Placenta Growth Factor and Vascular Endothelial Growth Factor A Have Differential, Cell‐Type Specific Patterns of Expression in Vascular Cells. (July 2014)
- Record Type:
- Journal Article
- Title:
- Placenta Growth Factor and Vascular Endothelial Growth Factor A Have Differential, Cell‐Type Specific Patterns of Expression in Vascular Cells. (July 2014)
- Main Title:
- Placenta Growth Factor and Vascular Endothelial Growth Factor A Have Differential, Cell‐Type Specific Patterns of Expression in Vascular Cells
- Authors:
- Xiang, Lingjin
Varshney, Rohan
Rashdan, Nabil A.
Shaw, Jennifer H.
Lloyd, Pamela G. - Abstract:
- <abstract abstract-type="main" id="micc12113-abs-0001"> <title>Abstract</title> <sec id="micc12113-sec-0001" sec-type="section"> <title>Objective</title> <p>PLGF, a VEGF‐A related protein, mediates collateral enlargement via monocytes but plays little role in capillary proliferation. In contrast, VEGF‐A mediates both collateral enlargement and capillary proliferation. PLGF has been less thoroughly studied than VEGF‐A, and questions remain regarding its regulation and function. Therefore, our goal was to characterize the expression of PLGF by vascular cells. We hypothesized that vascular SMC would express more PLGF than EC, since VEGF‐A is primarily expressed by non‐EC.</p> </sec> <sec id="micc12113-sec-0002" sec-type="section"> <title>Methods</title> <p>We compared PLGF and VEGF‐A across eight EC and SMC lines, then knocked down PLGF and evaluated cell function. We also assessed the effect of hypoxia on PLGF expression and promoter activity.</p> </sec> <sec id="micc12113-sec-0003" sec-type="section"> <title>Results</title> <p>PLGF was most highly expressed in EC, whereas VEGF‐A was most highly expressed in SMC. PLGF knockdown did not affect EC number, migration, or tube formation, but reduced monocyte migration toward EC. Monocyte migration was rescued by exogenous PLGF. Hypoxia increased PLGF protein without activating PLGF gene transcription.</p> </sec> <sec id="micc12113-sec-0004" sec-type="section"> <title>Conclusions</title> <p>PLGF and VEGF‐A have distinct patterns of<abstract abstract-type="main" id="micc12113-abs-0001"> <title>Abstract</title> <sec id="micc12113-sec-0001" sec-type="section"> <title>Objective</title> <p>PLGF, a VEGF‐A related protein, mediates collateral enlargement via monocytes but plays little role in capillary proliferation. In contrast, VEGF‐A mediates both collateral enlargement and capillary proliferation. PLGF has been less thoroughly studied than VEGF‐A, and questions remain regarding its regulation and function. Therefore, our goal was to characterize the expression of PLGF by vascular cells. We hypothesized that vascular SMC would express more PLGF than EC, since VEGF‐A is primarily expressed by non‐EC.</p> </sec> <sec id="micc12113-sec-0002" sec-type="section"> <title>Methods</title> <p>We compared PLGF and VEGF‐A across eight EC and SMC lines, then knocked down PLGF and evaluated cell function. We also assessed the effect of hypoxia on PLGF expression and promoter activity.</p> </sec> <sec id="micc12113-sec-0003" sec-type="section"> <title>Results</title> <p>PLGF was most highly expressed in EC, whereas VEGF‐A was most highly expressed in SMC. PLGF knockdown did not affect EC number, migration, or tube formation, but reduced monocyte migration toward EC. Monocyte migration was rescued by exogenous PLGF. Hypoxia increased PLGF protein without activating PLGF gene transcription.</p> </sec> <sec id="micc12113-sec-0004" sec-type="section"> <title>Conclusions</title> <p>PLGF and VEGF‐A have distinct patterns of expression in vascular cells. EC derived PLGF may function primarily in communication between EC and circulating cells. Hypoxia increases EC PLGF expression posttranscriptionally.</p> </sec> </abstract> … (more)
- Is Part Of:
- Microcirculation. Volume 21:Number 5(2014:Jul.)
- Journal:
- Microcirculation
- Issue:
- Volume 21:Number 5(2014:Jul.)
- Issue Display:
- Volume 21, Issue 5 (2014)
- Year:
- 2014
- Volume:
- 21
- Issue:
- 5
- Issue Sort Value:
- 2014-0021-0005-0000
- Page Start:
- 368
- Page End:
- 379
- Publication Date:
- 2014-07
- 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.12113 ↗
- 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:
- 4211.xml