Optimization of Vascular Casting for Three-Dimensional Fluorescence Cryo-Imaging of Collateral Vessels in the Ischemic Rat Hindlimb. (23rd February 2017)

• Record Type: Journal Article
• Authors: Schwarz, Janina C.V.; van Lier, Monique G.J.T.B.; Bakker, Erik N.T.P.; de Vos, Judith; Spaan, Jos A.E.; VanBavel, Ed; Siebes, Maria
• Is Part Of: Microscopy and microanalysis. Volume 23:Number 1(2017)
• Page Start: 77
• Page End: 87
• Publication Date: 2017-02-23
• Subjects: 3D imaging, -- vascular imaging, -- vascular casting, -- hindlimb ischemia, -- collateral vessels; Microscopy -- Periodicals; Microchemistry -- Periodicals; 502.82
• DOI: 10.1017/S1431927617000095
• Languages: English
• ISSNs: 1431-9276

Abstract

Abstract: Development of collateral vessels, arteriogenesis, may protect against tissue ischemia, however, quantitative data on this process remain scarce. We have developed a technique for replicating the entire arterial network of ischemic rat hindlimbs in three dimensions (3D) based on vascular casting and automated sequential cryo-imaging. Various dilutions of Batson's No. 17 with methyl methacrylate were evaluated in healthy rats, with further protocol optimization in ischemic rats. Penetration of the resin into the vascular network greatly depended on dilution; the total length of casted vessels below 75 µ m was 13-fold higher at 50% dilution compared with the 10% dilution. Dilutions of 25–30%, with transient clamping of the healthy iliac artery, were optimal for imaging the arterial network in unilateral ischemia. This protocol completely filled the lumina of small arterioles and collateral vessels. These appeared as thin anastomoses in healthy legs and increasingly larger vessels during ligation (median diameter 1 week: 63 µ m, 4 weeks: 127 µ m). The presented combination of quality casts with high-resolution cryo-imaging enables automated, detailed 3D analysis of collateral adaptation, which furthermore can be combined with co-registered 3D distributions of fluorescent molecular imaging markers reflecting biological activity or perfusion.