Previous Page  94 / 155 Next Page
Information
Show Menu
Previous Page 94 / 155 Next Page
Page Background

Single-Cell Biophysics: Measurement, Modulation, and Modeling

Poster Abstracts

89 

89-POS

Board 45

Detection and Characterization of Spontaneous Calcium Release Events in Cardiac

Myocytes

Alex Vallmitjana

1

, Carmen Tarifa

2

, Raul Benitez

1

.Leif Hove-Madsen

2

.

2

Institut Català de Ciències Cardiovasculars, Barcelona, Spain.

1

Universitat Politècnica de

Catalunya, Barcelona, Spain,

In cardiac function, calcium handling plays a critical role since it is responsible of the excitation-

contraction coupling at the cellular level. Indeed, the spontaneous release of intracellular calcium

in cardiac cells is a well-established mechanism underlying cardiac arrhythmias among other

heart pathologies. An accurate, robust detection of such spatio-temporal patterns is key to further

understand the cell physiology mechanisms underlying cardiac function and disease.

Most cell level studies in the past have focused in linescan (X-T) images which do not capture

spatial characteristics such as the release area, spatial dynamics or the localization with respect to

nearby subcellular structures.

We have developed an automatic image processing system that allows detecting, localizing and

characterizing calcium release events from a sequence of live cell fluorescence microscopy

images. The system is able to process both linescan and framescan (X-Y-T) image sequences and

detect different event release types such as sparks and calcium waves.

The system uses a multilevel wavelet analysis in order to identify events with a duration within a

given temporal range and a modified watershed segmentation algorithm in to determine the

space-time shape and centroid of the event. The event candidates are further filtered out using

morphological features such as amplitude, full width at half maximum or characteristic decay

time.

The method has been applied to an experimental database previously validated by a human

expert including a total of 621 events from 8 human atrial cardiomyocytes. As a measure of

overall performance, the approach achieves an average area under the ROC curve (AUC) of 0.8

with a standard error of 0.017.