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体内稀有循环细胞的流式细胞术分析。

In Vivo Flow Cytometry of Extremely Rare Circulating Cells.

机构信息

Northeastern University, Department of Electrical and Computer Engineering, Boston, MA, 02115, USA.

Northeastern University, Department of Bioengineering, Boston, MA, 02115, USA.

出版信息

Sci Rep. 2019 Mar 4;9(1):3366. doi: 10.1038/s41598-019-40143-2.

Abstract

Circulating tumor cells (CTCs) are of great interest in cancer research, but methods for their enumeration remain far from optimal. We developed a new small animal research tool called "Diffuse in vivo Flow Cytometry" (DiFC) for detecting extremely rare fluorescently-labeled circulating cells directly in the bloodstream. The technique exploits near-infrared diffuse photons to detect and count cells flowing in large superficial arteries and veins without drawing blood samples. DiFC uses custom-designed, dual fiber optic probes that are placed in contact with the skin surface approximately above a major vascular bundle. In combination with a novel signal processing algorithm, DiFC allows counting of individual cells moving in arterial or venous directions, as well as measurement of their speed and depth. We show that DiFC allows sampling of the entire circulating blood volume of a mouse in under 10 minutes, while maintaining a false alarm rate of 0.014 per minute. In practice, this means that DiFC allows reliable detection of circulating cells below 1 cell per mL. Hence, the unique capabilities of DiFC are highly suited to biological applications involving very rare cell types such as the study of hematogenous cancer metastasis.

摘要

循环肿瘤细胞(CTCs)在癌症研究中备受关注,但目前用于其计数的方法仍远非最佳。我们开发了一种名为“体内弥散流式细胞术”(DiFC)的新型小动物研究工具,用于直接在血流中检测极其罕见的荧光标记循环细胞。该技术利用近红外弥散光子来检测和计数在大浅表动脉和静脉中流动的细胞,而无需抽取血样。DiFC 使用定制的双光纤探头,探头放置在大约位于主要血管束上方的皮肤表面上。结合新颖的信号处理算法,DiFC 允许对沿动脉或静脉方向移动的单个细胞进行计数,并测量其速度和深度。我们表明,DiFC 允许在不到 10 分钟的时间内对小鼠的整个循环血容量进行采样,同时保持每分钟 0.014 的误报率。实际上,这意味着 DiFC 可以可靠地检测到每毫升低于 1 个细胞的循环细胞。因此,DiFC 的独特功能非常适合涉及非常罕见细胞类型的生物学应用,例如研究血液癌转移。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f59f/6399281/f9a757cb5848/41598_2019_40143_Fig1_HTML.jpg

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