Cell‐Surface MMP‐9 Protein Is a Novel Functional Marker to Identify and Separate Proangiogenic Cells from Early Endothelial Progenitor Cells Derived from CD133+ Cells. (22nd February 2016)
- Record Type:
- Journal Article
- Title:
- Cell‐Surface MMP‐9 Protein Is a Novel Functional Marker to Identify and Separate Proangiogenic Cells from Early Endothelial Progenitor Cells Derived from CD133+ Cells. (22nd February 2016)
- Main Title:
- Cell‐Surface MMP‐9 Protein Is a Novel Functional Marker to Identify and Separate Proangiogenic Cells from Early Endothelial Progenitor Cells Derived from CD133+ Cells
- Authors:
- Kanayasu‐Toyoda, Toshie
Tanaka, Takeshi
Kikuchi, Yutaka
Uchida, Eriko
Matsuyama, Akifumi
Yamaguchi, Teruhide - Abstract:
- Abstract: To develop cell therapies for ischemic diseases, endothelial progenitor cells (EPCs) have been expected to play a pivotal role in vascular regeneration. It is desirable to use a molecular marker that is related to the function of the cells. Here, a quantitative polymerase chain reaction array revealed that early EPCs derived from CD133 + cells exhibited significant expression of MMP‐9. Some populations of early EPCs expressed MMP‐9 on the cell surface and others did not. We also attempted to separate the proangiogenic fraction from early EPCs derived from CD133 + cells using a functional cell surface marker, and we then analyzed the MMP‐9 + and MMP‐9 − cell fractions. The MMP‐9 + cells not only revealed higher invasion ability but also produced a high amount of IL‐8. Moreover, the stimulative effect of MMP‐9 + cells on angiogenesis in vitro and in vivo was prohibited by anti‐IL‐8 antibody. These data indicate that MMP‐9 is one of the useful cell surface markers for the separation of angiogenic cells. Our treatment of early EPCs with hyaluronidase caused not only a downregulation of cell‐surface MMP‐9 but also a decrease in invasion ability, indicating that membrane‐bound MMP‐9, which is one of the useful markers for early EPCs, plays an important role in angiogenesis. Stem Cells 2016;34:1251–1262
- Is Part Of:
- Stem cells. Volume 34:Number 5(2016:May)
- Journal:
- Stem cells
- Issue:
- Volume 34:Number 5(2016:May)
- Issue Display:
- Volume 34, Issue 5 (2016)
- Year:
- 2016
- Volume:
- 34
- Issue:
- 5
- Issue Sort Value:
- 2016-0034-0005-0000
- Page Start:
- 1251
- Page End:
- 1262
- Publication Date:
- 2016-02-22
- Subjects:
- Angiogenesis -- Endothelial progenitor cells -- CD133 -- Cell therapy -- Matrix metalloproteinases
Cloning -- Periodicals
Clone cells -- Periodicals
Stem cells -- Periodicals
Cell Differentiation -- Periodicals
Cell Division -- Periodicals
Clone Cells -- Periodicals
Hematopoietic Stem Cells -- Periodicals
Stem Cells -- Periodicals
571.84 - Journal URLs:
- https://academic.oup.com/stmcls ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1002/stem.2300 ↗
- Languages:
- English
- ISSNs:
- 1066-5099
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 8464.133510
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
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