The dynamics of inter-Sertoli (SC) tight junctions (TJ) are regulated by transforming growth factor-beta 3 (TGF-beta 3) via the p38 mitogen-activated protein (MAP) kinase signaling pathway

published_or_final_versio

The thermal response of A pulsar glitch: The nonspherically symmetric case

We study the thermal evolution of a pulsar after a glitch in which the energy is released from a relatively compact region. A set of relativistic thermal transport and energy balance equations is used to study the thermal evolution, without making the assumption of spherical symmetry. We use an exact cooling model to solve this set of differential equations. Our results could differ significantly from those obtained under the assumption of spherical symmetry. Even for young pulsars with a hot core like the Vela pulsar, a detectable hot spot could be observed after a glitch if a large amount of energy is released in a small region close to the surface of the star. The results suggest that the intensity variation and the relative phases of hard X-ray emissions in different epochs may provide important information on the equation of state. © 1998. The American Astronomical Society. All rights reserved.published_or_final_versio

Cytokines and junction restructuring during spermatogenesis - A lesson to learn from the testis

In the mammalian testis, preleptotene and leptotene spermatocytes residing in the basal compartment of the seminiferous epithelium must traverse the blood-testis barrier (BTB) at late stage VIII through early stage IX of the epithelial cycle during spermatogenesis, entering the adluminal compartment for further development. However, until recently the regulatory mechanisms that regulate BTB dynamics remained largely unknown. We provide a critical review regarding the significance of cytokines in regulating the 'opening' and 'closing' of the BTB. We also discuss how cytokines may be working in concert with adaptors that selectively govern the downstream signaling pathways. This process, in turn, regulates the dynamics of either Sertoli-Sertoli tight junction (TJ), Sertoli-germ cell adherens junction (AJ), or both junction types in the epithelium, thereby permitting TJ opening without compromising AJs, and vice versa. We also discuss how adaptors alter their protein-protein association with the integral membrane proteins at the cell-cell interface via changes in their phosphorylation status, thereby altering adhesion function at AJ. These findings illustrate that the testis is a novel in vivo model to study the biology of junction restructuring. Furthermore, a molecular model is presented regarding how cytokines selectively regulate TJ/AJ restructuring in the epithelium during spermatogenesis. © 2005 Elsevier Ltd. All rights reserved.postprin

Differential interactions between transforming growth factor-β3/ TβR1, TAB1, and CD2AP disrupt blood-testis barrier and sertoli-germ cell adhesion

The biochemical basis that regulates the timely and selective opening of the blood-testis barrier (BTB) to migrating preleptotene/leptotene spermatocytes at stage VIII of the epithelial cycle in adult rat testes is virtually unknown. Recent studies have shown that cytokines (e.g. transforming growth factor (TGF)-β3) may play a crucial role in this event. However, much of this information relies on the use of toxicants (e.g. CdCl 2), making it difficult to relay these findings to normal testicular physiology. Here we report that overexpression of TGF-β3 in primary Sertoli cells cultured in vitro indeed perturbed the tight junction (TJ) barrier with a concomitant decline in the production of BTB constituent proteins as follows: occludin, N-cadherin, and ZO-1. Additionally, local administration of TGF-β3 to testes in vivo was shown to reversibly perturb the BTB integrity and Sertoli-germ cell adhesion via the p38 MAPK and ERK signaling pathways. Most importantly, the simultaneous activation of p38 and ERK signaling pathways is dependent on the association of the TGF-β3-TβR1 complex with adaptors TAB1 and CD2AP because if TβR1 was associated preferentially with CD2AP, only Sertoli-germ cell adhesion was perturbed without compromising the BTB. Collectively, these data illustrate that local production of TGF-β3, and perhaps other TGF-βs and cytokines, by Sertoli and germ cells into the microenvironment at the BTB during spermatogenesis transiently perturbs the BTB and Sertoli-germ cell adhesion to facilitate germ cell migration when the activated TβRI interacts with adaptors TAB1 and CD2AP. However, TGF-β3 selectively disrupts Sertoli-germ cell adhesion in the seminiferous epithelium to facilitate germ cell migration without compromising BTB when TβRI interacts only with adaptor CD2AP. © 2006 by The American Society for Biochemistry and Molecular Biology, Inc.postprin

Induction of collagen expression during inter-sertoli Tight Junction (TJ) assembly in vitro

published_or_final_versio

Correlation between hot-carrier-induced interface states and GIDL current increase in N-MOSFET's

Correlation between created interface states and GIDL current increase in n-MOSFET's during hot-carrier stress is quantitatively discussed. A trap-assisted two-step tunneling model is used to relate the increased interface-state density (ADH) with the shift in GIDL current (ΔI d). Results show that under appropriate drain-gate biases, the two-step tunneling is so dominant that A/d is insensitive to temperatures up to about 50 °C. With the help of 2-D device simulation, the locations of the drain region with significant two-step tunneling and the energy levels of the traps involved can be found, with both depending on the drain voltage. From these insights on ADit,A/d and their relation, A Du near the midgap can be estimated, with an error less than 10% as compared to the results of chargepumping measurement on the same transistors. Devices with nitrided gate oxide, different gate-oxide thicknesses and different channel dimensions are also tested to verify the above correlation. © 1998 IEEE.published_or_final_versio

Probabilistic optimal sizing of stand-alone PV systems with modeling of variable solar radiation and load demand

PSPI Committee Main/Planning for Integration of Renewable Resources, DGs, and EVs into the Electric Grid (combo): presentation no. 2012GM0675This paper presents a comprehensive sizing methodology which could contain all key elements necessary to obtain a practical sizing result for a stand-alone photovoltaic (PV) system. First, a stochastic solar radiation model based on limited/incomplete local weather data is formulated to synthesis various chronological solar radiation patterns. This enables us to evaluate a long-term system performance and characterize any extreme weather conditions. Second, a stochastic load simulator is developed to simulate realistic load patterns. Third, two reliability indices, Expected-Energy-Not-Supplied (EENS) and Expected-Excessive-Energy-Supplied (EEES), are incorporated with an Annualized Cost of System (ACS) to form a new objective function called an Annualized Reliability and Cost of System (ARCS) for optimization. We then apply a particle swarm optimization (PSO) algorithm to obtain the optimum system configuration for a given acceptable risk level. An actual case study is conducted to demonstrate the feasibility and applicability of the proposed methodology. © 2012 IEEE.published_or_final_versionThe 2012 IEEE Power and Energy Society General Meeting, San Diego, CA., 22-26 July 2012. In IEEE Power and Energy Society General Meeting Proceedings, 2012, p. 1-

Disruption of Sertoli-germ cell adhesion function in the seminiferous epithelium of the rat testis can be limited to adherens junctions without affecting the blood-testis barrier integrity: An in vivo study using an androgen suppression model

During spermatogenesis, both adherens junctions (AJ) (such as ectoplasmic specialization (ES), a testis-specific AJ type at the Sertoli cell-spermatid interface (apical ES) or Sertoli-Sertoli cell interface (basal ES) in the apical compartment and BTB, respectively) and tight junctions (TJ) undergo extensive restructuring to permit germ cells to move across the blood-testis barrier (BTB) as well as the seminiferous epithelium from the basal compartment to the luminal edge to permit fully developed spermatids (spermatozoa) to be sloughed at spermiation. However, the integrity of the BTB cannot be compromised throughout spermatogenesis so that postmeiotic germ cell-specific antigens can be sequestered from the systemic circulation at all times. We thus hypothesize that AJ disruption in the seminiferous epithelium unlike other epithelia, can occur without compromising the BTB-barrier, even though these junctions, namely TJ and basal ES, co-exist side-by-side in the BTB. Using an intratesticular androgen suppression-induced germ cell loss model, we have shown that the disruption of AJs indeed was limited to the Sertoli-germ cell interface without perturbing the BTB. The testis apparently is using a unique physiological mechanism to induce the production of both TJ- and AJ-integral membrane proteins and their associated adaptors to maintain BTB integrity yet permitting a transient loss of cell adhesion function by dissociating N-cadherin from β-catenin at the apical and basal ES. The enhanced production of TJ proteins, such as occludin and ZO-1, at the BTB site can supersede the transient loss of cadherin-catenin function at the basal ES. This thus allows germ cell depletion from the epithelium without compromising BTB integrity. It is plausible that the testis is using this novel mechanism to facilitate the movement of preleptotene and leptotene spermatocytes across the BTB at late stage VIII through early stage IX of the epithelial cycle in the rat while maintaining the BTB immunological barrier function. © 2005 Wiley-Liss, Inc.postprin

Extracellular matrix (ECM) regulates the dynamics of tight junctions (TJs) in the testis possibly via its interactions with cytokines and proteases

Abstract no. 646published_or_final_versio

The localization of multiple cathepsin mRNAs in the seminiferous epithelium by in situ hybridization is consistent with their role in germ cell (GC) migration

Abstract no. 707published_or_final_versio