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Determination of the polarization states of an arbitrary polarized terahertz beam: vectorial vortex analysis.

ABSTRACT: Vectorial vortex analysis is used to determine the polarization states of an arbitrarily polarized terahertz (0.1-1.6 THz) beam using THz achromatic axially symmetric wave (TAS) plates, which have a phase retardance of Δ = 163° and are made of polytetrafluorethylene. Polarized THz beams are converted into THz vectorial vortex beams with no spatial or wavelength dispersion, and the unknown polarization states of the incident THz beams are reconstructed. The polarization determination is also demonstrated at frequencies of 0.16 and 0.36 THz. The results obtained by solving the inverse source problem agree with the values used in the experiments. This vectorial vortex analysis enables a determination of the polarization states of the incident THz beam from the THz image. The polarization states of the beams are estimated after they pass through the TAS plates. The results validate this new approach to polarization detection for intense THz sources. It could find application in such cutting edge areas of physics as nonlinear THz photonics and plasmon excitation, because TAS plates not only instantaneously elucidate the polarization of an enclosed THz beam but can also passively control THz vectorial vortex beams.

SUBMITTER: Wakayama T

PROVIDER: S-EPMC4371186 | biostudies-other | 2015

REPOSITORIES: biostudies-other

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Project description:Hepatitis E virus (HEV) is a common cause of acute viral hepatitis worldwide. Most HEV infections are asymptomatic, but immunocompromised patients infected with HEV genotype 3 (HEV3), HEV4, or HEV7 may develop chronic infections. The HEV particles in stools are naked (nHEV), while those in the serum and culture supernatants (eHEV) are associated with lipids. Hepatocytes are polarized epithelial cells that have basolateral (oriented toward the blood) and apical (oriented toward the bile) exosomal pathways. We isolated a subclone, F2, from the human hepatocarcinoma cell line HepG2/C3A that grew as a polarized monolayer culture and had better HEV production than HepG2/C3A cells. F2 cells cultured on semipermeable collagen inserts and infected basolaterally with nHEV3 released 94.6% of virus particles apically, those infected with eHEV3 released 96.8% apically, and eHEV1-infected cells released 99.3% apically. Transcytosis was not involved. Density gradient centrifugation and NP-40 treatment showed that HEV particles released both apically and basolaterally were lipid associated. The apically released HEV3 and HEV1 particles were six and nine times more infectious than those released basolaterally, respectively. Confocal microscopy indicated that the open reading frame 2 (ORF2) capsid protein colocalized apically with ORF3 virus protein, the apical marker DPP4, and the recycling endosome GTPase Rab27a. The amounts of soluble glycosylated ORF2 secreted apically and basolaterally were similar. These polarized-hepatocyte data suggest that infectious HEV particles are mainly released into bile, while the small fraction released into blood could spread HEV throughout the host.IMPORTANCE Hepatitis E virus (HEV) in stools is naked, while that in culture supernatants and patients' blood is lipid associated. Its life cycle in hepatocytes, polarized cells with a basolateral side communicating with blood and an apical side connected with bile, is incompletely understood. We have developed a polarized hepatocyte model and used the cells to analyze the supernatants bathing the apical and basolateral sides and HEV subcellular distribution. HEV particles from both sides were lipid associated, and most infectious HEV particles left the cell via its apical side. Similar amounts of the open reading frame 2 (ORF2) soluble capsid protein were secreted from both sides of the hepatocytes. This model mimicking physiological conditions should help clarify the HEV cell cycle in polarized hepatocytes.

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Determination of the polarization states of an arbitrary polarized terahertz beam: vectorial vortex analysis.

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