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1.
Food Funct ; 13(23): 12451-12452, 2022 Nov 28.
Article in English | MEDLINE | ID: mdl-36341848

ABSTRACT

Correction for 'Polysaccharides from Ulva prolifera O.F. Müller inhibit cell proliferation via activating MAPK signaling in A549 and H1650 cells' by Juan Juan Yang et al., Food Funct., 2021, 12, 6915-6924, https://doi.org/10.1039/D1FO00294E.

2.
Food Funct ; 12(15): 6915-6924, 2021 Aug 02.
Article in English | MEDLINE | ID: mdl-34132294

ABSTRACT

Reactive oxygen species (ROS), especially hydrogen peroxide (H2O2), have recently been reported to cause a significant increase in the production and expression of matrix metalloproteinases (MMPs), which are closely correlated with lung cancer metastasis. The aim of the present study is to determine the inhibitory effects of a polysaccharide isolated from Ulva prolifera O.F. Müller (U. prolifera) on the invasive potential of non-small cell lung cancer (NSCLC) cells, and further to explore the underlying mechanisms connected to that potential. The data showed that increased MMP-9 resulting from H2O2 exposure was mediated by activating mitogen-activated protein kinases (MAPKs). Pre-treatment with polysaccharides suppressed the activation of H2O2-mediated MAPK pathways and cell invasion. Hence, MMP-9 production triggered by H2O2 was demonstrated by activating MAPK signaling in a Myc-dependent manner. Taken together, these results suggested that polysaccharides suppress H2O2-induced cell invasion by inhibiting Myc-mediated MMP-9 gene transcription through the MAPK signaling pathway in A549 and NCI-H1650 cells. Our data also suggested that polysaccharides may be useful in minimizing the development of lung cancer metastasis. In the future, pretreatment with polysaccharides because of their antioxidant properties might be beneficial to enhance surgical outcomes.


Subject(s)
Cell Proliferation/drug effects , MAP Kinase Signaling System/drug effects , Plant Extracts/pharmacology , Polysaccharides/pharmacology , Ulva/chemistry , A549 Cells , Cell Line, Tumor , Humans , Hydrogen Peroxide/pharmacology , Matrix Metalloproteinase 9/metabolism
3.
Planta ; 235(5): 885-93, 2012 May.
Article in English | MEDLINE | ID: mdl-22101945

ABSTRACT

Porphyra yezoensis has a macroscopic foliage gametophyte phase with only a single cell layer, and is ideally suited for the study of the sexual differentiation process, from the vegetative cell to the spermatia. Firstly, we compared variations in the responses of the vegetative and male sectors to desiccation. Later, cell tracking experiments were carried out during the formation of spermatia from vegetative cells. The two sectors showed similar tolerance to desiccation, and the formation of spermatia from vegetative cells was independent of the degree of desiccation. Both light and scanning electron microscopy (SEM) observations of the differentiation process showed that the formation of spermatia could be divided into six phases: the one-cell, two-cell, four-cell, eight-cell, pre-release and spermatia phases. Photomicrographs of Fluorescent Brightener staining showed that the released spermatia had no cell walls. Photosynthetic data showed that there was a significant rise in Y(II) in the four-cell phase, indicating an increase in photosynthetic efficiency of PSII during this phase. We propose that this photosynthetic rise may be substantial and provide the increased energy needed for the formation and release of spermatia in P. yezoensis.


Subject(s)
Acclimatization/physiology , Germ Cells, Plant/cytology , Germ Cells, Plant/growth & development , Photosynthesis/physiology , Plant Cells/physiology , Porphyra/cytology , Porphyra/physiology , Aquatic Organisms/physiology , Cell Differentiation , China , Desiccation , Droughts , Sex Differentiation/physiology , Water/metabolism
4.
Sheng Wu Gong Cheng Xue Bao ; 21(4): 530-3, 2005 Jul.
Article in Chinese | MEDLINE | ID: mdl-16176087

ABSTRACT

To construct a novel baculovirus expression system of Spodoptera litura multicapsid nucleopolyhedrovirus, the 5' end and 3' end-flanking fragments of ph gene were amplified from the genome DNA of SpltMNPV, Japan-C3 strain using two pairs of primers synthesized according to SpltMNPV China-G2 strain genome DNA sequence published in GenBank. To obtain the transfer vector pSplt-gfp, the fragment of gfp gene was inserted into this vector between two fragments tandem linked into pUC18. The spli cells were cotransfected with pSplt-gfp and the wild SpltMNPV genome DNA. The recombinant virus containing gfp was selected with the limited dilution method. The fluorescence can be observed in the spli cells and the 3rd instar larvae after 24 and 48 hours by infection of the recombinant virus, respectively. The result showed that the recombinant virus was obtained successfully. It will be helpful to establish Spodoptera litura multicapsid nucleopolyhedrovirus expression system and more effective pesticide for Spodoptera litura.


Subject(s)
Genetic Vectors/genetics , Green Fluorescent Proteins/genetics , Nucleopolyhedroviruses/genetics , Spodoptera/genetics , Spodoptera/virology , Animals , Baculoviridae/genetics , Gene Transfer Techniques , Genetic Vectors/metabolism , Green Fluorescent Proteins/biosynthesis , Larva/genetics , Larva/virology
5.
Guang Pu Xue Yu Guang Pu Fen Xi ; 22(4): 651-4, 2002 Aug.
Article in Chinese | MEDLINE | ID: mdl-12938389

ABSTRACT

This paper studied mechanism of Ce3+, Cd2+, Pb2+ on RNase activity from bovine pancreas. The results showed that the activity of RNase was enhanced under the treatment by Ce3+, Cd2+, Pb2+ at lower concentration (10-60 or 10-30 mumol.L-1), but was inhibited by Ce3+, Cd2+, Pb2+ at higher concentration (40 or 70 mumol.L-1 above), and the inhibition was in the order as Pb2+ > Cd2+ > Ce3+. The equilibrium dialysis demonstrates that RNase may have one Ca(2+)-binding site. The fluorescence titration showed that one molecule of RNase has one binding site for Ce3+, the association constant k for its low-affinity Ce(3+)-binding site is 1.22 x 10(8) L.mol-1. However, it can bind three Cd2+ or Pb2+ and the association causing constant k for its low-affinity Cd2+ or Pb(2+)-binding site is 1.8 x 10(8) L.mol-1, 2.01 x 10(8) L.mol-1, respectively, and caused the conformational changes of RNase.


Subject(s)
Metals, Heavy/chemistry , Ribonuclease, Pancreatic/chemistry , Ribonucleases/chemistry , Animals , Binding Sites , Cadmium/chemistry , Calcium/chemistry , Cattle , Cerium/chemistry , Lead/chemistry
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