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Exceptional in vivo catabolism of neurodegeneration-related aggregates

Authors :
Zsolt Datki
Lívia Fülöp
Zsolt Bozsó
Amanda Szarvas
János Kálmán
Lilla Mácsai
Bence Galik
Katalin Zsuga
Zita Oláh
Éva Ács
Angéla Földi
Tibor Hortobágyi
Source :
Acta Neuropathologica Communications, Vol 6, Iss 1, Pp 1-12 (2018), Acta Neuropathologica Communications
Publication Year :
2018
Publisher :
BMC, 2018.

Abstract

Neurodegenerative diseases are linked to a systemic enzyme resistance of toxic aggregated molecules and their pathological consequences. This paper presents a unique phenomenon that Philodina acuticornis, a bdelloid rotifer, is able to catabolize different types of neurotoxic peptide and protein aggregates (such as beta-amyloids /Aβ/, alpha-synuclein, and prion) without suffering any damage. P. acuticornis is capable of using these aggregates as an exclusive energy source (i.e., as ‘food’, identified in the digestive system and body) in a hermetically isolated microdrop environment, increasing their survival. As regards Aβ1–42, five other bdelloid rotifer species were also found to be able to perform this phenomenon. Based on our experiments, the Aβ1–42-treated bdelloid rotifers demonstrate significantly increased survival (e.g. mean lifespan = 51 ± 2.71 days) compared to their untreated controls (e.g. mean lifespan = 14 ± 2.29 days), with similar improvements in a variety of phenotypic characteristics. To our knowledge, no other animal species have so far been reported to have a similar capability. For all other microscopic species tested, including monogonant rotifers and non-rotifers, the treatment with Aβ1–42 aggregates proved to be either toxic or simply ineffective. This paper describes and proves the existence of an unprecedented in vivo catabolic capability of neurotoxic aggregates by bdelloid rotifers, with special focus on P. acuticornis. Our results may provide the basis for a new preclinical perspective on therapeutic research in human neurodegenerative diseases.

Details

Language :
English
ISSN :
20515960
Volume :
6
Issue :
1
Database :
OpenAIRE
Journal :
Acta Neuropathologica Communications
Accession number :
edsair.doi.dedup.....420e405addef95ec870a7e82eb7fa1ed