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We demonstrate polarization-independent resonant-enhancement of second harmonic generation (SHG) from multilayer Gallium Selenide (GaSe) on a silicon-based resonant metasurface. Two-dimensional hexagonal photonic lattice with circularly symmetric silicon meta-atoms are designed to achieve resonant field enhancement at the fundamental wavelength independent of the incident polarization direction. Such structures are however found to exhibit strong resonant field depolarization effects at the fundamental excitation fields resulting in modified nonlinear polarization components when compared to the native GaSe layer. Furthermore, the sub-wavelength metasurface designed to have resonances at the fundamental wavelengths act as a higher order diffraction grating at the second harmonic wavelength. Nonlinear wave propagation simulations show that the higher order diffracted SHG exhibit strong polarization dependent enhancement with characteristics very different from the native GaSe layer. In this context, polarization independent enhancement of the second harmonic signal is achieved only for the zeroth order diffracted component. Experimental study of second harmonic generation from the GaSe layer integrated with the silicon metasurface shows maximum nonlinear signal enhancement on-resonance with polarization dependence identical to the native GaSe layer by selectively detecting the zeroth-order diffracted component. This work shows that it is not sufficient to use symmetric meta-atoms in such 2D material integrated resonant metasurfaces for achieving polarization independent nonlinear optical enhancement. Depolarization of the resonant fields and higher-order diffraction at the nonlinear signal wavelength need to be considered as well.

Collagen I, the most abundant extracellular matrix (ECM) protein in vertebrate tissues provides mechanical durability to tissue microenvironments and regulates cell function. Its fibrillogenesis in biological milieu is predominantly regulated by dermatan sulfate proteoglycans, proteins conjugated with iduronic acid-containing dermatan sulfate (DS) glycosaminoglycans (GAG). Although DS is known to regulate tissue function through its modulation of Coll I architecture, a precise understanding of the latter remains elusive. We investigated this problem by visualizing the fibrillar pattern of fixed Coll I gels polymerized in the presence of varying concentrations of DS using second harmonic generation microscopy. Measuring mean second harmonic generation signal (which estimates the ordering of the fibrils), and surface occupancy (which estimates the space occupied by fibrils) supported by confocal reflectance microscopy, our observations indicated that the effect on fibril pattern of DS is contextual upon the latter's concentrations: Lower levels of DS resulted in sparse disorganized fibrils; higher levels restore organization, with fibrils occupying greater space.An appropriate change in elasticity as a result of DS levels was also observed through atomic force microscopy. Examination of dye-based GAG staining and scanning electron microscopy suggested distinct constitutions of Coll I gels when polymerized with higher and lower levels of DS. We observed that adhesion of the invasive ovarian cancer cells SKOV3 decreased for lower DS levels but was partially restored at higher DS levels. Our study shows how the Coll I gel pattern-tuning of DS is of relevance for understanding its biomaterial applications and possibly, pathophysiological functions.

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Faithful mimics of tuberculosis (TB) infection are warranted needed to providefor mechanistic insights into the complex host-pathogen interactions and for accelerating drug discovery. The current in vitro models provide a short duration to investigate the biology of this slow-growing pathogen, present divergent transcriptional signatures to human infections, and are unreliable drug discovery platforms. We developed and characterized a 3D collagen culture system mimicking the lung microenvironment (collagen fibres, pore size and stiffness), where we incorporated Mycobacterium tuberculosis (Mtb) infected THP-1 or primary monocytes. Dual RNA-sequencing revealed high similarity with human infections. Phenotypes observed in humans infection, such as foamy macrophages and mycobacterial cords (never seen in any other in vitro culture system), were reproduced in our culture system. The system overcomes many challenges associated with the traditional platforms for studying Mtb infections, including showing remarkable efficacy with clinically relevant concentrations of first-line anti-TB drug pyrazinamide, not seen in any other in vitro model, making it reliable, readily adoptable for tuberculosis studies and drug screening.