2015
DOI: 10.1016/j.carbpol.2015.04.070
|View full text |Cite
|
Sign up to set email alerts
|

Activation of RAW 264.7 cells by a polysaccharide isolated from Antarctic bacterium Pseudoaltermonas sp. S-5

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
2
2
1

Citation Types

3
20
0

Year Published

2016
2016
2024
2024

Publication Types

Select...
9

Relationship

0
9

Authors

Journals

citations
Cited by 41 publications
(23 citation statements)
references
References 30 publications
3
20
0
Order By: Relevance
“…The morphology of macrophages changes with the cell activity, function, and environment. When stimulated with LPS or other signaling factors, the morphology of RAW264.7 cells was altered [43]. In this study, morphological changes of RAW264.7 cells treated with NJP or LPS were investigated under an inverted microscope.…”
Section: Resultsmentioning
confidence: 99%
“…The morphology of macrophages changes with the cell activity, function, and environment. When stimulated with LPS or other signaling factors, the morphology of RAW264.7 cells was altered [43]. In this study, morphological changes of RAW264.7 cells treated with NJP or LPS were investigated under an inverted microscope.…”
Section: Resultsmentioning
confidence: 99%
“…TNFa and IL-6 transcription have been documented to be inuenced by both MAPK and NF-kB pathway. 22 The transcription factor NF-kB plays a central role in the regulation of many immune and inammatory responses. 23 NF-kB forms an inactive cytoplasmic complex together with its inhibitor (IkBa) in unstimulated cells.…”
Section: Discussionmentioning
confidence: 99%
“…After removing the cell supernatants, an MTT assay was used to determine cell viability (Li et al, 2015;Zhang et al, 2016). After removing the cell supernatants, an MTT assay was used to determine cell viability (Li et al, 2015;Zhang et al, 2016).…”
Section: Cell Culturementioning
confidence: 99%
“…Cell viability assay RAW 264.7 cells (1 9 10 6 cells mL À1 ) were incubated for 24 h and treated with 62.5, 125, 250, 500 and 1000 lg mL À1 DAP for another 24 h. An equal volume of medium was used as controls. After removing the cell supernatants, an MTT assay was used to determine cell viability (Li et al, 2015;Zhang et al, 2016).…”
Section: Cell Culturementioning
confidence: 99%