scholarly journals Sarcodia suieae Acetyl-xylogalactan Down-regulate RAW264.7 Macrophage Apoptosis Factors Ddit3 and Hyou1 Expression Under Heat Stress

Author(s):  
Kuang-Teng Wang ◽  
Po-Kai Pan ◽  
Tsung-Meng Wu ◽  
Yu-Sheng Wu

We aimed to evaluate the protective effects of acetyl-xylogalactan on the activity of RAW264.7 macrophages against heat stress. To this end, we assessed cell survival, phagocytic activity, in-tracellular Ca2+ level, mitochondria potential exchange, apoptotic assay findings, galactosidase activity and the RNA-seq by NGS and real-time polymerase chain reaction (PCR) expression. In our evaluation of macrophage morphology at 37°C and 41°C, the macrophages showed an oval shape at 41°C , unlike the spindle shape at 37°C. Therefore, 41°C was chosen as the heat stress condition. Subsequently, we designed an experiment to evaluate changes in the RAW264.7 macrophages after acetyl-xylogalactan treatment under heat stress. The survival of RAW264.7 macrophages treated with acetyl-xylogalactan was higher than that of controls that were not treated with acetyl-xylogalactan. Moreover, on the basis of the results of the annexin-V detection assay, the apoptotic activity of macrophages appeared to have reduced after treatment with ac-etyl-xylogalactan. Moreover, treatment with acetyl-xylogalactan resulted in a stronger recovery trend in the intracellular Ca2+ and mitochondrial membrane potential after heat stress. RNA sequencing and real-time polymerase chain reaction (PCR) illustrated that Sarcodia suieae acetyl-xylogalactan could upregulate the expression of the anti-apoptosis Cflar gene and down-regulate the expression of the apoptosis factors Ddit3, and Hyou1 to protect macrophages under heat stress.

Mycologia ◽  
2019 ◽  
Vol 111 (3) ◽  
pp. 493-505 ◽  
Author(s):  
Parivash Shoukouhi ◽  
Carmen Hicks ◽  
Jim G. Menzies ◽  
Zlatko Popovic ◽  
Wen Chen ◽  
...  

2009 ◽  
Vol 65 (3) ◽  
pp. 339-344 ◽  
Author(s):  
Katja A. Koskela ◽  
Pirjo Matero ◽  
Janet M. Blatny ◽  
Else M. Fykse ◽  
Jaran Strand Olsen ◽  
...  

2019 ◽  
Vol 7 (4.14) ◽  
pp. 112
Author(s):  
S S Abd-Gani ◽  
S Mustafa ◽  
M N Mohd Desa ◽  
N F Khairil Mokhtar ◽  
U K Hanapi ◽  
...  

The identification of  lard adulterated in cosmetic cream using TaqMan probe real-time Polymerase Chain Reaction was developed in this research. The laboratory prepared cream was formulated with oil in water (o/w) emulsion with the adulteration of 1%, 3% and 5% of lard (w/w). The total DNA from lard-adulterated cosmetic cream was successfully extracted. The detection assay targeting different gene; universal 18S rRNA and porcine-specific multiple porcine repetitive element (MPRE) which employed with the TaqMan probe. This study targeting 187 bp of amplicons for 18S rRNA while 99 bp of amplicons for Porcine-specific probes. A comparison of quantification cycle (Cq) with prior to percentage of adulteration were detected. Lard-adulterated cream was amplified for 18S rRNA while no detection was detected for Porcine-specific probes. The Cq value obtained might be vary as proposed by the hypothesis depending on the total recovery of extracted DNA from the lard-adulterated cream.  


2006 ◽  
Vol 175 (4S) ◽  
pp. 485-486
Author(s):  
Sabarinath B. Nair ◽  
Christodoulos Pipinikas ◽  
Roger Kirby ◽  
Nick Carter ◽  
Christiane Fenske

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