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Stabilizing nanolasers via polarization lifetime tuning.

ABSTRACT: We investigate the emission dynamics of mutually coupled nanolasers and predict ways to optimize their stability, i.e., maximize their locking range. We find that tuning the cavity lifetime to the same order of magnitude as the dephasing time of the microscopic polarization yields optimal operation conditions, which allow for wider tuning ranges than usually observed in conventional semiconductor lasers. The lasers are modeled by Maxwell-Bloch type class-C equations. For our analysis, we analytically determine the steady state solutions, analyze the symmetries of the system and numerically characterize the emission dynamics via the underlying bifurcation structure. The polarization lifetime is found to be a crucial parameter, which impacts the observed dynamics in the parameter space spanned by frequency detuning, coupling strength and coupling phase.

SUBMITTER: Roos A

PROVIDER: S-EPMC8448855 | biostudies-literature | 2021 Sep

REPOSITORIES: biostudies-literature

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Stabilizing nanolasers via polarization lifetime tuning.

Roos Aycke A Meinecke Stefan S Lüdge Kathy K

Scientific reports 20210917 1

We investigate the emission dynamics of mutually coupled nanolasers and predict ways to optimize their stability, i.e., maximize their locking range. We find that tuning the cavity lifetime to the same order of magnitude as the dephasing time of the microscopic polarization yields optimal operation conditions, which allow for wider tuning ranges than usually observed in conventional semiconductor lasers. The lasers are modeled by Maxwell-Bloch type class-C equations. For our analysis, we analyti ...[more]

PMID: 34535698

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Project description:Glomerular podocytes are highly differentiated cells that are key components of the kidney filtration units. The podocyte cytoskeleton builds the basis for the dynamic podocyte cytoarchitecture and plays a central role for proper podocyte function. Recent studies implicate that immunosuppressive agents including the mTOR-inhibitor everolimus have a protective role directly on the stability of the podocyte cytoskeleton. To elucidate mechanisms underlying mTOR-inhibitor mediated cytoskeletal rearrangements, we carried out microarray gene expression studies to identify target genes and corresponding pathways in response to everolimus. We analyzed the effect of everolimus in a puromycin aminonucleoside experimental in vitro model of podocyte injury. Upon treatment with puromycin aminonucleoside, microarray analysis revealed gene clusters involving cytoskeletal-associated pathways, adhesion, migration and extracellular matrix composition to be affected. Everolimus is capable of protecting podocytes from injury, both on the transcriptome and protein level. Rescued genes included TUBB2B and DCDC2, both involved in microtubule structure formation in neuronal cells but not identified in podocytes so far. Confirming gene expression data, Western-blot analysis in cultured podocytes showed an increase of TUBB2B and DCDC2 protein after everolimus treatment, and immunohistochemistry in healthy control kidneys confirmed a podocyte-specific expression. Microtubule-inhibitor experiments led to a maldistribution of TUBB2B and DCDC2 as well as an aberrant reorganization of the actin cytoskeleton. Tubb2bbrdp/brdp mice showed a delay in glomerular podocyte and capillary development. Taken together, our study suggests that off-target, non-immune mediated effects of the mTOR-inhibitor everolimus on the podocyte cytoskeleton might involve regulation of microtubules, revealing a potential novel role of TUBB2B and DCDC2 in glomerular podocyte development We analyzed the effect of everolimus on gene expression in a puromycin aminonucleoside experimental in vitro model of podocyte injury using microarrays

Dataset Information

Stabilizing nanolasers via polarization lifetime tuning.

Publications

Stabilizing nanolasers via polarization lifetime tuning.

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