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Articles in PresS, published online ahead of print October 3, 2002
Am J Physiol Heart Circ Physiol, 10.1152/ajpheart.01098.2001
Submitted on December 14, 2001
Accepted on August 5, 2002
1 Department of Experimental Cardiology, Max-Planck-Institute for Physiological and Clinical Research, Bad Nauheim, Germany
2 Department of Molecular Cellbiology, Max-Planck-Institute for Physiological and Clinical Research, Bad Nauheim, Germany
* To whom correspondence should be addressed. E-mail: m.heil{at}kerckhoff.mpg.de.
Arteriogenesis has been associated with the presence of monocytes/macrophages within the collateral vessel wall. Here we tested the hypothesis that arteriogenesis is functionally linked to the concentration of circulating blood monocytes. Monocyte concentrations in peripheral blood were manipulated by single injections of the antimetabolite 5-fluorouracil (5-FU) resulting in a marked rebound effect in NZW-rabbits. Collateral artery growth was assessed by a model of acute femoral artery ligation. Seven days after ligation collateral conductance and number of visible collateral arteries were increased in the rebound group. This increase was accompanied by an increased monocyte accumulation as demonstrated by immunohistology in the thigh three days after surgery. In a second animal model, namely in 129S2/SvHsd mice, 5-FU-treatment caused a remarkable decrease in blood monocyte numbers at day four followed by a rebound effect at day 12. Foot blood flow, assessed by Laser-Doppler-Imaging before and at various time points after surgery increased from day seven on in mice of the rebound group. In contrast, ligation during the phase of monocyte depletion resulted in a reduction of blood flow reconstitution. This inhibition could be reversed by an injection of isolated monocytes. In conclusion, we have demonstrated a functional link between the monocyte concentration in the peripheral blood and the enhancement of arteriogenesis.
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