High-speed two-photon polymerization 3D printing with a microchip laser at its fundamental wavelength

High-resolution, high-speed 3D printing by two-photon polymerization (2PP) with a Nd:YVO4 Q-switched microchip laser at its fundamental wavelength of 1064 nm is demonstrated. Polymerization scan speeds of up to 20 mm/s and feature sizes of 250 nm are achieved using a high repetition rate Q-switched microchip laser with a semiconductor saturable absorber mirror (SESAM) and photoresist with a new photo-initiator bearing 6-dialkylaminobenzufuran as electron donor and indene-1,3-dione moiety as electron acceptor. The obtained results demonstrate the high potential of Q-switched microchip lasers for applications in 2PP 3D printing

Nanofabrication of High-Resolution Periodic Structures with a Gap Size Below 100 nm by Two-Photon Polymerization

In this paper, approaches for the realization of high-resolution periodic structures with gap sizes at sub-100 nm scale by two-photon polymerization (2PP) are presented. The impact of laser intensity on the feature sizes and surface quality is investigated. The influence of different photosensitive materials on the structure formation is compared. Based on the elliptical geometry character of the voxel, the authors present an idea to realize high-resolution structures with feature sizes less than 100 nm by controlling the laser focus position with respect to the glass substrate. This investigation covers structures fabricated respectively in the plane along and perpendicular to the major axis of voxel. The authors also provide a useful approach to manage the fabrication of proposed periodic structure with a periodic distance of 200 nm and a gap size of 65 nm

Author Correction: Heparanase-2 protects from LPS-mediated endothelial injury by inhibiting TLR4 signalling

The Acknowledgements section in the original version of this Article was incomplete. “We are grateful to Prof. Israel Vlodavsky (Technion, Haifa, Israel) for giving us 1c7 antibody to HPSE2. We are grateful to Prof. Fridrich Luft for critical editing the manuscript. Grants from German Federal Ministry of Education and Research (BMBF) Nr. 031A577A and 031A577B funded this research. This work was also supported by a grant for the German Research Council to H.H. Ha1388/17-1.” now reads: “We are grateful to Prof. Israel Vlodavsky (Technion, Haifa, Israel) for giving us 1c7 antibody to HPSE2. We are grateful to Prof. Fridrich Luft for critical editing the manuscript. Grants from German Federal Ministry of Education and Research (BMBF) Nr. 031A577A and 031A577B funded this research. This work was also supported by a grant for the German Research Council to H.H. Ha1388/17-1. This work was also supported by a grant from the Else Kröner-Fresenius-Stiftung (EKFS): Grant 2017_A96.” The original Article has been corrected

Heparanase-2 protects from LPS-mediated endothelial injury by inhibiting TLR4 signalling

The endothelial glycocalyx and its regulated shedding are important to vascular health. Endo-β-D-glucuronidase heparanase-1 (HPSE1) is the only enzyme that can shed heparan sulfate. However, the mechanisms are not well understood. We show that HPSE1 activity aggravated Toll-like receptor 4 (TLR4)-mediated response of endothelial cells to LPS. On the contrary, overexpression of its endogenous inhibitor, heparanase-2 (HPSE2) was protective. The microfluidic chip flow model confirmed that HPSE2 prevented heparan sulfate shedding by HPSE1. Furthermore, heparan sulfate did not interfere with cluster of differentiation-14 (CD14)-dependent LPS binding, but instead reduced the presentation of the LPS to TLR4. HPSE2 reduced LPS-mediated TLR4 activation, subsequent cell signalling, and cytokine expression. HPSE2-overexpressing endothelial cells remained protected against LPS-mediated loss of cell-cell contacts. In vivo, expression of HPSE2 in plasma and kidney medullary capillaries was decreased in mouse sepsis model. We next applied purified HPSE2 in mice and observed decreases in TNFα and IL-6 plasma concentrations after intravenous LPS injections. Our data demonstrate the important role of heparan sulfate and the glycocalyx in endothelial cell activation and suggest a protective role of HPSE2 in microvascular inflammation. HPSE2 offers new options for protection against HPSE1-mediated endothelial damage and preventing microvascular disease. © 2019, The Author(s)

Urokinase Receptor Counteracts Vascular Smooth Muscle Cell Functional Changes Induced by Surface Topography

© Ivyspring International Publisher. This is an open-access article distributed under the terms of the Creative Commons Licens

Laser printing of spherical silicon nanoparticles for in-plane color routing

Femtosecond laser printing allows the creation of spherical nanoparticles on a wide range of substrates. Here we apply this technique to fabricate Mie-resonant color-routing nanoantennas. First, we place single silicon particles on a dielectric multilayer and demonstrate color-selective directional excitation of Bloch surface waves. Second, we create asymmetric dimers of silicon nanospheres that provide color-selective directional scattering of evanescent waves. Our results highlight the potential of laser printing as an advanced fabrication technique for integrated optics