Thromb Haemost 2012; 107(03): 562-574
DOI: 10.1160/TH11-07-0490
Cardiovascular Biology and Cell Signalling
Schattauer GmbH

Role of early growth response 1 in arteriogenesis: Impact on vascular cell proliferation and leukocyte recruitment in vivo

Judith-Irina Pagel
1   Walter-Brendel-Centre of Experimental Medicine, Ludwig-Maximilians-University, Munich, Germany
,
Tibor Ziegelhoeffer
2   Kerckhoff Clinic, Bad Nauheim, Germany
,
Matthias Heil
3   Max-Planck-Institute for Heart and Lung Research, Bad Nauheim, Germany
,
Silvia Fischer
4   Department of Biochemistry, Justus-Liebig-University, Giessen, Germany
,
Borja Fernández
5   Department of Animal Biology, Faculty of Science, University of Málaga, Málaga, Spain
,
Wolfgang Schaper
3   Max-Planck-Institute for Heart and Lung Research, Bad Nauheim, Germany
,
Klaus T. Preissner
4   Department of Biochemistry, Justus-Liebig-University, Giessen, Germany
,
Elisabeth Deindl
1   Walter-Brendel-Centre of Experimental Medicine, Ludwig-Maximilians-University, Munich, Germany
› Author Affiliations
Financial support: This work was supported in part by grants from the “Förderprogramm für Forschung und Lehre – (FöFoLe)” and the Walter-Brendel-Centre of Experimental Medicine, Medical Faculty, Ludwig-Maximilians-Universität (Munich, Germany), from the Max-Planck-Institute for Heart and Lung Research (Bad Nauheim, Germany), from the Kerckhoff Klinik (Bad Nauheim, Germany), as well as from the von Behring-Röntgen-Foundation (Marburg, Germany) and the “Excellence Cluster Cardio-pulmonary System” (ECCPS) (Giessen. Germany).
Further Information

Publication History

Received: 18 July 2011

Accepted after major revision: 13 February 2011

Publication Date:
22 November 2017 (online)

Summary

Based on previous findings that early growth response 1 (Egr-1) participates in leukocyte recruitment and cell proliferation in vitro, this study was designed to investigate its mode of action during arteriogenesis in vivo. In a model of peripheral arteriogenesis, Egr-1 was significantly upregulated in growing collaterals of wild-type (WT) mice, both on mRNA and protein level. Egr-1−/− mice demonstrated delayed arteriogenesis after femoral artery ligation. They further showed increased levels of monocytes and granulocytes in the circulation, but reduced levels in adductor muscles under baseline conditions. After femoral artery ligation, elevated numbers of macrophages were detected in the perivascular zone of collaterals in Egr-1−/− mice and mRNA of leukocyte recruitment mediators was upregulated. Other Egr family members (Egr-2 to -4) were significantly upregulated only in Egr-1−/− mice, suggesting a mechanism of counterbalancing Egr-1 deficiency. Moreover, splicing factor-1, downregulated in WT mice after femoral artery ligation in the process of increased vascular cell proliferation, was upregulated in Egr-1−/− mice. αSM-actin on the other hand, significantly downregulated in WT mice, showed no differential expression in Egr-1−/− mice. While cell cycle regulator cyclin E and cdc20 were upregulated in Egr-1−/− mice, cyclin D1 expression decreased below the detection limit in collaterals, and the proliferation marker ki67 was not differentially expressed. In conclusion, compensation for deficiency in Egr-1 function in leukocyte recruitment can presumably be mediated by other transcription factors; however, Egr-1 is indispensable for effective vascular cell cycle progression in arteriogenesis.

 
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