Subhash C Lakhotia; Subramaniam Ganesh
Journal:  J Biol Chem       Date:  2014-03-19       Impact factor: 5.157

4.  PaCS is a novel cytoplasmic structure containing functional proteasome and inducible by cytokines/trophic factors.

Authors:  Patrizia Sommi; Vittorio Necchi; Agostina Vitali; Daniela Montagna; Ada De Luigi; Mario Salmona; Vittorio Ricci; Enrico Solcia
Journal:  PLoS One       Date:  2013-12-17       Impact factor: 3.240

5.  Glycogen synthase protects neurons from cytotoxicity of mutant huntingtin by enhancing the autophagy flux.

Authors:  Anupama Rai; Pankaj Kumar Singh; Virender Singh; Vipendra Kumar; Rohit Mishra; Ashwani Kumar Thakur; Anita Mahadevan; Susarla Krishna Shankar; Nihar Ranjan Jana; Subramaniam Ganesh
Journal:  Cell Death Dis       Date:  2018-02-08       Impact factor: 8.469

6.  Alterations in brain glycogen levels influence life-history traits and reduce the lifespan in female Drosophila melanogaster.

Authors:  Deepashree Sheshadri; Akanksha Onkar; Subramaniam Ganesh
Journal:  Biol Open       Date:  2021-12-14       Impact factor: 2.422

7.  A Micro-Scale Analytical Method for Determining Glycogen Turnover by NMR and FTMS.

Authors:  Timothy L Scott; Juan Zhu; Teresa A Cassel; Sara Vicente-Muñoz; Penghui Lin; Richard M Higashi; Andrew N Lane; Teresa W-M Fan
Journal:  Metabolites       Date:  2022-08-18

Review 8.  Glycogen metabolism has a key role in the cancer microenvironment and provides new targets for cancer therapy.

Authors:  Christos E Zois; Adrian L Harris
Journal:  J Mol Med (Berl)       Date:  2016-02-17       Impact factor: 4.599

  8 in total

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