From Text to Sign Language: Exploiting the Spatial and Motioning Dimension

PACLIC 19 / Taipei, taiwan / December 1-3, 200

Fabrication of Microstructure Array using the Projection Microstereolithography System

Microstereolithography technology is similar to the conventional stereolithography process and enables to fabricate a complex 3D microstructure. This is divided into scanning and projection type according to aiming at precision and fabrication speed. The scanning MSL fabricates each layer using position control of laser spot on the resin surface, whereas the projection MSL fabricates one layer with one exposure using a mask. In the projection MSL, DMD used to generate dynamic pattern consists of micromirrors which have per side. The fabrication range and resolution are determined by the field of view of the DMD and the magnification of the projection lens. If using the projection lens with high power, very fine microstructures can be fabricated. In this paper, the projection MSL system adapted to a large surface for array-type fabrication is presented. This system covers the meso range, which is defined as the intermediate range between micro and macro, with a resolution of a few . The fabrication of array-type microstructures has been demonstrated to verify the performance of implemented system

Distribution and Kinematics of H I through Raman He II Spectroscopy of NGC 6302

The young planetary nebula NGC 6302 is known to exhibit Raman-scattered He II features at 6545 and 4851 Angstrom. These features are formed through inelastic scattering of He II$\lambda\lambda$ 1025 and 972 with hydrogen atoms in the ground state, for which the cross sections are $1.2 \times 10^{-21}$ and $1.4\times 10^{-22} {\rm\ cm^2}$, respectively. We investigate the spectrum of NGC 6302 archived in the ESO Science Portal. Our Gaussian line fitting analysis shows that the Raman-scattered He II features are broader and more redshifted than the hypothetical model Raman features that would be formed in a cold static H I medium. We adopt a simple scattering geometry consisting of a compact He II emission region surrounded by a H I medium to perform Monte Carlo simulations using the radiative transfer code ${\it STaRS}$. Our simulations show that the H I region is characterized by the H I column density $N_{\rm HI}=3\times 10^{21}{\rm\ cm^{-2}}$ with the random speed component $v_{\rm ran}=10{\rm\ km\ s^{-1}}$ expanding with a speed $v_{\rm exp}= 13{\rm\ km\ s^{-1}}$from the He II emission region. Based on our best fit parameters, we estimate the H I mass of the neutral medium$M_{\rm HI} \simeq 1.0\times 10^{-2}\ {\rm M_\odot}$, pointing out the usefulness of Raman He II spectroscopy as a tool to trace H I components.Comment: 12 pages, 8 figures, accepted for publication in Ap

3D Cell Printed Tissue Analogues: A New Platform for Theranostics

Stem cell theranostics has received much attention for noninvasively monitoring and tracing transplanted therapeutic stem cells through imaging agents and imaging modalities. Despite the excellent regenerative capability of stem cells, their efficacy has been limited due to low cellular retention, low survival rate, and low engraftment after implantation. Three-dimensional (3D) cell printing provides stem cells with the similar architecture and microenvironment of the native tissue and facilitates the generation of a 3D tissue-like construct that exhibits remarkable regenerative capacity and functionality as well as enhanced cell viability. Thus, 3D cell printing can overcome the current concerns of stem cell therapy by delivering the 3D construct to the damaged site. Despite the advantages of 3D cell printing, the in vivo and in vitro tracking and monitoring of the performance of 3D cell printed tissue in a noninvasive and real-time manner have not been thoroughly studied. In this review, we explore the recent progress in 3D cell technology and its applications. Finally, we investigate their potential limitations and suggest future perspectives on 3D cell printing and stem cell theranostics.116Nsciescopu

Increased expression of cysteine cathepsins in ovarian tissue from chickens with ovarian cancer

<p>Abstract</p> <p>Background</p> <p>Cysteine cathepsins (CTSs) are involved in the degradation and remodeling of the extracellular matrix and are associated with cell transformation, differentiation, motility, and adhesion. These functions are also related to cancer cell invasion and metastasis. Chickens spontaneously develop epithelial ovarian cancer and are therefore a good animal model for human ovarian cancer. However, no studies have investigated the expression of CTSs in chickens with ovarian cancer.</p> <p>Methods</p> <p>Cancerous (n = 5) and normal (n = 3) ovaries were collected from 2-to 3-year-old hens, and ovarian tissue samples were collected for study. Ovarian cancers were evaluated with hematoxylin and eosin staining. Reverse transcriptase and quantitative PCR analyses, in situ hybridization analysis were performed to examine the mRNA expression pattern of three CTSs in detail, and protein expression of CTSB was evaluated.</p> <p>Results</p> <p>The CTSB, CTSC, and CTSS genes were highly expressed in cancerous chicken ovaries. Messenger RNAs for the three CTSs were localized to a nodule area, a major characteristic of cancerous ovaries, but the three CTSs showed no specific localization in normal ovaries. Immunoreactive CTSB protein was present in the nodule area of cancerous ovaries.</p> <p>Conclusion</p> <p>Our results suggest that CTSB, CTSC, and CTSS have important functions in the development of epithelial ovarian cancer.</p