Study of the Equatorial and Low-Latitude Electrodynamic and Ionospheric Disturbances During the 22-23 June 2015 Geomagnetic Storm Using Ground-Based and Spaceborne Techniques.

We use a set of ground-based instruments (Global Positioning System receivers, ionosondes, magnetometers) along with data of multiple satellite missions (Swarm, C/NOFS, DMSP, GUVI) to analyze the equatorial and low-latitude electrodynamic and ionospheric disturbances caused by the geomagnetic storm of 22-23 June 2015, which is the second largest storm in the current solar cycle. Our results show that at the beginning of the storm, the equatorial electrojet (EEJ) and the equatorial zonal electric fields were largely impacted by the prompt penetration electric fields (PPEF). The PPEF were first directed eastward and caused significant ionospheric uplift and positive ionospheric storm on the dayside, and downward drift on the nightside. Furthermore, about 45 min after the storm commencement, the interplanetary magnetic field (IMF) Bz component turned northward, leading to the EEJ changing sign to westward, and to overall decrease of the vertical total electron content (VTEC) and electron density on the dayside. At the end of the main phase of the storm, and with the second long-term IMF Bz southward turn, we observed several oscillations of the EEJ, which led us to conclude that at this stage of the storm, the disturbance dynamo effect was already in effect, competing with the PPEF and reducing it. Our analysis showed no significant upward or downward plasma motion during this period of time; however, the electron density and the VTEC drastically increased on the dayside (over the Asian region). We show that this second positive storm was largely influenced by the disturbed thermospheric conditions.

Expression of Thy-1 on rat T cells and its relevance as a maturation marker of T cells in rats.

Expression of Thy-1 and CD3 antigens on thymocytes and the nylon wool-non-adherent (nylon-nonad) fractions of peripheral lymphocytes in F344 rats was studied by flow cytometry using anti-Thy-1 and anti-CD3 antibodies. In terms of the expression and density of Thy-1 and CD3, the thymus and peripheral lymphoid tissues in rats contained different populations. Nearly all thymocytes showed a high density of Thy-1 (Thy-1hi); a small population with a low density of Thy-1 (Thy-1lo) was found in CD3 bright-positive (CD3hi) thymocytes. Three-color analysis with CD4, CD8 and Thy-1 revealed Thy-1lo thymocytes to have mainly CD4 or CD8; Thy-1hi thymocytes also contained CD4 or CD8 single-positive (SP) cells as a minor population. Thus, SP thymocytes bearing CD3 were divided into two populations by evaluation of the density of Thy-1. Of peripheral CD3+ T cells, 15% showed a low density of Thy-1+ and the others were Thy-1-. Both T cells responded to anti-CD3 monoclonal antibody (mAb). However, no Thy-1hi T cells were found in peripheral lymphoid tissues. These results suggested that SP thymocytes in rats develop with the reduction of Thy-1, but not with its loss, and are newly supplied to peripheral lymphoid tissues as the phenotype, Thy-1lo, and are altered to Thy-1- T cells. Analysis of each cell size and disappearance of peripheral Thy-1lo T cells with age supported the above conclusion.(ABSTRACT TRUNCATED AT 250 WORDS)

Characterization of the T cells in aged rat bone marrow.

In this study, we determined the characteristics of CD3-positive (CD3+) T cells existing in rat bone marrow (BM). In contrast to splenic T cells, BM CD3+ T cells are composed of a higher proportion of CD8+ T cells, and the number of both cell types increased with age. Such CD3+ T cells in aged rats showed a similar usage of TCR V beta as splenic T cells, suggesting that BM CD3+ T cells are thymus-dependent and composed of an ordinary population in view of the expression of the TCR beta-chain. Purified T cells obtained from aged rat BM showed a markedly proliferative response by stimulation with immobilized anti-CD3 mAb, as did splenic T cells. However, the addition of BM non-T cells completely inhibited the response of both BM and splenic T cells in vitro. These results suggest that T cells in rat BM are negatively regulated by BM non-T cells in their response to the TCR-mediated signal not to disrupt the microenvironment of the BM.

Establishment of efficient reaggregation culture system for gene transfection into immature T cells by retroviral vectors.

To overcome low efficiency of retroviral infection into immature T cells, we modified reaggregation fetal thymus organ culture by closely packed co-culture with virus-producing cells (VPC). The viral vector was constructed in chimeric vector, pMX, with IRES and tailless-rat CD2 as a surface marker of infected cells. A rearranged TCR beta gene (Vbeta8.2) was further inserted into the construct for investigating effect of the introduced gene in T cell development. Using this system, we succeeded to transfer the viral vector into immature thymocytes at a remarkably higher efficiency compared to conventional methods using medium containing retrovirus. Moreover, the introduced TCR beta gene was expressed on thymocytes of RAG2-deficient mice to induce in the transition of CD4-CD8- double-negative (DN) into CD4+CD8+ double-positive (DP) cells by transducing beta-selection signaling. Thus, our modified reaggregation culture system is useful for studying the molecular mechanism of T cell development due to a highly efficient gene transfer into immature T cells.

Pre-Kupffer like CD4/CD8 double positive mononuclear cells present in rat liver.

Nonparenchymal cells isolated from Fischer rat liver were separated into subpopulations by passage through a nylon wool column and/or culturing in a plastic plate. Besides typical Kupffer cells, we detected a unique population of cells (called PKu cells) which were plastic adherent but did not spread on a short term culture, were nonadherent on nylon wool, and were nonphagocytic, as opposed to Kupffer cells. Both Kupffer cells and PKu cells expressed CD4 (recognized with W3/25 mAb), CD8 (OX-8), a NK cell antigen (3.2.3), and a monocyte antigen (OX-41), as assessed by flow cytofluorometry. However, the proportion of cells bearing high densities of CD8 and 3.2.3 antigens was much larger for PKu cells than for Kupffer cells. Reverse transcriptase-PCR analysis of CD8 mRNA revealed that PKu cells expressed the CD8 alpha chain but not the beta chain. When PKu cells were treated with phorbol 12-myristate 13-acetate (PMA), they exhibited spreading and phagocytic activities, and showed a similar morphology to Kupffer cells in the spread form. Moreover, PMA treatment decreased the high density of CD8 antigen on PKu cells. These findings indicated that PKu cells present in normal rat liver are precursors of Kupffer cells.

Conformation of nucleoplasmin and its interaction with DNA-protamine complex as a simple model of fish sperm nuclei.

Nucleoplasmin was isolated from Xenopus laevis eggs and purified by an improved method using an open column. Its conformation was investigated spectrophotometrically by UV, CD and fluorescence. It was shown that alpha-helix content of nucleoplasmin was 30-40%, and one of the two tryptophan residues in nucleoplasmin located in the hydrophobic surroundings and the other in the relatively hydrophilic surroundings. The isolated nucleoplasmin was found to decondense sperm nuclei of salmon also, suggesting a possibility of the existence of nucleoplasmin-like protein in fish as well. Collapse of the protamine (salmine)-DNA complex as a simple model for fish sperm nuclei by nucleoplasmin was directly observed by measuring OD320 of aqueous protamine-DNA mixtures. This is a molecular level observation for the removal of protamine from DNA-protamine complex.

Mechanism of salmon sperm decondensation by nucleoplasmin.

Removal of protamine from DNA-protamine (salmine, protamine from salmon sperm) complexes by nucleoplasmin was examined and compared with that of poly-L-glutamic acid (PLGA) using turbidity and ethidium bromide (EB) treatment methods. When nucleoplasmin or PLGA was added to a DNA-protamine complex solution, turbidity was decreased and the amount of EB intercalated into DNA was increased. These results suggest that nucleoplasmin and PLGA can remove protamine from DNA-protamine complexes. The effect of nucleoplasmin was more potent than that of PLGA. Direct interaction of nucleoplasmin with protamine was confirmed by mixing experiments using circular dichroism (CD) and fluorescence spectroscopies. Results suggest that nucleoplasmin is bound to protamine in a 1:1 ratio and that Trp126 is located near a hydrophilic region containing a polyglutamic acid tract of nucleoplasmin which was obviously influenced by its binding with protamine. It would appear that the polyglutamic acid tract in nucleoplasmin plays a critical role for binding with protamine.

Measurements of radionuclides induced in the accelerator structure of the KEK-PS.

Radionuclides induced in accelerator structures were measured during each long shut-down by using a pure Ge detector and a portable multichannel pulse height analyzer. Variation in the nuclide composition for various points in the accelerator tunnel was investigated. The decay of the exposure rate was calculated using the measured nuclide composition. Radionuclide measurements of the vacuum chamber removed from the accelerator were also performed. The relation between the variation of the residual exposure rate and that of the nuclide composition was examined and it was found that the proportion of 48V, 54Mn and 56Co corresponds to variation in the beam loss pattern.