| Literature DB >> 24028895 |
Hiromi Kumon1, Eiji Matsuura2, Noriyuki Nagaoka3, Toshio Yamamoto3, Shinya Uehara4, Motoo Araki4, Yukana Matsunami2, Kazuko Kobayashi2, Akira Matsumoto4.
Abstract
The term nanobacteria, sometimes referred to as nanobacteria-like particles (NLPs), is presently recognized as a misnomer for inert calcified nanoparticles. However, misinterpretation of its propagation as a living organism still continues. Ultrastructural and elemental analyses, combining immuno-electron microscopy with an original NLP isolate (P-17) derived from urinary stones, and an IgM monoclonal antibody (CL-15) raised against P-17 have now revealed that, oxidized lipids with acidified functional groups were key elements in NLP propagation. Lamellar structures composed of acidic/oxidized lipids provided structural scaffolds for carbonate apatite crystals. During in vitro culture, lipid peroxidation induced by γ-irradiation of FBS was a major cause of accelerated NLP propagation. In pathological tissue samples from hyperlipidemic atherosclerosis-prone mice, CL-15 co-localized with fatty plaques, macrophage infiltrates and osteocalcin staining of aortic valve lesions. These observations indicate that naturally occurring NLP composed of mineralo-oxidized lipids complexes are generated as by-products rather than etiological agents of chronic inflammation. FROM THE CLINICAL EDITOR: The term "nanobacteria-like particles (NLPs)" is presently recognized as a misnomer for inert calcified nanoparticles as opposed to living organisms. This study convincingly demonstrates that naturally occurring NLPs composed of mineralo-oxidized lipid complexes are generated as by-products rather than etiological agents of chronic inflammation.Entities:
Keywords: Ectopic calcification; Nanobacteria-like particles; Nanoparticles; Oxidized lipids
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Year: 2013 PMID: 24028895 DOI: 10.1016/j.nano.2013.08.010
Source DB: PubMed Journal: Nanomedicine ISSN: 1549-9634 Impact factor: 5.307