Electrical & Computer Engineering; University of California; Santa Barbara, CA USA.
Organogenesis. 2009 Oct;5(4):248-55. doi: 10.4161/org.5.4.10568.
In the developing heart, time-lapse imaging is particularly challenging. Changes in heart morphology due to tissue growth or long-term reorganization are difficult to follow because they are much subtler than the rapid shape changes induced by the heartbeat. Therefore, imaging heart development usually requires slowing or stopping the heart. This, however, leads to information loss about the unperturbed heart shape and the dynamics of heart function. To overcome this limitation, we have developed a non-invasive heart imaging technique to jointly document heart function (at fixed stages of development) as well as its morphogenesis (at any fixed phase in the heartbeat) that does not require stopping or slowing the heart. We review the challenges for imaging heart development and our methodology, which is based on computationally combining and analyzing multiple high-speed image sequences acquired throughout the course of development. We present results obtained in the developing zebrafish heart. Image analysis of the acquired data yielded blood flow velocity maps and made it possible to follow the relative movement of individual cells over several hours.
在心脏发育过程中,延时成像特别具有挑战性。由于组织生长或长期重组导致的心脏形态变化很难被跟踪,因为它们比心跳引起的快速形状变化要微妙得多。因此,成像心脏发育通常需要减缓或停止心脏跳动。然而,这会导致有关未受干扰的心脏形状和心脏功能动力学的信息丢失。为了克服这一限制,我们开发了一种非侵入性心脏成像技术,可联合记录心脏功能(在发育的固定阶段)及其形态发生(在心跳的任何固定阶段),而无需停止或减缓心脏跳动。我们回顾了成像心脏发育的挑战以及我们的方法,该方法基于对在发育过程中获取的多个高速图像序列进行组合和分析。我们展示了在发育中的斑马鱼心脏中获得的结果。对获取的数据进行图像分析可以生成血流速度图,并能够在数小时内跟踪单个细胞的相对运动。