2020
DOI: 10.1111/jcmm.15220
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Interleukin‐1β augments the angiogenesis of endothelial progenitor cells in an NF‐κB/CXCR7‐dependent manner

Abstract: This is an open access article under the terms of the Creative Commons Attribution License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.

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Cited by 18 publications
(17 citation statements)
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“…NF-κB is a well-known transcription factor associated with inflammation and bone resorption. 51 Many studies reported orthodontic mechanical stress could trigger the NF-κB pathway activation, which mediated the expression of pro-inflammatory genes such as TNF-α and IL-6, as proved in our histological findings. 52 Therefore, inhibition of NF-κB activation is an important process in increasing tooth anchorage.…”
Section: Discussionssupporting
confidence: 78%
“…NF-κB is a well-known transcription factor associated with inflammation and bone resorption. 51 Many studies reported orthodontic mechanical stress could trigger the NF-κB pathway activation, which mediated the expression of pro-inflammatory genes such as TNF-α and IL-6, as proved in our histological findings. 52 Therefore, inhibition of NF-κB activation is an important process in increasing tooth anchorage.…”
Section: Discussionssupporting
confidence: 78%
“…Angiogenesis is one of the characteristics of malignant glioma, contributing to tumor proliferation and unfavorable prognosis [34]. The activation of the in ammatory response and IL6/JAK-STAT3 signaling pathway has been shown to play important roles in promoting this process [35,36]. In the present study, the multiple functional analysis of HOXB5-corelated genes revealed a signi cant association between HOXB5 and the regulation of angiogenesis, in ammatory response, and the IL6/JAK-STAT3 pathway.…”
Section: Discussionmentioning
confidence: 48%
“…The research ethics committee of the First Affiliated Hospital of Wenzhou Medical University approved all protocols, and informed consent was obtained from the parents of the newborns. EPCs were isolated as described in previous studies 17‐19 . Briefly, cord blood was diluted 1:1 with Hanks' balanced salt solution (HBSS; Invitrogen), carefully overlaid onto an equivalent volume of Histopaque 1077 (Sigma) and centrifuged at 400 g for 30 minutes at room temperature.…”
Section: Methodsmentioning
confidence: 99%
“…EPCs were isolated as described in previous studies. [17][18][19] Briefly, cord blood was diluted 1:1 with Hanks' balanced salt solution (HBSS; Invitrogen), carefully overlaid onto an equivalent volume of Histopaque 1077 (Sigma) and centrifuged at 400 g for 30 minutes at room temperature. Thereafter, the buffy coat was collected and washed with HBSS twice, and cell aggregate was resuspended in EGM-2 (Lonza) supplemented with 2% FBS (Sigma) and plated onto 6-well plates that were pre-coated with human fibronectin (2 μg/ cm 2 ; BD Biosciences).…”
Section: Human Umbilical Cord Blood Epcs Isolation and Identificationmentioning
confidence: 99%
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