Meuris Bart, Verbeken Erik, Flameng Willem
Department of Cardiac Surgery, Katholieke Universiteit Leuven, Leuven, Belgium.
J Heart Valve Dis. 2005 May;14(3):358-63; discussion 363-4.
Acellularization prevents cell-mediated calcification of the aortic wall, but the inflammatory response towards the unfixed tissue is problematic. Two additional fixation methods, applied after tissue acellularization, were studied.
Porcine aortic wall samples were randomized into four groups: (1) Standard fixation with glutaraldehyde (GA); (2) acellularization by a combined method of enzymes (DNase, RNase) and a detergent (Triton X-100); (3) acellularization followed by standard GA fixation; (4) acellularization followed by photo-oxidation. Samples were implanted into the wall of both jugular veins of six juvenile sheep. Tissue was explanted after three months and evaluated by X-radiography, light and electron microscopy, and calcium content (cc) measurement (atomic absorption spectrometry). Auto-fluorescence of elastic fibers was used to identify the relationship between calcific deposits and elastin.
GA-fixed aortic wall samples showed clear mineralization (cc 41.6 +/- 17.8 microg/mg), occurring predominantly at the level of cell remnants, as confirmed by electron- and fluorescence microscopy, locating calcific deposits in between elastic fibers. Acellularized aortic wall fragments were calcified significantly less, but an important (non-infectious) inflammatory response caused elastolysis and subsequent calcification of the elastic fibers (cc 5.6 +/- 2.8 microg/mg). Acellularized and GA-fixed fragments revealed important, inhomogeneously spread calcific deposits (cc 24.7 +/- 10.0 pg/mg). Photo-oxidized samples remained free from calcification (cc 0.82 +/- 1.6 microg/mg).
Acellularization is a promising tool in the prevention of porcine aortic wall calcification, but additional tissue fixation is necessary to prevent structural degeneration. GA fixation after acellularization causes important inhomogeneous tissue mineralization. Photo-oxidation combines optimal tissue fixation with superior anticalcification characteristics.
脱细胞处理可防止主动脉壁发生细胞介导的钙化,但对未固定组织的炎症反应存在问题。本研究对组织脱细胞处理后应用的另外两种固定方法进行了研究。
将猪主动脉壁样本随机分为四组:(1)用戊二醛(GA)进行标准固定;(2)采用酶(脱氧核糖核酸酶、核糖核酸酶)与去污剂(曲拉通X-100)联合法进行脱细胞处理;(3)脱细胞处理后进行标准GA固定;(4)脱细胞处理后进行光氧化处理。将样本植入6只幼年绵羊的双侧颈静脉壁。3个月后取出组织,通过X射线摄影、光镜和电镜检查以及钙含量(cc)测定(原子吸收光谱法)进行评估。利用弹性纤维的自发荧光来确定钙化沉积物与弹性蛋白之间的关系。
GA固定的主动脉壁样本显示出明显的矿化(cc 41.6±±),主要发生在细胞残余物水平,电镜和荧光显微镜检查证实,钙化沉积物位于弹性纤维之间。脱细胞处理的主动脉壁碎片钙化明显较少,但重要的(非感染性)炎症反应导致弹性纤维溶解并随后钙化(cc 5.6±±)。脱细胞处理并经GA固定的碎片显示出重要的、分布不均匀的钙化沉积物(cc 24.7±±)。光氧化处理的样本未发生钙化(cc 0.82±±)。
脱细胞处理是预防猪主动脉壁钙化的一种有前景的方法,但需要额外的组织固定以防止结构退变。脱细胞处理后进行GA固定会导致重要的不均匀组织矿化。光氧化处理将最佳的组织固定与卓越的抗钙化特性相结合。 17.8微克/毫克 2.8微克/毫克 10.0微克/毫克 1.6微克/毫克