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Arteriosclerosis, Thrombosis, and Vascular Biology
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Arteriosclerosis, Thrombosis, and Vascular Biology. 2007;27:263-265
doi: 10.1161/01.ATV.0000256727.34148.e2
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(Arteriosclerosis, Thrombosis, and Vascular Biology. 2007;27:263.)
© 2007 American Heart Association, Inc.


Editorials

CXCR4, a Key Modulator of Vascular Progenitor Cells

Julie Sainz; Masataka Sata

From the Departments of Cardiovascular Medicine (J.S., M.S.) and Advanced Clinical Science and Therapeutics (M.S.), University of Tokyo, Japan.

Correspondence to Dr Masataka Sata, Department of Cardiovascular Medicine, University of Tokyo Graduate School of Medicine, 7-3-1 Hongo, Bunkyo-ku, Tokyo 113-8655, Japan. E-mail msata-circ@umin.net


An extract of the first 250 words of the full text is provided, because this article has no abstract.
 

A growing body of evidence suggests that circulating progenitors participate in vascular healing and remodeling under physiological and pathological conditions (Figure).1–3 It is believed that the majority of vascular progenitor cells originate from the bone marrow. Stem cells within the bone marrow usually exist in a quiescent state. Specific signals stimulate the stem cells to differentiate and move to systemic circulation (Mobilization). Progenitors are recruited and stay at the site of vascular repair or neovascularization (Homing), where they differentiate into endothelial-like cells or smooth muscle–like cells (Differentiation) and proliferate (Proliferation). The molecular processes leading to their mobilization from the bone marrow and homing to the sites of vascular remodeling or neovascularization are not fully understood.4,5 In the current issue of Arteriosclerosis, Thrombosis, and Vascular Biology, two articles6,7 provide new insights into the essential role of CXCR4, the receptor for stromal cell–derived factor-1 (SDF-1) for the mobilization and the recruitment of bone marrow (BM)-derived cells. CXCR4 is notably expressed on hematopoietic stem cells and has previously been shown to play a key role in their homing and mobilization.8 Activation of this G protein–coupled 7-transmembrane receptor induces adhesion molecules on the hematopoietic progenitor/stem cell surface thereby enhancing their homing capacities9 and regulating their proliferation.10


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Contribution of bone marrow–derived cells to neointima formation and angiogenesis. On severe vascular injury, bone marrow–derived cells are recruited to the injured artery and contribute to neointima formation by differentiating into smooth muscle–like cells (left). When new vessels grow, endothelial progenitor cells (EPCs) are mobilized . . . [Full Text of this Article]


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Yuji Shiba, Masafumi Takahashi, Toru Yoshioka, Noriyuki Yajima, Hajime Morimoto, Atsushi Izawa, Hirohiko Ise, Kiyohiko Hatake, Kazuo Motoyoshi, and Uichi Ikeda
Arterioscler Thromb Vasc Biol 2007 27: 283-289. [Abstract] [Full Text] [PDF]

Sphingosine-1-Phosphate Stimulates the Functional Capacity of Progenitor Cells by Activation of the CXCR4-Dependent Signaling Pathway via the S1P3 Receptor
Dirk H. Walter, Ulrich Rochwalsky, Johannes Reinhold, Florian Seeger, Alexandra Aicher, Carmen Urbich, Ioakim Spyridopoulos, Jerold Chun, Volker Brinkmann, Petra Keul, Bodo Levkau, Andreas M. Zeiher, Stefanie Dimmeler, and Judith Haendeler
Arterioscler Thromb Vasc Biol 2007 27: 275-282. [Abstract] [Full Text] [PDF]



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