Increase of Pro-opiomelanocortin mRNA Prior to Tyrosinase, Tyrosinase-Related Protein 1, Dopachrome Tautomerase, Pmel-17/gp100, and P-Protein mRNA in Human Skin After Ultraviolet B Irradiation

In ultraviolet-induced tanning, the protein levels of various gene products critical for pigmentation (including tyrosinase and tyrosinase-related protein-1) are increased in response to ultraviolet B irradiation, but changes in mRNA levels of these factors have not been investigated in vivo. We have established an in situ hybridization technique to investigate mRNA levels of pro-opiomelanocortin, tyrosinase, tyrosinase-related protein-1, dopachrome tautomerase, P-protein, Pmel-17/gp100, and microphthalmia-associated transcription factor, and have analyzed the changes in mRNA levels in the ultraviolet B-exposed skin in vivo. The right or left forearm of each volunteer was irradiated with ultraviolet B, and skin biopsies were obtained at 2 and 5 d postirradiation. mRNA level of pro- opiomelanocortin was increased 2 d after ultraviolet B irradiation, and returned to a near-basal level after 5 d, whereas the mRNA levels of tyrosinase, tyrosinase-related protein-1, dopachrome tautomerase, P-protein, and Pmel-17/gp100 showed some or no increase at 2 d, but were significantly increased 5 d after ultraviolet B irradiation. Microphthalmia-associated transcription factor mRNA was slightly increased on days 2 and 5 after ultraviolet B irradiation. Our results suggest that the mechanism of the tanning response of human skin may involve the transcriptional regulation of certain pigmentary genes, and that pro-opiomelanocortin-derived melanocortins such as α-melanocyte-stimulating hormone and adrenocorticotropic hormone may play a part in regulating these genes in vivo

Expression and function of CCN2-derived circRNAs in chondrocytes

Cellular communication network factor 2 (CCN2) molecules promote endochondral ossification and articular cartilage regeneration, and circular RNAs (circRNAs), which arise from various genes and regulate gene expression by adsorbing miRNAs, are known to be synthesized from CCN2 in human vascular endothelial cells and other types of cells. However, in chondrocytes, not only the function but also the presence of CCN2-derived circRNA remains completely unknown. In the present study, we investigated the expression and function of CCN2-derived circRNAs in chondrocytes. Amplicons smaller than those from known CCN2-derived circRNAs were observed using RT-PCR analysis that could specifically amplify CCN2-derived circRNAs in human chondrocytic HCS-2/8 cells. The nucleotide sequences of the PCR products indicated novel circRNAs in the HCS-2/8 cells that were different from known CCN2-derived circRNAs. Moreover, the expression of several Ccn2-derived circRNAs in murine chondroblastic ATDC5 cells was confirmed and observed to change alongside chondrocytic differentiation. Next, one of these circRNAs was knocked down in HCS-2/8 cells to investigate the function of the human CCN2-derived circRNA. As a result, CCN2-derived circRNA knockdown significantly reduced the expression of aggrecan mRNA and proteoglycan synthesis. Our data suggest that CCN2-derived circRNAs are expressed in chondrocytes and play a role in chondrogenic differentiation

Safety and Pain-relief Efficacy of Urethral Catheter with Local-anesthetic Injection Port

Article信州医学雑誌 65(6): 355-359(2017)journal articl

Oxidative Modification to Cysteine Sulfonic Acid of Cys111 in Human Copper-Zinc Superoxide Dismutase

Copper-zinc superoxide dismutase (SOD1) plays a protective role against oxidative stress. On the other hand, recent studies suggest that SOD1 itself is a major target of oxidative damage and has its own pathogenicity in various neurodegenerative diseases, including familial amyotrophic lateral sclerosis. Only human and great ape SOD1s among mammals have the highly reactive free cysteine residue, Cys111, at the surface of the SOD1 molecule. The purpose of this study was to investigate the role of Cys111 in the oxidative damage of the SOD1 protein, by comparing the oxidative susceptibility of recombinant human SOD1 modified with 2-mercaptoethanol at Cys111 (2-ME-SOD1) to wild-type SOD1. Wild-type SOD1 was more sensitive to oxidation by hydrogen peroxide-generating fragments, oligomers, and charge isomers compared with 2-ME-SOD1. Moreover, wild-type SOD1, but not 2-ME-SOD1, generated an upper shifted band in reducing SDS-PAGE even by air oxidation. Using mass spectrometry and limited proteolysis, this upper band was identified as an oxidized subunit of SOD1; the sulfhydryl group (Cys-SH) of Cys111 was selectively oxidized to cysteine sulfinic acid (Cys-SO2H) and to cysteine sulfonic acid (Cys-SO3H). The antibody raised against a synthesized peptide containing Cys111-SO3H reacted with only the Cys111-peroxidized SOD1 by Western blot analysis and labeled Lewy bodylike hyaline inclusions and vacuole rims in the spinal cord of human SOD1-mutated amyotrophic lateral sclerosis mice by immunohistochemical analysis. These results suggest that Cys111 is a primary target for oxidative modification and plays an important role in oxidative damage to human SOD1, including familial amyotrophic lateral sclerosis mutants.This work was supported by Grants-in-aid for Scientific Research 17500242 and 19500313; a Hitech Research Center grant and the 21st Century Centers of Excellence program from the Ministry of Education, Culture, Sports, Science and Technology of Japan; and in part by a Grant for the Research Group on Development of Novel Therapeutics for ALS from the Ministry of Health, Labor and Welfare of Japan. The costs of publication of this article were defrayed in part by the payment of page charges. This article must therefore be hereby marked “advertisement” in accordance with 18 U.S.C. Section 1734 solely to indicate this fact

Early Results of a Wildfire Monitoring Microsatellite UNIFORM-1

UNIFORM (UNiversity International FORmation Mission) is a capacity building program in microsatellite field including satellites, ground stations, and data platform. The program, sponsored by the Ministry of Education, Culture, Sports and Technology (MEXT) of Japan, aims to increase the number of players in the small satellite community through education of both domestic and international young engineers, by providing them with an opportunity to study, build, and operate microsatellites. The first satellite of the program, UNIFORM-1 was launched on May 24th 2014. UNIFORM-1 is a 50-kg earth observation satellite whose mission is wildfiremonitoring using a microbolometer. Since then it has been in operation, successfully capturing several events on the ground including wildfires and volcanic activities. This paper presents in-orbit results of UNIFORM-1 mission, critical bus subsystems including EPS and AOCS, and lessons learned from its operations

CD Investigation of Porphyrin-Porphyrin Interaction with Links to Acyclic β-Sheet Peptide Self-Assembled in an Aqueous Media

Amphiphilic peptide, Ac-Cys(Por)-Lys-Val-(-Ser-Val-)n-Lys-Val-NH2 (n = 0 or 1, Cys(Por) = side-chain porphyrin-linked Cys), self-assembled to form the β-sheet in buffer solution-2,2,2-trifluoroethanol and showed exciton coupled Cotton effects in the porphyrin region due to the closely ori?ented porphyrin

Open MRI Operating Room with Automatic Electronic Recording of Medical Equipment Provided by Wireless LAN - Anesthesia Care Experience of ２５ Cases in Hiroshima University Hospital

オープンMRI設置手術室で25例の麻酔を経験した。MRI設置手術室では術中にMRI画像を判断材料として手術をすすめるため，MRI画像へのノイズ混入対策が必要である。また，MRI磁場の影響で術中にモニター機器や麻酔器が誤動作を起こす可能性があるため，MRI非対応機器からの画像ノイズの遮断対策として，電子機器から発生するノイズの軽減には特殊シールドボックスやイキソルメッシュを使用し，手術室外からのノイズには手術室全体にシールド工事を行った。MRIが発生させる磁場による電子機器の誤動作・故障対策は，オープンMRIの磁場が5ガウス以下となる範囲に電子機器や手術器具を置くことで対応した。問題の克服に加えて，医療機器からのデータの無線通信により，ケーブル類をなくすことでMRI撮影時の患者移動の簡素化をはかり，安全性を高めることができた。We provided anesthesia care for 25 patients in an open MRI operating room and summarized here our experience. When surgeons use MRI during surgery, the presence of noise in the images caused by other electronic equipment in the area often hinders accurate diagnosis.　In addition, malfunction of monitoring and anesthesia equipment during surgery due to the MRI magnetic field created during an MR examination can occur. In order to prevent imaging interference affecting equipment not compatible with MRI, we utilized 2 specially prepared shield boxes and wrapped the personal computer used for coordinating the data with a mesh-like cloth made by Ixol-mesh.　In addition, we prepared a shielded operating room in order to block noise from the outside. To prevent malfunction of the surgical and electronic instruments, we kept them outside the magnetic field of 5 Gauss or lower to minimize the magnetic effect generated with MRI.　Furthermore, patient safety during MRI imaging was improved by establishing a wireless communication system to feed data from medical devices, which allowed elimination of cabling