Literature DB >> 28213849

Widespread Expression of a Membrane-Tethered Version of the Soluble Lysosomal Enzyme Palmitoyl Protein Thioesterase-1.

Charles Shyng1, Shannon L Macauley2, Joshua T Dearborn1, Mark S Sands3,4,5.   

Abstract

"Cross-correction," the transfer of soluble lysosomal enzymes between neighboring cells, forms the foundation for therapeutics of lysosomal storage disorders (LSDs). However, "cross-correction" poses a significant barrier to studying the role of specific cell types in LSD pathogenesis. By expressing the native enzyme in only one cell type, neighboring cell types are invariably corrected. In this study, we present a strategy to limit "cross-correction" of palmitoyl-protein thioesterase-1(PPT1), a lysosomal hydrolase deficient in Infantile Neuronal Ceroid Lipofuscinosis (INCL, Infantile Batten disease) to the lysosomal membrane via the C-terminus of lysosomal associated membrane protein-1 (LAMP1). Tethering PPT1 to the lysosomal membrane prevented "cross-correction" while allowing PPT1 to retain its enzymatic function and localization in vitro. A transgenic line harboring the lysosomal membrane-tethered PPT1 was then generated. We show that expression of lysosome-restricted PPT1 in vivo largely rescues the INCL biochemical, histological, and functional phenotype. These data suggest that lysosomal tethering of PPT1 via the C-terminus of LAMP1 is a viable strategy and that this general approach can be used to study the role of specific cell types in INCL pathogenesis, as well as other LSDs. Ultimately, understanding the role of specific cell types in the disease progression of LSDs will help guide the development of more targeted therapeutics. One Sentence Synopsis: Tethering PPT1 to the lysosomal membrane is a viable strategy to prevent "cross-correction" and will allow for the study of specific cellular contributions in INCL pathogenesis.

Entities:  

Keywords:  Infantile Batten disease; Lysosomal storage disorders; Neuronal ceroid lipofuscinosis; Palmitoyl-protein thioesterase-1; Soluble lysosomal enzymes

Year:  2017        PMID: 28213849      PMCID: PMC5680291          DOI: 10.1007/8904_2017_1

Source DB:  PubMed          Journal:  JIMD Rep        ISSN: 2192-8304


  32 in total

1.  Disruption of PPT1 or PPT2 causes neuronal ceroid lipofuscinosis in knockout mice.

Authors:  P Gupta; A A Soyombo; A Atashband; K E Wisniewski; J M Shelton; J A Richardson; R E Hammer; S L Hofmann
Journal:  Proc Natl Acad Sci U S A       Date:  2001-11-20       Impact factor: 11.205

2.  Successive neuron loss in the thalamus and cortex in a mouse model of infantile neuronal ceroid lipofuscinosis.

Authors:  Catherine Kielar; Lucy Maddox; Ellen Bible; Charlie C Pontikis; Shannon L Macauley; Megan A Griffey; Michael Wong; Mark S Sands; Jonathan D Cooper
Journal:  Neurobiol Dis       Date:  2006-10-12       Impact factor: 5.996

Review 3.  Overview: engineering transgenic constructs and mice.

Authors:  Naoto Haruyama; Andrew Cho; Ashok B Kulkarni
Journal:  Curr Protoc Cell Biol       Date:  2009-03

4.  Adeno-associated virus 2-mediated gene therapy decreases autofluorescent storage material and increases brain mass in a murine model of infantile neuronal ceroid lipofuscinosis.

Authors:  Megan Griffey; Ellen Bible; Carole Vogler; Beth Levy; Praveena Gupta; Jonathan Cooper; Mark S Sands
Journal:  Neurobiol Dis       Date:  2004-07       Impact factor: 5.996

5.  Lysosomal dysfunction results in altered energy balance.

Authors:  Josh C Woloszynek; Trey Coleman; Clay F Semenkovich; Mark S Sands
Journal:  J Biol Chem       Date:  2007-10-02       Impact factor: 5.157

6.  Proteomic Profiling in the Brain of CLN1 Disease Model Reveals Affected Functional Modules.

Authors:  Saara Tikka; Evanthia Monogioudi; Athanasios Gotsopoulos; Rabah Soliymani; Francesco Pezzini; Enzo Scifo; Kristiina Uusi-Rauva; Jaana Tyynelä; Marc Baumann; Anu Jalanko; Alessandro Simonati; Maciej Lalowski
Journal:  Neuromolecular Med       Date:  2015-12-26       Impact factor: 3.843

7.  The motif Tyr-X-X-hydrophobic residue mediates lysosomal membrane targeting of lysosome-associated membrane protein 1.

Authors:  F G Guarnieri; L M Arterburn; M B Penno; Y Cha; J T August
Journal:  J Biol Chem       Date:  1993-01-25       Impact factor: 5.157

8.  Cerebellar pathology and motor deficits in the palmitoyl protein thioesterase 1-deficient mouse.

Authors:  Shannon L Macauley; David F Wozniak; Catherine Kielar; Yun Tan; Jonathan D Cooper; Mark S Sands
Journal:  Exp Neurol       Date:  2009-02-10       Impact factor: 5.330

9.  In a model of Batten disease, palmitoyl protein thioesterase-1 deficiency is associated with brown adipose tissue and thermoregulation abnormalities.

Authors:  Alfia Khaibullina; Nicholas Kenyon; Virginia Guptill; Martha M Quezado; Li Wang; Deloris Koziol; Robert Wesley; Pablo R Moya; Zhongjian Zhang; Arjun Saha; Anil B Mukherjee; Zenaide M N Quezado
Journal:  PLoS One       Date:  2012-11-06       Impact factor: 3.240

10.  Comprehensive functional characterization of murine infantile Batten disease including Parkinson-like behavior and dopaminergic markers.

Authors:  Joshua T Dearborn; Steven K Harmon; Stephen C Fowler; Karen L O'Malley; George T Taylor; Mark S Sands; David F Wozniak
Journal:  Sci Rep       Date:  2015-08-04       Impact factor: 4.379

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  3 in total

1.  Cell-autonomous expression of the acid hydrolase galactocerebrosidase.

Authors:  Christina R Mikulka; Joshua T Dearborn; Bruno A Benitez; Amy Strickland; Lin Liu; Jeffrey Milbrandt; Mark S Sands
Journal:  Proc Natl Acad Sci U S A       Date:  2020-04-06       Impact factor: 11.205

2.  The Networks of Genes Encoding Palmitoylated Proteins in Axonal and Synaptic Compartments Are Affected in PPT1 Overexpressing Neuronal-Like Cells.

Authors:  Francesco Pezzini; Marzia Bianchi; Salvatore Benfatto; Francesca Griggio; Stefano Doccini; Rosalba Carrozzo; Arvydas Dapkunas; Massimo Delledonne; Filippo M Santorelli; Maciej M Lalowski; Alessandro Simonati
Journal:  Front Mol Neurosci       Date:  2017-08-22       Impact factor: 5.639

3.  Compromised astrocyte function and survival negatively impact neurons in infantile neuronal ceroid lipofuscinosis.

Authors:  Jenny Lange; Luke J Haslett; Emyr Lloyd-Evans; Jennifer M Pocock; Mark S Sands; Brenda P Williams; Jonathan D Cooper
Journal:  Acta Neuropathol Commun       Date:  2018-08-08       Impact factor: 7.801

  3 in total

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