Bioengineered analog of stromal cell-derived factor 1α preserves the biaxial mechanical properties of native myocardium after infarction

被引:12
|
作者
Wang, Hanjay [1 ]
Wisneski, Andrew [2 ]
Paulsen, Michael J. [1 ]
Imbrie-Moore, Annabel [1 ,3 ]
Wang, Zhongjie [2 ]
Xuan, Yue [2 ]
Hernandez, Hector Lopez [4 ]
Lucian, Haley J. [1 ]
Eskandari, Anahita [1 ]
Thakore, Akshara D. [1 ]
Parry, Justin M. [1 ]
Hironaka, Camille E. [1 ]
von Bornstaedt, Daniel [1 ]
Steele, Amanda N. [1 ,5 ]
Stapleton, Lyndsay M. [1 ,5 ]
Williams, Kiah M. [1 ]
Wu, Matthew A. [1 ]
MacArthur, John W., Jr. [1 ]
Woo, Y. Joseph [1 ,5 ]
机构
[1] Stanford Univ, Dept Cardiothorac Surg, Falk Bldg CV 235,300 Pasteur Dr, Stanford, CA 94305 USA
[2] Univ Calif San Francisco, Dept Surg, San Francisco, CA USA
[3] Stanford Univ, Dept Mech Engn, Stanford, CA 94305 USA
[4] Stanford Univ, Dept Mat Sci & Engn, Stanford, CA 94305 USA
[5] Stanford Univ, Dept Bioengn, Stanford, CA 94305 USA
基金
美国国家卫生研究院;
关键词
Biaxial tension; Myocardial infarction; Ventricular remodeling; Angiogenic therapy; NEOVASCULOGENIC THERAPY; VENTRICULAR-FUNCTION; FACTOR-1-ALPHA; BIOMECHANICS; STIFFNESS; STRAIN; TISSUE; RAT;
D O I
10.1016/j.jmbbm.2019.04.014
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
Adverse remodeling of the left ventricle (LV) after myocardial infarction (MI) results in abnormal tissue biomechanics and impaired cardiac function, often leading to heart failure. We hypothesized that intramyocardial delivery of engineered stromal cell-derived factor la analog (ESA), our previously-developed supra-efficient proangiogenic chemokine, preserves biaxial LV mechanical properties after MI Male Wistar rats (n = 45) underwent sham surgery (n = 15) or permanent left anterior descending coronary artery ligation. Rats sustaining MI were randomized for intramyocardial injections of either saline (100 mu L, n = 15) or ESA (6 mu g/kg, n = 15), delivered at four standardized borderzone sites. After 4 weeks, echocardiography was performed, and the hearts were explanted. Tensile testing of the anterolateral LV wall was performed using a displacement-controlled biaxial load frame, and modulus was determined after constitutive modeling. At 4 weeks post-MI, compared to saline controls, ESA-treated hearts had greater wall thickness (1.68 +/- 0.05 mm vs 1.42 +/- 0.08 mm, p = 0.008), smaller end-diastolic LV internal dimension (6.88 +/- 0.29 mm vs 7.69 +/- 0.22 mm, p = 0.044), and improved ejection fraction (62.8 +/- 3.0% vs 49.4 +/- 4.5%, p = 0.014). Histologic analysis revealed significantly reduced infarct size for ESA-treated hearts compared to saline controls (29.4 +/- 2.9% vs 41.6 +/- 3.1%, p = 0.021). Infarcted hearts treated with ESA exhibited decreased modulus compared to those treated with saline in both the circumferential (211.5 +/- 6.9 kPa vs 264.3 +/- 12.5 kPa, p = 0.001) and longitudinal axes (194.5 +/- 6.5 kPa vs 258.1 +/- 14.4 kPa, p < 0.001). In both principal directions, ESA-treated infarcted hearts possessed similar tissue compliance as sham non-infarcted hearts. Overall, intramyocardial ESA therapy improves post-MI ventricular remodeling and function, reduces infarct size, and preserves native LV biaxial mechanical properties.
引用
收藏
页码:165 / 171
页数:7
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