In Vitro and In Vivo Effects of Human Monocytes and their Subsets on New Vessel Formation. (February 2014)
- Record Type:
- Journal Article
- Title:
- In Vitro and In Vivo Effects of Human Monocytes and their Subsets on New Vessel Formation. (February 2014)
- Main Title:
- In Vitro and In Vivo Effects of Human Monocytes and their Subsets on New Vessel Formation
- Authors:
- Czepluch, Frauke S.
Bernhardt, Markus
Kuschicke, Hendrik
Gogiraju, Rajinikanth
Schroeter, Marco R.
Riggert, Joachim
Hasenfuss, Gerd
Schäfer, Katrin - Abstract:
- <abstract abstract-type="main" id="micc12100-abs-0001"> <title>Abstract</title> <sec id="micc12100-sec-0001" sec-type="section"> <title>Objective</title> <p>Human monocytes can be divided into CD16<sup>−</sup> monocytes and CD16<sup>+</sup> monocytes. Studies in mice suggested differential effects of monocyte subsets during new vessel formation.</p> </sec> <sec id="micc12100-sec-0002" sec-type="section"> <title>Methods</title> <p>The functional role of human monocyte subsets in neovascularization processes was investigated. For <italic>in vivo</italic> experiments, nude mice underwent unilateral hindlimb ischemia surgery before being injected with either total monocytes, CD16<sup>−</sup> monocytes or CD16<sup>+</sup> monocytes isolated from healthy individuals.</p> </sec> <sec id="micc12100-sec-0003" sec-type="section"> <title>Results</title> <p> <italic>In vitro</italic>, cytokine array analysis demonstrated that monocytes release numerous angiogenic cytokines, some of which were differentially expressed in monocyte subsets. Sprout length was enhanced in EC spheroids being cultured in conditioned medium obtained from total monocytes and, to a lesser extent, also in supernatants of CD16<sup>−</sup> monocytes. Laser Doppler perfusion imaging up to day 28 after surgery revealed a trend toward improved revascularization in mice treated with monocytes, but no significant differences between monocyte subsets. Histological analyses four weeks after surgery showed an increased<abstract abstract-type="main" id="micc12100-abs-0001"> <title>Abstract</title> <sec id="micc12100-sec-0001" sec-type="section"> <title>Objective</title> <p>Human monocytes can be divided into CD16<sup>−</sup> monocytes and CD16<sup>+</sup> monocytes. Studies in mice suggested differential effects of monocyte subsets during new vessel formation.</p> </sec> <sec id="micc12100-sec-0002" sec-type="section"> <title>Methods</title> <p>The functional role of human monocyte subsets in neovascularization processes was investigated. For <italic>in vivo</italic> experiments, nude mice underwent unilateral hindlimb ischemia surgery before being injected with either total monocytes, CD16<sup>−</sup> monocytes or CD16<sup>+</sup> monocytes isolated from healthy individuals.</p> </sec> <sec id="micc12100-sec-0003" sec-type="section"> <title>Results</title> <p> <italic>In vitro</italic>, cytokine array analysis demonstrated that monocytes release numerous angiogenic cytokines, some of which were differentially expressed in monocyte subsets. Sprout length was enhanced in EC spheroids being cultured in conditioned medium obtained from total monocytes and, to a lesser extent, also in supernatants of CD16<sup>−</sup> monocytes. Laser Doppler perfusion imaging up to day 28 after surgery revealed a trend toward improved revascularization in mice treated with monocytes, but no significant differences between monocyte subsets. Histological analyses four weeks after surgery showed an increased arteriole size in mice having received CD16<sup>+</sup> monocytes, whereas the number of capillaries did not significantly differ between groups.</p> </sec> <sec id="micc12100-sec-0004" sec-type="section"> <title>Conclusions</title> <p>Our findings suggest additive and differential effects of monocyte subsets during neovascularization processes, possibly due to an altered secretion of angiogenic factors and their paracrine capacity to stimulate new vessel formation.</p> </sec> </abstract> … (more)
- Is Part Of:
- Microcirculation. Volume 21:Number 2(2014:Feb.)
- Journal:
- Microcirculation
- Issue:
- Volume 21:Number 2(2014:Feb.)
- Issue Display:
- Volume 21, Issue 2 (2014)
- Year:
- 2014
- Volume:
- 21
- Issue:
- 2
- Issue Sort Value:
- 2014-0021-0002-0000
- Page Start:
- 148
- Page End:
- 158
- Publication Date:
- 2014-02
- Subjects:
- Biological transport -- Periodicals
Microcirculation -- Physiology -- Periodicals
612.135 - Journal URLs:
- http://onlinelibrary.wiley.com/journal/10.1111/(ISSN)1549-8719/issues ↗
http://onlinelibrary.wiley.com/ ↗
http://informahealthcare.com/loi/mic ↗ - DOI:
- 10.1111/micc.12100 ↗
- Languages:
- English
- ISSNs:
- 1073-9688
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 5758.460000
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 3282.xml