scholarly journals A Motion Correction Framework for Time Series Sequences in Microscopy Images

2013 ◽  
Vol 19 (2) ◽  
pp. 433-450 ◽  
Author(s):  
Ankur N. Kumar ◽  
Kurt W. Short ◽  
David W. Piston

AbstractWith the advent of in vivo laser scanning fluorescence microscopy techniques, time-series and three-dimensional volumes of living tissue and vessels at micron scales can be acquired to firmly analyze vessel architecture and blood flow. Analysis of a large number of image stacks to extract architecture and track blood flow manually is cumbersome and prone to observer bias. Thus, an automated framework to accomplish these analytical tasks is imperative. The first initiative toward such a framework is to compensate for motion artifacts manifest in these microscopy images. Motion artifacts in in vivo microscopy images are caused by respiratory motion, heart beats, and other motions from the specimen. Consequently, the amount of motion present in these images can be large and hinders further analysis of these images. In this article, an algorithmic framework for the correction of time-series images is presented. The automated algorithm is comprised of a rigid and a nonrigid registration step based on shape contexts. The framework performs considerably well on time-series image sequences of the islets of Langerhans and provides for the pivotal step of motion correction in the further automatic analysis of microscopy images.

2020 ◽  
Vol 11 (1) ◽  
Author(s):  
Jiang Lan Fan ◽  
Jose A. Rivera ◽  
Wei Sun ◽  
John Peterson ◽  
Henry Haeberle ◽  
...  

AbstractUnderstanding the structure and function of vasculature in the brain requires us to monitor distributed hemodynamics at high spatial and temporal resolution in three-dimensional (3D) volumes in vivo. Currently, a volumetric vasculature imaging method with sub-capillary spatial resolution and blood flow-resolving speed is lacking. Here, using two-photon laser scanning microscopy (TPLSM) with an axially extended Bessel focus, we capture volumetric hemodynamics in the awake mouse brain at a spatiotemporal resolution sufficient for measuring capillary size and blood flow. With Bessel TPLSM, the fluorescence signal of a vessel becomes proportional to its size, which enables convenient intensity-based analysis of vessel dilation and constriction dynamics in large volumes. We observe entrainment of vasodilation and vasoconstriction with pupil diameter and measure 3D blood flow at 99 volumes/second. Demonstrating high-throughput monitoring of hemodynamics in the awake brain, we expect Bessel TPLSM to make broad impacts on neurovasculature research.


1995 ◽  
Vol 10 (2) ◽  
pp. 168-181 ◽  
Author(s):  
N.H. Staalsen ◽  
M. Ulrich ◽  
W.Y. Kim ◽  
E.M. Pedersen ◽  
T.V. How ◽  
...  

Author(s):  
Satoyuki Kawano ◽  
Takuma Kato ◽  
Kazuhiro Nakahashi ◽  
Atsushi Shirai ◽  
Toshiyuki Hayase ◽  
...  

To effectively design the vibrating flow pump (VFP) for left ventricular assist device, the numerical codes were developed for three-dimensional blood flow based on the finite volume method. The numerical codes were also developed based on the artificial compressibility method by the use of unstructured grid. Three-dimensional numerical computations and the visualizations were made for flow patterns in the casing of VFP, which were closely connected with hemolysis and blood coagulation. We examined the three different inlet conditions, i.e., radial flow, flow considering the 2nd vibration mode of the jellyfish valve motion, and the swirling flow, to explore the suitable condition for preventing the hemolysis and the blood coagulation. It was found that the swirling flow could effectively decrease hemolysis. The effect of rheology model of the blood flow was also studied in detail.


2014 ◽  
Vol 5 (12) ◽  
pp. 4131 ◽  
Author(s):  
Nathan D. Shemonski ◽  
Shawn S. Ahn ◽  
Yuan-Zhi Liu ◽  
Fredrick A. South ◽  
P. Scott Carney ◽  
...  

2020 ◽  
Vol 20 (10) ◽  
pp. 2040027
Author(s):  
YUSHU LIU ◽  
LIPING MA ◽  
WEI GAO ◽  
ZHICHENG LIU ◽  
SHOUXIN WANG ◽  
...  

Understanding the relationship between the changes in the axonal transport of the optic nerve (ON) and lamina cribrosa (LC) deformation will be helpful to estimate the degree of axonal transport block by measuring the LC deformation in vivo. First, the changes in the axonal transport of the ON were studied using an acute high intraocular pressure (IOP) model, which was established by perfusing saline water into the anterior chamber of cats. The IOP of cat was unilaterally elevated to and maintained at 30, 40, and 50[Formula: see text]mmHg. The axonal transport of the ON was examined by confocal laser scanning microscope. Then the deformations and stress distributions of the LC and ON were calculated using a three-dimensional finite element model of the LC microstructure including ON. The results showed axonal transport changes of ON increased with elevation of the IOPs. While Young’s modulus of the LC and ON were assumed as 0.1[Formula: see text]MPa and 0.03[Formula: see text]MPa, the numerical simulation results showed that LC had displacements of 0.02, 0.03, and 0.04[Formula: see text]mm backward at the IOPs of 30, 40, and 50[Formula: see text]mmHg, respectively. The calculated compressive strain applied to the ON were 0.0425, 0.0567, and 0.0709 under 30, 40, and 50[Formula: see text]mmHg IOP, respectively. The results of strain and stress analysis of LC and ON showed that the deformation of LC would compress the ON. The axonal transport abnormalities could be inferred by measuring the LC deformation in vivo.


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