通过虚拟病理学揭示子宫血管网络。

Tsafrir S Kolatt, Yoel Shufaro, Shlomo Mashiach, Bernard Czernobilsky, Sarit Aviel-Ronen, Liat Apel-Sarid, Mazal Dahan, Yuval Or
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引用次数: 0

摘要

背景:任何身体组织在任何时刻的血管网络分布情况,都可能提供有关组织状况及其血管生成功能的宝贵信息。子宫内膜的血管三维网络会在平均 4 周的较短时间内发生变化。人们普遍认为,血管生成与胚胎植入的成败密切相关:我们的研究旨在提出一种在整个子宫周期中跟踪子宫内膜表层血管分布三维演变的方法:方法:该方法利用观察到的血管宽带颜色差异来评估血管在子宫内膜组织表面下的深度坐标。我们利用不同周期天数的新鲜、体外子宫内膜样本的显微图像实施了该方法,以获得人类和动物(猪)样本表层血管群的统计演变轨迹:结果:在人类样本中,我们观察到不同组织深度的浅表血管直径分布呈系统一致的趋势。结果:在人类样本中,我们观察到不同组织深度的 BV 直径分布有一个系统且一致的趋势,我们证明了这一趋势的大小在整个雌性周期中都在演变:更广泛的意义:这种方法有可能进一步加深我们对子宫内膜以外组织血管生成机制的理解。我们认为这种方法还有助于更精确地确定子宫内膜的时间,并有助于更准确地确定试管婴儿治疗中的胚胎移植时间。
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Revealing the uterine blood vessel network via virtual pathology.

Background: The distribution of the blood vessel network at any point in time in any body tissue, may provide valuable information with regards to the tissue condition and its angiogenesis functionality. The blood vessel three-dimensional network of the endometrium goes through a process of change over a relatively short period of 4 weeks on average. It is well accepted that this angiogenesis is closely related to the success or failure of the implantation of the embryo Objective and rationale: Our study aims to present a method to follow the three-dimensional evolution of the superficial blood vessel distribution in the endometrium throughout the uterine cycle.

Method: This method utilizes differences in the observed broadband colors of the blood vessels in order to assess their depth coordinate below the endometrial tissue surface. We implemented the method using microscopic images of fresh, ex-vivo, endometrial samples of different cycle days to obtain the statistical evolution track of the superficial blood vessel population in both human and animal (swine) samples.

Outcomes: In human samples we observed a systematic and consistent trend in the BV diameter distribution at different tissue depths. We demonstrate that the magnitude of this trend evolves throughout the course of the female cycle.

Wider implications: This method has the potential to further our understanding of the mechanisms of angiogenesis in tissues other than the endometrium. We propose that this method may also contribute to more precise endometrial dating and may assist in more accurate determination of embryo transfer timing within IVF treatments.

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