Lucidarme Olivier, Nguyen Thai, Kono Yuko, Corbeil Jacqueline, Choi Sang-Hee, Varner Judith, Mattrey Robert F
Department of Radiology, University of California, San Diego, CA, USA.
Acad Radiol. 2004 Jan;11(1):4-12. doi: 10.1016/s1076-6332(03)00575-0.
To optimize an angiogenesis model for imaging research that is stable and can be imaged several times over the angiogenic time course.
Mice and rats received two injections of 0.4 mL of extract of basement membrane matrix (Matrigel; Becton Dickinson Labware, Bedford, MA) in the subcutaneous spaces on either side of the spine. One of the two Matrigel plugs in each animal had either 0.1 microg/mL of basic fibroblast growth factor (bFGF) (11 mice), 1.0 microg/mL of bFGF (12 mice, 5 rats), or 1.0 microg/mL of bFGF and 60 U/mL of heparin (11 mice). Three to 12 days after implantation, animals were imaged before and after the administration of up to four injections of 0.1 mL AF0150. Phase inversion imaging was used on a Siemens Elegra (Siemens ultrasound, Issaquah, WA) equipped with a 13 MHz VFX transducer. Three observers subjectively assessed the pattern of enhancement using a four-point scale. The Matrigel plugs were then removed and two observers graded the angiogenic response on a four-point scale. Ten Matrigel plugs, five with 1.0 microg/mL bFGF and five without, were evaluated histologically following immunohistochemical staining with anti-CD31.
The angiogenic response was greater in Matrigel plugs with 1.0 than with 0.1 microg/mL of bFGF. Heparin did not increase the angiogenic response. Vessels were predominantly at the periphery of the plugs with variable central penetration. Plugs appeared anechoic and homogeneous on ultrasound. Contrast enhancement within the plug occurred in 44% of mice with an angiogenic response at or after day 6 and the enhancement increased with the angiogenic response. In the others, peripheral enhancement could not be distinguished from the enhancement of surrounding tissues that were also hyperemic. The thicker rat skin interfered with plug assessment.
A stable angiogenesis model without the complexity of tumors is described. This model offers the opportunity to image the development and/or inhibition of angiogenesis. Neovasculature in Matrigel was detectable using ultrasound contrast. Quantitative studies correlating the degree of enhancement to microvascular density will be determined in subsequent studies.
优化一种用于成像研究的血管生成模型,该模型稳定且能在血管生成的时间进程中多次成像。
小鼠和大鼠在脊柱两侧的皮下空间接受两次0.4 mL基底膜基质提取物(基质胶;贝迪实验室用品公司,马萨诸塞州贝德福德)注射。每只动物的两个基质胶塞中,一个含有0.1 μg/mL碱性成纤维细胞生长因子(bFGF)(11只小鼠)、1.0 μg/mL bFGF(12只小鼠、5只大鼠),或1.0 μg/mL bFGF和60 U/mL肝素(11只小鼠)。植入后3至12天,在给予多达四次0.1 mL AF0150注射前后对动物进行成像。使用配备13 MHz VFX换能器的西门子Elegra(西门子超声,华盛顿州伊斯萨夸)进行相反转成像。三名观察者使用四点量表主观评估增强模式。然后取出基质胶塞,两名观察者使用四点量表对血管生成反应进行分级。在用抗CD31进行免疫组织化学染色后,对十个基质胶塞(五个含1.0 μg/mL bFGF,五个不含)进行组织学评估。
含1.0 μg/mL bFGF的基质胶塞中的血管生成反应比含0.1 μg/mL bFGF的更强。肝素未增加血管生成反应。血管主要位于胶塞周边,中央穿透情况各异。胶塞在超声上表现为无回声且均匀。在第6天及之后出现血管生成反应的44%的小鼠中,胶塞内有造影剂增强,且增强程度随血管生成反应增加。在其他小鼠中,周边增强与周围充血组织的增强无法区分。较厚的大鼠皮肤干扰了胶塞评估。
描述了一种无肿瘤复杂性的稳定血管生成模型。该模型为成像血管生成的发展和/或抑制提供了机会。使用超声造影可检测基质胶中的新生血管。后续研究将确定将增强程度与微血管密度相关联的定量研究。