این سایت در حال حاضر پشتیبانی نمی شود و امکان دارد داده های نشریات بروز نباشند
صفحه اصلی
درباره پایگاه
فهرست سامانه ها
الزامات سامانه ها
فهرست سازمانی
تماس با ما
JCR 2016
جستجوی مقالات
پنجشنبه 27 آذر 1404
Cell Journal
، جلد ۲۲، شماره ۳، صفحات ۳۲۵-۳۳۳
عنوان فارسی
چکیده فارسی مقاله
کلیدواژههای فارسی مقاله
عنوان انگلیسی
PolyI:C Upregulated CCR5 and Promoted THP-1-Derived Macrophage Chemotaxis via TLR3/JMJD1A Signalling
چکیده انگلیسی مقاله
Objective
This study aimed to evaluate the specific roles of polyinosinic:polycytidylic acid (polyI:C) in macrophage chemotaxis and reveal the potential regulatory mechanisms related to chemokine receptor 5 (CCR5).
Materials and Methods
In this experimental study, THP-1-derived macrophages (THP1-Mφs) induced from THP- 1 monocytes were treated with 25 μg/mL polyI:C. Toll-like receptor 3 (TLR3), Jumonji domain-containing protein (JMJD)1A, and JMJD1C small interfering RNA (siRNAs) were transfected into THP1-Mφs. Quantitative real-time reverse transcriptase polymerase chain reaction (qRT-PCR) was used to detect the expression levels of TLR3, CCR5, 23 Jumonji C domain-containing histone demethylase family members, JMJD1A, and JMJD1C in THP1-Mφs with different siRNAs transfections. Western blot was performed to detect JMJD1A, JMJD1C, H3K9me2, and H3K9me3 expressions. A transwell migration assay was conducted to detect THP1-Mφ chemotaxis toward chemokine ligand 3 (CCL3). A chromatin immunoprecipitation (ChIP) assay was performed to detect H3K9me2-CCR5 complexes in THP1- Mφs.
Results
PolyI:C significantly upregulated CCR5 in THP1-Mφs and promoted chemotaxis toward CCL3 (P < 0.05); these effects were significantly inhibited by TLR3 siRNA (P < 0.01). JMJD1A and JMJD1C expression was significantly upregulated in polyI:C-stimulated THP1-Mφs, while only JMJD1A siRNA decreased CCR5 expression (P < 0.05). JMJD1A siRNA significantly increased H3K9me2 expression in THP1-Mφs but not in polyI:C-stimulated THP1-Mφs. The ChIP result revealed that polyI:C significantly downregulated H3K9me2 in the promoter region of CCR5 in THP1- Mφs.
Conclusion
PolyI:C can enhance THP1-Mφ chemotaxis toward CCL3 regulated by TLR3/JMJD1A signalling and activate CCR5 expression by reducing H3K9me2 in the promoter region of CCR5.
کلیدواژههای انگلیسی مقاله
Chemokine Receptor 5, Chemotaxis, macrophages, Polyinosinicpolycytidylic Acid
نویسندگان مقاله
Xiaoxiao Yu |
.Department of Paediatrics, Qilu Hospital of Shandong University, Jinan, Shandong, China
Huayang Wang |
. Department of Clinical Laboratory, Qilu Hospital of Shandong University, Jinan, Shandong, China
Hongjia Shao |
.Department of Paediatrics, Qilu Hospital of Shandong University, Jinan, Shandong, China
Cuijuan Zhang |
.Department of Pathology, Qilu Hospital of Shandong University, Jinan, Shandong, China
Xiuli Ju |
.Department of Paediatrics, Qilu Hospital of Shandong University, Jinan, Shandong, China
Jie Yang |
.Department of Paediatrics, Qilu Hospital of Shandong University, Jinan, Shandong, China
نشانی اینترنتی
https://www.celljournal.org/article_250654_61f069e8b1922521ed28fbdd30de000f.pdf
فایل مقاله
فایلی برای مقاله ذخیره نشده است
کد مقاله (doi)
زبان مقاله منتشر شده
en
موضوعات مقاله منتشر شده
نوع مقاله منتشر شده
برگشت به:
صفحه اول پایگاه
|
نسخه مرتبط
|
نشریه مرتبط
|
فهرست نشریات