ORCID Profile
0000-0002-1334-887X
Current Organisation
University Of Strathclyde
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Publisher: The Endocrine Society
Date: 06-2016
DOI: 10.1210/EN.2016-1156
Abstract: The testicular vasculature forms a complex network, providing oxygenation, micronutrients, and waste clearance from the testis. The vasculature is also instrumental to testis function because it is both the route by which gonadotropins are delivered to the testis and by which T is transported away to target organs. Whether Sertoli cells play a role in regulating the testicular vasculature in postnatal life has never been unequivocally demonstrated. In this study we used models of acute Sertoli cell ablation and acute germ cell ablation to address whether Sertoli cells actively influence vascular structure and function in the adult testis. Our findings suggest that Sertoli cells play a key role in supporting the structure of the testicular vasculature. Ablating Sertoli cells (and germ cells) or germ cells alone results in a similar reduction in testis size, yet only the specific loss of Sertoli cells leads to a reduction in total intratesticular vascular volume, the number of vascular branches, and the numbers of small microvessels loss of germ cells alone has no effect on the testicular vasculature. These perturbations to the testicular vasculature leads to a reduction in fluid exchange between the vasculature and testicular interstitium, which reduces gonadotropin-stimulated circulating T concentrations, indicative of reduced Leydig cell stimulation and/or reduced secretion of T into the vasculature. These findings describe a new paradigm by which the transport of hormones and other factors into and out of the testis may be influenced by Sertoli cells and highlights these cells as potential targets for enhancing this endocrine relationship.
Publisher: AIP Publishing
Date: 19-09-2022
DOI: 10.1063/5.0114047
Abstract: Hybrid organic–inorganic perovskites have been widely studied in high-performance optoelectronic devices. Long-term stability is a key limitation to date in restricting their further development and commercial application. In general, interface properties between a semiconductor and an electrode highly affect device performance and stability. Herein, contact characteristics between the perovskite and electrode varying with illumination status have been first investigated. The results suggest that device's contact resistance (RC), obtained from a transfer length method, decreases as the incident light intensity increases. The RC under a higher irradiation intensity (1.26 mW/cm2) is about one-tenth of that at a lower density (0.08 mW/cm2). Simulation has been performed and shows a similar trend with experimental results. The interface physical model has been discussed based on an energy band theory. The band bending and barrier modulation at the interface under light illumination are originated from the surface states and the localized charges. This work explains the interface in determining device's fundamental properties, including stability, RC variation, and charge carrier transport process. It is significant in understanding the device working mechanism and providing a potential way for perovskite optoelectronic devices with enhanced stability and performance.
Publisher: Oxford University Press (OUP)
Date: 04-06-2014
DOI: 10.1093/CVR/CVU142
Publisher: Springer Science and Business Media LLC
Date: 20-04-2016
DOI: 10.1038/SREP24807
Abstract: Vascular calcification powerfully predicts mortality and morbidity from cardiovascular disease. Men have a greater risk of cardiovascular disease, compared to women of a similar age. These gender disparities suggest an influence of sex hormones. Testosterone is the primary and most well-recognised androgen in men. Therefore, we addressed the hypothesis that exogenous androgen treatment induces vascular calcification. Immunohistochemical analysis revealed expression of androgen receptor (AR) in the calcified media of human femoral artery tissue and calcified human valves. Furthermore, in vitro studies revealed increased phosphate (Pi)-induced mouse vascular smooth muscle cell (VSMC) calcification following either testosterone or dihydrotestosterone (DHT) treatment for 9 days. Testosterone and DHT treatment increased tissue non-specific alkaline phosphatase ( Alpl ) mRNA expression. Testosterone-induced calcification was blunted in VSMC-specific AR-ablated (SM-ARKO) VSMCs compared to WT. Consistent with these data, SM-ARKO VSMCs showed a reduction in Osterix mRNA expression. However, intriguingly, a counter-intuitive increase in Alpl was observed. These novel data demonstrate that androgens play a role in inducing vascular calcification through the AR. Androgen signalling may represent a novel potential therapeutic target for clinical intervention.
Publisher: Public Library of Science (PLoS)
Date: 09-05-2016
Publisher: AIP Publishing
Date: 07-11-2022
DOI: 10.1063/5.0098765
Abstract: The trade-off between mobility and stability in oxide thin-film transistors (TFTs) hinders further advances of an active-matrix flat panel display. Herein, a solution-processed bilayer active channel is designed to improve the stability and mobility simultaneously. The optical bandgap and work function of Tb:In2O3 films are modulated by tuning the film thickness and Tb concentration of Tb-doped indium oxide (Tb:In2O3) films. Large conduction band offset is achieved in a Tb:In2O3 bilayer channel, which induces accumulation of abundant electrons at the interface. The mobility is significantly improved to 38.2 cm2/V s, and the photoinduced stability of bilayer Tb:In2O3 TFTs is improved with low threshold voltage shift of 0.26 and −0.38 V under negative-bias illumination stress and negative-bias temperature illumination stress, respectively.
Location: United Kingdom of Great Britain and Northern Ireland
Location: United Kingdom of Great Britain and Northern Ireland
No related grants have been discovered for Junxi Wu.