Donate Help Contact The AHA Sign In Home
American Heart Association
Circulation Research
Search: search_blue_button Advanced Search
Circulation Research. 2004;95:e56-e64
Published online before print August 26, 2004, doi: 10.1161/01.RES.0000143013.04985.E7
This Article
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow All Versions of this Article:
95/6/e56    most recent
01.RES.0000143013.04985.E7v1
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Right arrow Citation Map
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow Request Permissions
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Khmelewski, E.
Right arrow Articles by Ito, W. D.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Khmelewski, E.
Right arrow Articles by Ito, W. D.
Related Collections
Right arrow Endothelium/vascular type/nitric oxide
Right arrow Other Vascular biology
Right arrow Angiogenesis
Right arrow Animal models of human disease
Right arrow Cell biology/structural biology
(Circulation Research. 2004;95:e56.)
© 2004 American Heart Association, Inc.


UltraRapid Communication

Tissue Resident Cells Play a Dominant Role in Arteriogenesis and Concomitant Macrophage Accumulation

Eugen Khmelewski, Aileen Becker, Thomas Meinertz, Wulf D. Ito

From the Department of Cardiology, University Hospital Hamburg, Hamburg, Germany.

Correspondence to Dr Wulf D. Ito, MD, University Hospital Hamburg, Department of Cardiology, Martinistraße 52, 20246 Hamburg, Germany. E-Mail ito{at}uke.uni-hamburg.de

Collateral growth is characterized by macrophage accumulation, suggesting an important role of circulating cells. To study origin and function of macrophages during arteriogenesis, we related the extent of macrophage accumulation to vascular proliferation and investigated the fate of fluorescently (CMFDA) labeled blood cells that were injected at the time of femoral artery occlusion. The effect of bone marrow depletion via cyclophosphamide before femoral artery occlusion on collateral proliferation and macrophage accumulation was studied, and we looked for the presence of bone marrow-derived stem cells in the vicinity of growing collateral vessels. Finally, we investigated the arteriogenic effect of macrophage activation via MCP-1 in bone marrow-depleted animals. Maximal macrophage accumulation occurred during the first 3 days after femoral artery occlusion and paralleled the extent of vascular proliferation. Fluorescently labeled leukocytes homed to spleen and wound but they were absent in proliferating collateral arteries during maximal macrophage accumulation. Depletion of circulating cells did neither affect macrophage accumulation nor collateral growth. Staining of monocyte-depleted animals for BrdUrd and ED2, {alpha}SMA, or VE-Cadherin demonstrated local proliferation of macrophages and vascular cells, whereas C-Kit, SSEA1, or Thy1-positive bone marrow-derived stem cells were not detectable. Enhancement of macrophage accumulation via MCP-1 was independent of circulating monocytes and promoted arteriogenesis in the absence of direct effects on vascular cells. We propose that the initial phase of vascular growth is characterized by local proliferation of tissue resident precursors rather than by migration of blood born cells. The full text of this article is available online at http://circres.ahajournals.org.


Key Words: arteriogenesis • collateral growth • macrophages • circulating bone marrow-derived cells • resident progenitor cells




This article has been cited by other articles:


Home page
Arterioscler. Thromb. Vasc. Bio.Home page
V. Tchaikovski, G. Fellbrich, and J. Waltenberger
The Molecular Basis of VEGFR-1 Signal Transduction Pathways in Primary Human Monocytes
Arterioscler. Thromb. Vasc. Biol., February 1, 2008; 28(2): 322 - 328.
[Abstract] [Full Text] [PDF]


Home page
J Am Coll CardiolHome page
C. Kupatt, R. Hinkel, M.-L. von Bruhl, T. Pohl, J. Horstkotte, P. Raake, C. El Aouni, E. Thein, S. Dimmeler, O. Feron, et al.
Endothelial Nitric Oxide Synthase Overexpression Provides a Functionally Relevant Angiogenic Switch in Hibernating Pig Myocardium
J. Am. Coll. Cardiol., April 10, 2007; 49(14): 1575 - 1584.
[Abstract] [Full Text] [PDF]


Home page
Am. J. Physiol. Cell Physiol.Home page
N. Landazuri and W. R. Taylor
The stem cell shell game. Focus on "The postnatal rat aorta contains pericyte progenitor cells that form spheroidal colonies in suspension culture"
Am J Physiol Cell Physiol, December 1, 2005; 289(6): C1361 - C1362.
[Full Text] [PDF]


Home page
Cardiovasc ResHome page
A. Pfosser, M. Thalgott, K. Buttner, A. Brouet, O. Feron, P. Boekstegers, and C. Kupatt
Liposomal Hsp90 cDNA induces neovascularization via nitric oxide in chronic ischemia
Cardiovasc Res, February 15, 2005; 65(3): 728 - 736.
[Abstract] [Full Text] [PDF]


Home page
Circ. Res.Home page
I. R. Buschmann and I. E. Hoefer
All Arteriogenesis Is Local? Home Boys Versus the Newcomers
Circ. Res., November 12, 2004; 95(10): e72 - e72.
[Full Text] [PDF]