Control of cardiac waves in human iPSC-CM syncytia by a Halbach array and magnetic nanoparticles.

The Halbach array, originally developed for particle accelerators, is a compact arrangement of permanent magnets that creates well-defined magnetic fields without heating. Here, we demonstrate its use for modulating the speed of electromechanical waves in cardiac syncytia of human stem cell-derived cardiomyocytes. At 40-50 mT magnetic field strength, a cylindrical dipolar Halbach array boosted the conduction velocity, CV, by up to 25% when the magnetic field was co-aligned with the electromechanical wave (but not when perpendicular to it).

Paradoxical effects of ZIM3, a CRISPRi effector, on human induced pluripotent stem-cell-derived cardiomyocyte electrophysiology.

We show that zinc finger imprinted 3 (Zim3), when used as Zim3-KRAB-dCas9 effector in interference CRISPR, without any guide RNAs, paradoxically up-regulates key cardiac ion channel genes in human-induced pluripotent stem-cell-derived cardiomyocytes (iPSC-CMs), responsible for healthy resting membrane potential, repolarization of the action potential, and electrical transmission of signals. These were found to yield expected functional enhancements consistent with a more mature iPSC-CM phenotype, with potentially desirable properties.

OptoDyCE-plate as an affordable high throughput imager for all optical cardiac electrophysiology.

We present a simple low-cost system for comprehensive functional characterization of cardiac function under spontaneous and paced conditions, in standard 96 and 384-well plates. This full-plate actuator/imager, OptoDyCE-plate, uses optogenetic stimulation and optical readouts of voltage and calcium (parallel recordings from up to 100 wells in 384-well plates are demonstrated). The system is validated with syncytia of human induced pluripotent stem cell derived cardiomyocytes, iPSC-CMs, grown as monolayers, or in quasi-3D isotropic and anisotropic constructs using electrospun matrices, in 96 and 384-well format.

CRISPRi gene modulation and all-optical electrophysiology in post-differentiated human iPSC-cardiomyocytes.

Uncovering gene-phenotype relationships can be enabled by precise gene modulation in human induced pluripotent stem-cell-derived cardiomyocytes (iPSC-CMs) and follow up phenotyping using scalable all-optical electrophysiology platforms. Such efforts towards human functional genomics can be aided by recent CRISPR-derived technologies for reversible gene inhibition or activation (CRISPRi/a). We set out to characterize the performance of CRISPRi in post-differentiated iPSC-CMs, targeting key cardiac ion channel genes, KCNH2, KCNJ2, and GJA1, and providing a multiparametric quantification of the effects on cardiac repolarization, stability of the resting membrane potential and conduction properties using all-optical tools.

OptoDyCE-plate as an affordable high throughput imager for all optical cardiac electrophysiology.

We present a simple low-cost system for comprehensive functional characterization of cardiac function under spontaneous and paced conditions, in standard 96 and 384-well plates. This full-plate actuator/imager, OptoDyCE-plate, uses optogenetic stimulation and optical readouts of voltage and calcium from all wells in parallel. The system is validated with syncytia of human induced pluripotent stem cell derived cardiomyocytes, iPSC-CMs, grown as monolayers, or in quasi-3D isotropic and anisotropic constructs using electrospun matrices, in 96 and 394-well format.

CRISPRi Gene Modulation and All-Optical Electrophysiology in Post-Differentiated Human iPSC-Cardiomyocytes.

Uncovering gene-phenotype relationships can be enabled by precise gene modulation in human induced pluripotent stem-cell-derived cardiomyocytes (iPSC-CMs) and follow up phenotyping using scalable all-optical electrophysiology platforms. Such efforts towards human functional genomics can be aided by recent CRISPR-derived technologies for reversible gene inhibition or activation (CRISPRi/a). We set out to characterize the performance of CRISPRi in post-differentiated iPSC-CMs, targeting key cardiac ion channel genes, KCNH2, KCNJ2, and GJA1, and providing a multiparametric quantification of the effects on cardiac repolarization, stability of the resting membrane potential and conduction properties using all-optical tools.

Portable low-cost macroscopic mapping system for all-optical cardiac electrophysiology.

Significance: All-optical cardiac electrophysiology enables the visualization and control of key parameters relevant to the detection of cardiac arrhythmias. Mapping such responses in human induced pluripotent stem-cell-derived cardiomyocytes (hiPSC-CMs) is of great interest for cardiotoxicity and personalized medicine applications.

Aim: We introduce and validate a very low-cost compact mapping system for macroscopic all-optical electrophysiology in layers of hiPSC-CMs.

Portable device to determine particle asymmetry parameter.

Accurate characterization of the asymmetry parameter g is of crucial importance for radiative transfer calculations. Here, we present a portable light scattering (PLS) device designed for in situ, real-time, and contact-free measurements of the particle phase function. The integration time is 20ms for each measurement.

Generation of aerosol-particle light-scattering patterns from digital holograms.

The similarity between the light-scattering pattern of a particle in the near-forward direction and diffraction from the particle's silhouette is investigated. Images of irregularly shaped free-flowing aerosol particles are obtained from digital hologram measurements, which are then binarized to yield a silhouette. Application of Huygens's principle to the silhouette generates an approximate scattering pattern, which when compared to the true measured pattern shows good agreement for particles much larger than the wavelength of light.

Solving the inverse problem for coarse-mode aerosol particle morphology with digital holography.

Coarse mode atmospheric aerosol particles are abundant in agricultural, desert, and urban environments. Accurate characterisation of these particles' morphology is an important need in scientific and applied contexts, especially to advance our understanding for how such aerosols influence solar radiative forcing of the atmosphere. Elastic light scattering is a standard method to study aerosol particles in a contact-free manner, wherein measured scattering patterns are interpreted to infer particle morphology.

Quasi-three-dimensional particle imaging with digital holography.

In this work, approximate three-dimensional structures of microparticles are generated with digital holography using an automated focus method. This is done by stacking a collection of silhouette-like images of a particle reconstructed from a single in-line hologram. The method enables estimation of the particle size in the longitudinal and transverse dimensions.

Backscattering measurements of micron-sized spherical particles.

An apparatus was designed and assembled to measure scattered light in the range of 180°±6° where enhanced backscattering, the cause of a glory, occurs. The apparatus was calibrated and tested using Fraunhofer circular aperture diffraction, angle of incidence correction, and a diffuse reflector. Theory indicates that backscattering is strongly dependent on particle size, refractive index, and shape.