Syndecan-4 Enhances Therapeutic Angiogenesis after Hind Limb Ischemia in Mice with Type 2 Diabetes

被引:27
作者
Das, Subhamoy [1 ]
Monteforte, Anthony J. [1 ]
Singh, Gunjan [1 ]
Majid, Marjan [1 ]
Sherman, Michael B. [2 ]
Dunn, Andrew K. [1 ]
Baker, Aaron B. [1 ,3 ,4 ,5 ]
机构
[1] Univ Texas Austin, Dept Biomed Engn, Austin, TX USA
[2] Univ Texas Med Branch, Sealy Ctr Struct Biol & Mol Biophys, Galveston, TX 77555 USA
[3] Univ Texas Austin, Inst Cellular & Mol Biol, Austin, TX 78712 USA
[4] Univ Texas Austin, Inst Computat Engn & Sci, Austin, TX 78712 USA
[5] Univ Texas Austin, Inst Biomat Drug Delivery & Regenerat Med, Austin, TX 78712 USA
关键词
PERIPHERAL ARTERIAL-DISEASE; FIBROBLAST GROWTH FACTOR-2; INTERMITTENT CLAUDICATION; DOUBLE-BLIND; TRIAL; PLACEBO;
D O I
10.1002/adhm.201500993
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
Delivering syndecan-4 with FGF-2 improves the effectiveness of FGF-2 therapy for ischemia in the diabetic disease state. The syndecan-4 proteoliposomes significantly enhance in vitro tubule formation as well as blood perfusion and vessel density in the ischemic hind limbs of diseased ob/ob mice. Syndecan-4 therapy also induces a marked immunomodulation in the tissues, increasing the polarization of macrophages toward the M2 phenotype. © 2016 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.
引用
收藏
页码:1008 / 1013
页数:6
相关论文
共 20 条
[1]   Economic Costs of Diabetes in the U.S. in 2012 [J].
Yang W. ;
Dall T.M. ;
Halder P. ;
Gallo P. ;
Kowal S.L. ;
Hogan P.F. ;
Petersen M. .
DIABETES CARE, 2013, 36 (04) :1033-1046
[2]  
Bruhn-Olszewska B, 2012, ACTA BIOCHIM POL, V59, P507
[3]   Overcoming disease-induced growth factor resistance in therapeutic angiogenesis using recombinant co-receptors delivered by a liposomal system [J].
Das, Subhamoy ;
Singh, Gunjan ;
Baker, Aaron B. .
BIOMATERIALS, 2014, 35 (01) :196-205
[4]   Syndecan-4 signaling at a glance [J].
Elfenbein, Arye ;
Simons, Michael .
JOURNAL OF CELL SCIENCE, 2013, 126 (17) :3799-3804
[5]   Syndecan-4 proteoliposomes enhance fibroblast growth factor-2 (FGF-2)-induced proliferation, migration, and neovascularization of ischemic muscle [J].
Jang, Eugene ;
Albadawi, Hassan ;
Watkins, Michael T. ;
Edelman, Elazer R. ;
Baker, Aaron B. .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2012, 109 (05) :1679-1684
[6]   Inflammation and wound healing: the role of the macrophage [J].
Koh, Timothy J. ;
DiPietro, Luisa Ann .
EXPERT REVIEWS IN MOLECULAR MEDICINE, 2011, 13 :e23
[7]   Treatment with intramuscular vascular endothelial growth factor gene compared with placebo for patients with diabetes mellitus and critical limb ischemia: A double-blind randomized trial [J].
Kusumanto, Y. H. ;
Van Weel, V. ;
Mulder, N. H. ;
Smit, A. J. ;
Van den Dungen, J. J. A. M. ;
Hooymans, J. M. M. ;
Sluiter, W. J. ;
Tio, R. A. ;
Quax, P. H. A. ;
Gans, R. O. B. ;
Dullaart, R. P. F. ;
Hospers, G. A. P. .
HUMAN GENE THERAPY, 2006, 17 (06) :683-691
[8]   Basic fibroblast growth factor in patients with intermittent claudication: Results of a phase I trial [J].
Lazarous, DF ;
Unger, EF ;
Epstein, SE ;
Stine, A ;
Arevalo, JL ;
Chew, EY ;
Quyyumi, AA .
JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY, 2000, 36 (04) :1239-1244
[9]   Therapeutic angiogenesis with recombinant fibroblast growth factor-2 for intermittent claudication (the TRAFFIC study): a randomised trial [J].
Lederman, RJ ;
Mendelsohn, FO ;
Anderson, RD ;
Saucedo, JF ;
Tenaglia, AN ;
Hermiller, JB ;
Hillegass, WB ;
Rocha-Singh, K ;
Moon, TE ;
Whitehouse, MJ ;
Annex, BH .
LANCET, 2002, 359 (9323) :2053-2058
[10]   Peripheral arterial disease in patients with diabetes [J].
Marso, SP ;
Hiatt, WR .
JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY, 2006, 47 (05) :921-929