Abstract
To investigate the role of TIE-2/angiopoietins (Angs) in postnatal hematopoiesis, we cultured bone marrow cells in the presence of Ang-1 and -2 with or without VEGF. While either Ang-1 or Ang-2 alone had hematopoietic effects on unseparated bone marrow cells and no effect on proliferation of endothelial cells, both enhanced the growth of endothelial cells and hematopoietic progenitor cells in the presence of VEGF. FACS analysis showed that Lin-TIE-2+Flk-1+ cells cocultured with OP9 stromal cells gave rise to endothelial and hematopoietic cells in the presence of VEGF and Ang-1. Ang-1 promoted the adhesion of sorted primary Lin-TIE-2+ cells to fibronectin, and this adhesion enhanced proliferation of hematopoietic progenitor cells synergistically with stem cell factor (SCF). Our findings suggest that TIE-2/angiopoietins may act as critical regulators of proliferation of hematopoietic progenitors and endothelial cells in a synergistic manner.
| Original language | English |
|---|---|
| Pages (from-to) | 133-138 |
| Number of pages | 6 |
| Journal | Biochemical and Biophysical Research Communications |
| Volume | 264 |
| Issue number | 1 |
| DOIs | |
| Publication status | Published - 1999 Oct 14 |
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Keywords
- Cell adhesion and proliferation
- Endothelial cells
- Hematopoietic progenitors
ASJC Scopus subject areas
- Biochemistry
- Biophysics
- Molecular Biology
Cite this
In vitro effects of angiopoietins and VEGF on hematopoietic and endothelial cells. / Huang, Xu Ling; Takakura, Nobuyuki; Suda, Toshio.
In: Biochemical and Biophysical Research Communications, Vol. 264, No. 1, 14.10.1999, p. 133-138.Research output: Contribution to journal › Article
}
TY - JOUR
T1 - In vitro effects of angiopoietins and VEGF on hematopoietic and endothelial cells
AU - Huang, Xu Ling
AU - Takakura, Nobuyuki
AU - Suda, Toshio
PY - 1999/10/14
Y1 - 1999/10/14
N2 - To investigate the role of TIE-2/angiopoietins (Angs) in postnatal hematopoiesis, we cultured bone marrow cells in the presence of Ang-1 and -2 with or without VEGF. While either Ang-1 or Ang-2 alone had hematopoietic effects on unseparated bone marrow cells and no effect on proliferation of endothelial cells, both enhanced the growth of endothelial cells and hematopoietic progenitor cells in the presence of VEGF. FACS analysis showed that Lin-TIE-2+Flk-1+ cells cocultured with OP9 stromal cells gave rise to endothelial and hematopoietic cells in the presence of VEGF and Ang-1. Ang-1 promoted the adhesion of sorted primary Lin-TIE-2+ cells to fibronectin, and this adhesion enhanced proliferation of hematopoietic progenitor cells synergistically with stem cell factor (SCF). Our findings suggest that TIE-2/angiopoietins may act as critical regulators of proliferation of hematopoietic progenitors and endothelial cells in a synergistic manner.
AB - To investigate the role of TIE-2/angiopoietins (Angs) in postnatal hematopoiesis, we cultured bone marrow cells in the presence of Ang-1 and -2 with or without VEGF. While either Ang-1 or Ang-2 alone had hematopoietic effects on unseparated bone marrow cells and no effect on proliferation of endothelial cells, both enhanced the growth of endothelial cells and hematopoietic progenitor cells in the presence of VEGF. FACS analysis showed that Lin-TIE-2+Flk-1+ cells cocultured with OP9 stromal cells gave rise to endothelial and hematopoietic cells in the presence of VEGF and Ang-1. Ang-1 promoted the adhesion of sorted primary Lin-TIE-2+ cells to fibronectin, and this adhesion enhanced proliferation of hematopoietic progenitor cells synergistically with stem cell factor (SCF). Our findings suggest that TIE-2/angiopoietins may act as critical regulators of proliferation of hematopoietic progenitors and endothelial cells in a synergistic manner.
KW - Cell adhesion and proliferation
KW - Endothelial cells
KW - Hematopoietic progenitors
UR - http://www.scopus.com/inward/record.url?scp=0033554621&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=0033554621&partnerID=8YFLogxK
U2 - 10.1006/bbrc.1999.1472
DO - 10.1006/bbrc.1999.1472
M3 - Article
VL - 264
SP - 133
EP - 138
JO - Biochemical and Biophysical Research Communications
JF - Biochemical and Biophysical Research Communications
SN - 0006-291X
IS - 1
ER -