The JAK/STAT3 signalling pathway regulated angiogenesis in an endothelial cell/adipose‐derived stromal cell co‐culture, 3D gel model. (25th September 2016)
- Record Type:
- Journal Article
- Title:
- The JAK/STAT3 signalling pathway regulated angiogenesis in an endothelial cell/adipose‐derived stromal cell co‐culture, 3D gel model. (25th September 2016)
- Main Title:
- The JAK/STAT3 signalling pathway regulated angiogenesis in an endothelial cell/adipose‐derived stromal cell co‐culture, 3D gel model
- Authors:
- Xue, Changyue
Xie, Jiamin
Zhao, Dan
Lin, Shiyu
Zhou, Tengfei
Shi, Sirong
Shao, Xiaoru
Lin, Yunfeng
Zhu, Bofeng
Cai, Xiaoxiao - Abstract:
- Abstract: Objectives: The aim of the study was to investigate the role of the JAK/STAT3 signalling pathway in angiogenesis. Materials and methods: The model established in vitro, involved a 3D collagen gel being implanted with endothelial cells (ECs) from red fluorescent protein‐labelled mice, and adipose‐derived stromal cells (ASCs) from green fluorescent protein‐labelled mice. Phenomena of angiogenesis, after treatment by the inhibitor and the activator of JAK/STAT3 pathway respectively, were observed using confocal laser scanning microscopy. Transwell co‐culture of ECs and ASCs was used to elucidate mechanisms. Results: Stattic, inhibitor of JAK/STAT3 pathway, attenuated angiogenesis in the model. In contrast, angiogenesis was promoted after treatment of Olanzapine, an activator. We found that protein levels of VEGFA and cyclin D1 were regulated by the JAK/STAT3 pathway, and flow cytometry further confirmed variations in cell cycle parameters of ECs and ASCs. Genes VEGFA/B, VEGFR2, MMP‐2, MMP‐9, IGF‐1 and b‐FGF were down‐regulated by Stattic in ECs, while Olanzapine significantly up‐regulated mRNA levels of these genes. As for ASCs, genes VEGFA, MMP‐2, MMP‐9, IGF‐1 and b‐FGF were modulated by the JAK/STAT3 pathway. Conclusions: Angiogenesis in the 3D collagen gel was regulated by the JAK/STAT3 pathway which involved changes in vessel length, vessel diameter and sprout number. The underlying mechanism was that the JAK/STAT3 signalling pathway regulated angiogenesis byAbstract: Objectives: The aim of the study was to investigate the role of the JAK/STAT3 signalling pathway in angiogenesis. Materials and methods: The model established in vitro, involved a 3D collagen gel being implanted with endothelial cells (ECs) from red fluorescent protein‐labelled mice, and adipose‐derived stromal cells (ASCs) from green fluorescent protein‐labelled mice. Phenomena of angiogenesis, after treatment by the inhibitor and the activator of JAK/STAT3 pathway respectively, were observed using confocal laser scanning microscopy. Transwell co‐culture of ECs and ASCs was used to elucidate mechanisms. Results: Stattic, inhibitor of JAK/STAT3 pathway, attenuated angiogenesis in the model. In contrast, angiogenesis was promoted after treatment of Olanzapine, an activator. We found that protein levels of VEGFA and cyclin D1 were regulated by the JAK/STAT3 pathway, and flow cytometry further confirmed variations in cell cycle parameters of ECs and ASCs. Genes VEGFA/B, VEGFR2, MMP‐2, MMP‐9, IGF‐1 and b‐FGF were down‐regulated by Stattic in ECs, while Olanzapine significantly up‐regulated mRNA levels of these genes. As for ASCs, genes VEGFA, MMP‐2, MMP‐9, IGF‐1 and b‐FGF were modulated by the JAK/STAT3 pathway. Conclusions: Angiogenesis in the 3D collagen gel was regulated by the JAK/STAT3 pathway which involved changes in vessel length, vessel diameter and sprout number. The underlying mechanism was that the JAK/STAT3 signalling pathway regulated angiogenesis by modulation of numbers of angiogenesis‐related growth factors and by direct regulation of cell cycle. … (more)
- Is Part Of:
- Cell proliferation. Volume 50:Number 1(2017:Feb.)
- Journal:
- Cell proliferation
- Issue:
- Volume 50:Number 1(2017:Feb.)
- Issue Display:
- Volume 50, Issue 1 (2017)
- Year:
- 2017
- Volume:
- 50
- Issue:
- 1
- Issue Sort Value:
- 2017-0050-0001-0000
- Page Start:
- n/a
- Page End:
- n/a
- Publication Date:
- 2016-09-25
- Subjects:
- Cell proliferation -- Periodicals
571.84 - Journal URLs:
- http://onlinelibrary.wiley.com/journal/10.1111/(ISSN)1365-2184 ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1111/cpr.12307 ↗
- Languages:
- English
- ISSNs:
- 0960-7722
- Deposit Type:
- Legaldeposit
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- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 3097.854000
British Library DSC - BLDSS-3PM
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- 2116.xml