Wiener-Hopf Analysis of the Diffraction by a Circular Waveguide Cavity

1.Introduction:The analysis of the scatteringand diffraction by open-ended metallic waveguide cavities has been of great interest recently in connection with the prediction and reduction of the radar cross section (RCS) of a target. This problem serves as a simple model of duct structures such as jet engine intakes of aircrafts and cracks occurringon surfaces of general complicated bodies. Therefore the investigation of a scattering mechanism in case of the existence of open cavities is an important subject in the field of the RCS prediction and reduction. Some of the cavity diffraction problems have been analyzed thus far usinga variety of different analytical and numerical methods. If the cavity dimensions are small in comparison to the incident wavelength, numerical techniques such as the method of moments and the finite element method can be applied efficiently. For large cavities with uniform cross sections, the results based on the waveguide modal approach by the use of the reciprocity relationship and the Kirchhoff approximation have been reported. In order to describe systematically the scattering mechanism as related to a fairly general class of large cavities with reasonable accuracy, the three ray-based approaches, namely, the method of shootingand bouncing rays, the Gaussian beam method, and the generalized ray expansion method have been developed. Furthermore, hybrid techniques such as the asymptotic/modal approach and the boundary integral/modal approach have also been established. These hybrid approaches take advantage of the efficiency of the modal analysis as well as the flexibility of asymptotic or numerical techniques. Most of these analysis methods incorporate the scatteringfrom the interior of the cavity includingthe rim diffraction at the open end, but they do not rigorously take into account the scattering effect arising from the entire exterior surface of the cavity. Therefore, final solutions due to these approaches are valid only for the restricted range of incidence and observation angles. In addition, these solutions may not be uniformly valid for arbitrary dimensions of the cavity.【査読有

Involvement of Laminin Binding Integrins and Laminin-5 in Branching Morphogenesis of the Ureteric Bud during Kidney Development

AbstractBranching morphogenesis of the ureteric bud (UB) [induced by the metanephric mesenchyme (MM)] is necessary for normal kidney development. The role of integrins in this complex developmental process is not well understood. However, the recent advent of in vitro model systems to study branching of UB cells and isolated UB tissue makes possible a more detailed analysis of the integrins involved. We detected integrin subunits α3, α6, β1, and β4 in both the UB and cells derived from the early UB. Blocking the function of each of these integrin subunits individually markedly inhibited branching morphogenesis in cell culture models. However, inhibiting individual integrin function with blocking antibodies in whole kidney and isolated UB culture only partially inhibited UB branching morphogenesis, suggesting that, in these more complex in vitro systems, multiple integrins are involved in the branching program. In whole organ and isolated bud culture, marked retardation of UB branching was observed only when both α3 and α6 integrin subunits were inhibited. The α6 integrin subunit can be expressed as both α6β1 and α6β4, and both of these β subunits are important for UB branching morphogenesis in both cell and organ culture. Furthermore, laminin-5, a common ligand for integrins α3β1 and α6β4, was detected in the developing UB and shown to be required for normal UB branching morphogenesis in whole embryonic kidney organ culture as well as isolated UB culture. Together, these data from UB cell culture, organ culture, and isolated UB culture models indicate that both integrin α3 and α6 subunits play a direct role in UB branching morphogenesis, as opposed to being modulators of the inductive effects of mesenchyme on UB development. Furthermore the data are consistent with a role for laminin-5, acting through its α3β1 and/or α6β4 integrin receptors, in UB branching during nephrogenesis. These data may help to partially explain the renal phenotype seen in integrin α3 and α3/α6 subunit-deficient animals

Citizen Science Observation of a Gamma‐Ray Glow Associated With the Initiation of a Lightning Flash

シチズンサイエンスで挑む雷の謎 --宇宙線と雷雲の相互作用は、雷の始まりに影響を与えるのか？--. 京都大学プレスリリース. 2023-07-10.Zeus also plays billiards: Citizen-supported Thundercloud Project may lead to better understanding of lightning's origins. 京都大学プレスリリース. 2023-07-12.Gamma-ray glows are observational evidence of relativistic electron acceleration due to the electric field in thunderclouds. However, it is yet to be understood whether such relativistic electrons contribute to the initiation of lightning discharges. To tackle this question, we started the citizen science “Thundercloud Project, ” where we map radiation measurements of glows from winter thunderclouds along Japan's sea coast area. We developed and deployed 58 compact gamma-ray monitors at the end of 2021. On 30 December 2021, five monitors simultaneously detected a glow with its radiation distribution horizontally extending for 2 km. The glow terminated coinciding with a lightning flash at 04:08:34 JST, which was recorded by the two radio-band lightning mapping systems, FALMA and DALMA. The initial discharges during the preliminary breakdown started above the glow, that is, in vicinity of the electron acceleration site. This result provides one example of possible connections between electron acceleration and lightning initiation

Chemosensitivity of radioresistant cells in the multicellular spheroids of A549 lung adenocarcinoma

<p>Abstract</p> <p>Background</p> <p>The relapse of cancer after radiotherapy is a clinical knotty problem. Previous studies have demonstrated that the elevation of several factors is likely in some way to lead to the development of treatment tolerance, so it is necessary to further explore the problem of re-proliferated radioresistant cells to chemotherapeutic agents. In the present study, we aimed to investigate the chemosensitivity of radioresistant cells originated from the multicellular spheroids of A549 lung adenocarcinoma.</p> <p>Methods</p> <p>After irradiated with 25 Gy of 6 MV X-ray to A549 multicellular spheroids, whose 10th re-proliferated generations were employed as radioresistant cells, and the control groups were A549 parental cells and MCF7/VCR resistant cells. The chemo-sensitivity test was made by six kinds of chemotherapeutic drugs which were DDP, VDS, 5-Fu, HCP, MMC and ADM respectively, while verapamil (VPL) was used as the reversal agent. Then the treatment effect was evaluated by MTT assay, and the multidrug resistant gene expressions of <it>mdr1 </it>and <it>MRP </it>were measured by RT-PCR.</p> <p>Results</p> <p>Both A549 parental cells and A549 derived radioresistant cells were resistant to DDP, but sensitive to VDS, 5-Fu, HCP, MMC and ADM. The inhibitory rates of VPL to these two types of cell were 98% and 25% respectively (P < 0.001). In addition, without drugs added, the absorbance value (A value) of A549 parental cells was 2-folds higher than that of their radioresistant cells (P < 0.001). As to the MCF7/VCR cells, they were resistant to DDP and VDS, but slight sensitive to MMC, ADM, 5-Fu, and HCP with 80% of inhibitory rate to VPL. The subsequent RT-PCR demonstrated that the <it>Mdr1</it>/β2-MG and <it>MRP</it>/β2-MG of all A549 cells were about 0 and 0.7 respectively, and those of MCF7/VCR cells were 35 and 4.36.</p> <p>Conclusion</p> <p>The chemosensitivity of A549 radioresistant cells had not changed markedly, and the decreased sensitivity to VPL could not be explained by the gene expression of <it>mdr1 </it>and <it>MRP</it>. It is possible that the changes in the cell membrane and decreased proliferate ability might be attributed to the resistance. Unlike multidrug resistance induced by chemotherapy, VPL may be not an ideal reverser to radioresistant cells. Therefore, the new biological strategy needs to be developed to treat recurring radioresistant tumor in combination with chemotherapy.</p

First experimental determination of the radiative-decay probability of the 31− state in ¹²C for estimating the triple alpha reaction rate in high temperature environments

The triple alpha reaction is one of the most important reactions in the nuclear astrophysics. However, its reaction rate in high temperature environments at T₉>2 was still uncertain. One of the major origins of the uncertainty was that the radiative-decay probability of the 3⁻₁ state in ¹²C was unknown. In the present work, we have determined the radiative-decay probability of the 3⁻₁ state to be 1.3[+1.2][-1.1] × 10⁻⁶ by measuring the ¹H(¹²C, ¹²Cp) reaction for the first time, and derived the triple alpha reaction rate in high temperature environments from the measured radiative-decay probability. The present result suggests that the 3⁻₁ state noticeably enhances the triple alpha reaction rate although the contribution from the 3⁻₁ state had been assumed to be small

Regulation of mammary gland branching morphogenesis by the extracellular matrix and its remodeling enzymes.

A considerable body of research indicates that mammary gland branching morphogenesis is dependent, in part, on the extracellular matrix (ECM), ECM-receptors, such as integrins and other ECM receptors, and ECM-degrading enzymes, including matrix metalloproteinases (MMPs) and their inhibitors, tissue inhibitors of metalloproteinases (TIMPs). There is some evidence that these ECM cues affect one or more of the following processes: cell survival, polarity, proliferation, differentiation, adhesion, and migration. Both three-dimensional culture models and genetic manipulations of the mouse mammary gland have been used to study the signaling pathways that affect these processes. However, the precise mechanisms of ECM-directed mammary morphogenesis are not well understood. Mammary morphogenesis involves epithelial 'invasion' of adipose tissue, a process akin to invasion by breast cancer cells, although the former is a highly regulated developmental process. How these morphogenic pathways are integrated in the normal gland and how they become dysregulated and subverted in the progression of breast cancer also remain largely unanswered questions