Parsons-Wingerter Patricia, Reinecker Hans-Christian
Research & Technology Directorate, John H. Glenn Research Center, National Aeronautics and Space Administration, Cleveland, OH 44135.
Department of Medicine, Division of Gastroenterology and Center for the Study of Inflammatory Bowel Disease, Massachusetts General Hospital and Harvard Medical School, GRJ R708, Fruit Street, Boston, MA 02114.
Gravit Space Biol Bull. 2012 Oct 1;26(2):2-12.
Challenges to long-duration space exploration and colonization in microgravity and cosmic radiation environments by humans include poorly understood risks for gastrointestinal function and cancer. Nonetheless, constant remodeling of the intestinal microvasculature is critical for tissue viability, healthy wound healing, and successful prevention or recovery from vascular-mediated inflammatory or ischemic diseases such as cancer. Currently no automated image analysis programs provide quantitative assessments of the complex structure of the mucosal vascular system that are necessary for tracking disease development and tissue recovery. Increasing abnormalities to the microvascular network geometry were therefore mapped with VESsel GENeration Analysis (VESGEN) software from 3D tissue reconstructions of developing intestinal inflammation in a dextran sulfate sodium (DSS) mouse model. By several VESGEN parameters and a novel vascular network linking analysis, inflammation strongly disrupted the regular, lattice-like geometry that defines the normal microvascular network, correlating positively with the increased recruitment of dendritic cells during mucosal defense responses.
人类在微重力和宇宙辐射环境中进行长期太空探索和殖民面临的挑战包括对胃肠功能和癌症风险的了解不足。尽管如此,肠道微血管的持续重塑对于组织活力、健康的伤口愈合以及成功预防或从血管介导的炎症或缺血性疾病(如癌症)中恢复至关重要。目前,没有自动化图像分析程序能够对黏膜血管系统的复杂结构进行定量评估,而这种评估对于跟踪疾病发展和组织恢复是必不可少的。因此,利用VESsel GENeration Analysis(VESGEN)软件,从硫酸葡聚糖钠(DSS)小鼠模型中发育性肠道炎症的三维组织重建图中,绘制出微血管网络几何结构日益增加的异常情况。通过几个VESGEN参数和一种新型的血管网络连接分析,炎症严重破坏了定义正常微血管网络的规则、格子状几何结构,这与黏膜防御反应期间树突状细胞募集增加呈正相关。