Literature DB >> 31679100

In vitro cellular uptake and neuroprotective efficacy of poly-arginine-18 (R18) and poly-ornithine-18 (O18) peptides: critical role of arginine guanidinium head groups for neuroprotection.

Gabriella MacDougall1,2,3, Ryan S Anderton4,5,6, Eden Ouliel4,5, Junjie Gao4,7,8, Sharon L Redmond9,10, Neville W Knuckey11,4, Bruno P Meloni11,4,6.   

Abstract

We have previously demonstrated that Cationic Arginine-Rich Peptides (CARPs) and in particular poly-arginine-18 (R18; 18-mer of arginine) exhibit potent neuroprotective properties in both in vitro and in vivo neuronal injury models. Based on the current literature, there is a consensus that arginine residues by virtue of their positive charge and guanidinium head group is the critical element for imparting CARP neuroprotective properties and their ability to traverse cell membranes. This study examined the importance of guanidinium head groups in R18 for peptide cellular uptake, localization, and neuroprotection. This was achieved by using poly-ornithine-18 (O18; 18-mer of ornithine) as a control, which is structurally identical to R18, but possesses amino head groups rather than guanidino head groups. Epifluorescence and confocal fluorescence microscopy was used to examine the cellular uptake and localization of the FITC-conjugated R18 and O18 in primary rat cortical neurons and SH-SY5Y human neuroblastoma cell cultures. An in vitro cortical neuronal glutamic acid excitotoxicity model was used to compare the effectiveness of R18 and O18 to inhibit cell death and intracellular calcium influx, as well as caspase and calpain activation. Fluorescence imaging studies revealed cellular uptake of both FITC-R18 and FITC-O18 in neuronal and SH-SY5Y cells; however, intracellular localization of the peptides differed in neurons. Following glutamic acid excitotoxicity, only R18 was neuroprotective, prevented caspases and calpain activation, and was more effective at reducing neuronal intracellular calcium influx. Overall, this study demonstrated that for long chain cationic poly-arginine peptides, the guanidinium head groups provided by arginine residues are an essential requirement for neuroprotection but are not required for entry into neurons.

Entities:  

Keywords:  Excitotoxicity; Guanidinium; Neuroprotection; Poly-arginine; Poly-ornithine; R18

Mesh:

Substances:

Year:  2019        PMID: 31679100     DOI: 10.1007/s11010-019-03646-0

Source DB:  PubMed          Journal:  Mol Cell Biochem        ISSN: 0300-8177            Impact factor:   3.396


  71 in total

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Authors:  Bruno P Meloni; Laura M Brookes; Vince W Clark; Jane L Cross; Adam B Edwards; Ryan S Anderton; Richard M Hopkins; Katrin Hoffmann; Neville W Knuckey
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Journal:  Bioconjug Chem       Date:  2016-04-05       Impact factor: 4.774

6.  Assessment of the Neuroprotective Effects of Arginine-Rich Protamine Peptides, Poly-Arginine Peptides (R12-Cyclic, R22) and Arginine-Tryptophan-Containing Peptides Following In Vitro Excitotoxicity and/or Permanent Middle Cerebral Artery Occlusion in Rats.

Authors:  Bruno P Meloni; Diego Milani; Jane L Cross; Vince W Clark; Adam B Edwards; Ryan S Anderton; David J Blacker; Neville W Knuckey
Journal:  Neuromolecular Med       Date:  2017-05-18       Impact factor: 3.843

7.  Apelin, an endogenous neuronal peptide, protects hippocampal neurons against excitotoxic injury.

Authors:  Lauren A O'Donnell; Arpita Agrawal; Praveena Sabnekar; Marc A Dichter; David R Lynch; Dennis L Kolson
Journal:  J Neurochem       Date:  2007-09       Impact factor: 5.372

8.  Antennapedia and HIV transactivator of transcription (TAT) "protein transduction domains" promote endocytosis of high molecular weight cargo upon binding to cell surface glycosaminoglycans.

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Journal:  J Biol Chem       Date:  2003-06-30       Impact factor: 5.157

9.  An atypical role for collapsin response mediator protein 2 (CRMP-2) in neurotransmitter release via interaction with presynaptic voltage-gated calcium channels.

Authors:  Joel M Brittain; Andrew D Piekarz; Yuying Wang; Takako Kondo; Theodore R Cummins; Rajesh Khanna
Journal:  J Biol Chem       Date:  2009-09-15       Impact factor: 5.157

10.  Antidiabetic Drug Metformin Protects Neuronal Cells against Quinolinic Acid-Induced Excitotoxicity by Decreasing Intracellular Calcium.

Authors:  Sujeong Jang; Sah-Hoon Park
Journal:  Chonnam Med J       Date:  2018-01-25
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