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典型文献
Toxoplasma gondii infection induces cell apoptosis via multiple pathways revealed by transcriptome analysis
文献摘要:
Toxoplasma gondii is a worldwide parasite that can infect almost all kinds of mammals and cause fatal toxoplasmosis in immunocompromised patients. Apoptosis is one of the principal strategies of host cells to clear pathogens and maintain organismal homeostasis, but the mechanism of cell apoptosis induced by T. gondii remains obscure. To explore the apoptosis influenced by T. gondii, Vero cells infected or uninfected with the parasite were subjected to apoptosis detection and subsequent dual RNA sequencing (RNA-seq). Using high-throughput Illumina sequencing and bioinformatics analysis, we found that pro-apoptosis genes such as DNA damage-inducible transcript 3 (DDIT3), growth arrest and DNA damage-inducible α (GADD45A), caspase-3 (CASP3), and high-temperature requirement protease A2 (HtrA2) were upregulated, and anti-apoptosis genes such as poly(adenosine diphosphate (ADP)-ribose) polymerase family member 3 (PARP3), B-cell lymphoma 2 (Bcl-2), and baculoviral inhibitor of apoptosis protein (IAP) repeat containing 5 (BIRC5) were downregulated. Besides, tumor necrosis factor (TNF) receptor-associated factor 1 (TRAF1), TRAF2, TNF receptor superfamily member 10b (TNFRSF10b), disabled homolog 2 (DAB2)-interacting protein (DAB2IP), and inositol 1,4,5-trisphosphate receptor type 3 (ITPR3) were enriched in the upstream of TNF, TNF-related apoptosis-inducing ligand (TRAIL), and endoplasmic reticulum (ER) stress pathways, and TRAIL-receptor 2 (TRAIL-R2) was regarded as an important membrane receptor influenced by T. gondii that had not been previously considered. In conclusion, the T. gondii RH strain could promote and mediate apoptosis through multiple pathways mentioned above in Vero cells. Our findings improve the understanding of the T. gondii infection process through providing new insights into the related cellular apoptosis mechanisms.
文献关键词:
作者姓名:
Kaige DU;Fei LU;Chengzuo XIE;Haojie DING;Yu SHEN;Yafan GAO;Shaohong LU;Xunhui ZHUO
作者机构:
School of Basic Medical Sciences and Forensic Medicine,Hangzhou Medical College,Hangzhou 310053,China;Shandong Center for Disease Control and Prevention,Jinan 250021,China
引用格式:
[1]Kaige DU;Fei LU;Chengzuo XIE;Haojie DING;Yu SHEN;Yafan GAO;Shaohong LU;Xunhui ZHUO-.Toxoplasma gondii infection induces cell apoptosis via multiple pathways revealed by transcriptome analysis)[J].浙江大学学报(英文版)(B辑:生物医学和生物技术),2022(04):315-327
A类:
PARP3,TRAF1,TNFRSF10b,DAB2IP,ITPR3
B类:
Toxoplasma,gondii,infection,induces,apoptosis,via,multiple,pathways,revealed,by,transcriptome,analysis,worldwide,parasite,that,can,almost,all,kinds,mammals,cause,fatal,toxoplasmosis,immunocompromised,patients,Apoptosis,principal,strategies,host,cells,clear,pathogens,maintain,organismal,homeostasis,but,induced,remains,obscure,explore,influenced,Vero,uninfected,were,subjected,detection,subsequent,dual,sequencing,Using,high,throughput,Illumina,bioinformatics,found,genes,such,damage,inducible,DDIT3,growth,arrest,GADD45A,caspase,CASP3,temperature,requirement,protease,HtrA2,upregulated,anti,adenosine,diphosphate,ADP,ribose,polymerase,member,lymphoma,Bcl,baculoviral,inhibitor,protein,IAP,repeat,containing,BIRC5,downregulated,Besides,tumor,necrosis,receptor,associated,TRAF2,superfamily,disabled,homolog,interacting,inositol,trisphosphate,type,enriched,upstream,related,inducing,ligand,TRAIL,endoplasmic,reticulum,ER,stress,was,regarded,important,membrane,had,not,been,previously,considered,In,conclusion,RH,strain,could,promote,mediate,mentioned,above,Our,findings,improve,understanding,process,providing,new,insights,into,cellular,mechanisms
AB值:
0.584973
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