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利用生物光子学工具捕捉胚胎心脏的结构与功能。

Capturing structure and function in an embryonic heart with biophotonic tools.

作者信息

Karunamuni Ganga H, Gu Shi, Ford Matthew R, Peterson Lindsy M, Ma Pei, Wang Yves T, Rollins Andrew M, Jenkins Michael W, Watanabe Michiko

机构信息

Department of Pediatrics, Case Western Reserve University School of Medicine Cleveland, OH, USA.

Department of Biomedical Engineering, Case Western Reserve University School of Engineering Cleveland, OH, USA.

出版信息

Front Physiol. 2014 Sep 23;5:351. doi: 10.3389/fphys.2014.00351. eCollection 2014.

Abstract

Disturbed cardiac function at an early stage of development has been shown to correlate with cellular/molecular, structural as well as functional cardiac anomalies at later stages culminating in the congenital heart defects (CHDs) that present at birth. While our knowledge of cellular and molecular steps in cardiac development is growing rapidly, our understanding of the role of cardiovascular function in the embryo is still in an early phase. One reason for the scanty information in this area is that the tools to study early cardiac function are limited. Recently developed and adapted biophotonic tools may overcome some of the challenges of studying the tiny fragile beating heart. In this chapter, we describe and discuss our experience in developing and implementing biophotonic tools to study the role of function in heart development with emphasis on optical coherence tomography (OCT). OCT can be used for detailed structural and functional studies of the tubular and looping embryo heart under physiological conditions. The same heart can be rapidly and quantitatively phenotyped at early and again at later stages using OCT. When combined with other tools such as optical mapping (OM) and optical pacing (OP), OCT has the potential to reveal in spatial and temporal detail the biophysical changes that can impact mechanotransduction pathways. This information may provide better explanations for the etiology of the CHDs when interwoven with our understanding of morphogenesis and the molecular pathways that have been described to be involved. Future directions for advances in the creation and use of biophotonic tools are discussed.

摘要

发育早期心脏功能紊乱已被证明与后期的细胞/分子、结构及功能心脏异常相关,最终导致出生时出现先天性心脏病(CHD)。虽然我们对心脏发育过程中细胞和分子步骤的了解正在迅速增加,但我们对胚胎中心血管功能作用的理解仍处于早期阶段。该领域信息匮乏的一个原因是研究早期心脏功能的工具有限。最近开发和改进的生物光子学工具可能会克服研究微小脆弱跳动心脏的一些挑战。在本章中,我们描述并讨论我们在开发和应用生物光子学工具以研究功能在心脏发育中的作用方面的经验,重点是光学相干断层扫描(OCT)。OCT可用于在生理条件下对管状和环化胚胎心脏进行详细的结构和功能研究。使用OCT可以在早期和后期快速且定量地对同一颗心脏进行表型分析。当与其他工具如光学标测(OM)和光学起搏(OP)结合使用时,OCT有潜力在空间和时间细节上揭示可能影响机械转导途径的生物物理变化。当这些信息与我们对形态发生以及已描述的相关分子途径的理解相结合时,可能会为CHD的病因提供更好的解释。文中还讨论了生物光子学工具创建和应用方面未来的发展方向。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d9bf/4173643/4be61e8d9be7/fphys-05-00351-g0001.jpg

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