| Literature DB >> 23876822 |
Tomohiro Itoh1, Ryosuke Tsuzuki, Toshiomi Tanaka, Masayuki Ninomiya, Yuji Yamaguchi, Hiroyuki Takenaka, Masashi Ando, Yasuyuki Tsukamasa, Mamoru Koketsu.
Abstract
Nostoc commune is a terrestrial benthic blue-green alga that often forms an extended mucilaginous layer on the soil, accumulates on stones and mud in aquatic environments. Reduced-scytonemin (R-scy), isolated from N. commune Vaucher, has been shown to suppress the human T-lymphoid Jurkat cell growth. To reveal the mechanisms underlying the R-scy-mediated inhibition of Jurkat cell growth, we examined cell morphology, DNA fragmentation, and microtubule-associated protein light chain 3 (LC3) modification in these cells. We observed multiple vacuoles as well as the conversion of LC3-I to LC3-II in R-scy-treated cells. These results suggest that the R-scy induced Jurkat cell growth inhibition is attributable to the induction of type II programmed cell death (PCD II; autophagic cell death or autophagy). We further examined the mechanisms underlying R-scy-induced PCDII. The cells treated with R-scy produced large amounts of reactive oxygen species (ROS), leading to the induction of mitochondrial dysfunction. However, the elimination of R-scy-induced ROS by treatment with N-acetyl-L-cysteine (NAC) markedly opposed R-scy-induced PCDII. Based on these results, we conclude that ROS formation plays a critical role in R-scy-induced PCDII.Entities:
Keywords: Autophagy; Intracellular ROS; Nostoc commune Vauch; Reduced scytonemin; Type II programmed cell death
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Year: 2013 PMID: 23876822 DOI: 10.1016/j.fct.2013.07.016
Source DB: PubMed Journal: Food Chem Toxicol ISSN: 0278-6915 Impact factor: 6.023