The White Mountain Polarimeter Telescope and an Upper Limit on CMB Polarization

The White Mountain Polarimeter (WMPol) is a dedicated ground-based microwave telescope and receiver system for observing polarization of the Cosmic Microwave Background. WMPol is located at an altitude of 3880 meters on a plateau in the White Mountains of Eastern California, USA, at the Barcroft Facility of the University of California White Mountain Research Station. Presented here is a description of the instrument and the data collected during April through October 2004. We set an upper limit on $E$-mode polarization of 14 $\mu\mathrm{K}$ (95% confidence limit) in the multipole range $170<\ell<240$. This result was obtained with 422 hours of observations of a 3 $\mathrm{deg}^2$ sky area about the North Celestial Pole, using a 42 GHz polarimeter. This upper limit is consistent with $EE$ polarization predicted from a standard $\Lambda$-CDM concordance model.Comment: 35 pages. 12 figures. To appear in ApJ

Reactive Oxygen Species Hydrogen Peroxide Mediates Kaposi's Sarcoma-Associated Herpesvirus Reactivation from Latency

Kaposi's sarcoma-associated herpesvirus (KSHV) establishes a latent infection in the host following an acute infection. Reactivation from latency contributes to the development of KSHV-induced malignancies, which include Kaposi's sarcoma (KS), the most common cancer in untreated AIDS patients, primary effusion lymphoma and multicentric Castleman's disease. However, the physiological cues that trigger KSHV reactivation remain unclear. Here, we show that the reactive oxygen species (ROS) hydrogen peroxide (H2O2) induces KSHV reactivation from latency through both autocrine and paracrine signaling. Furthermore, KSHV spontaneous lytic replication, and KSHV reactivation from latency induced by oxidative stress, hypoxia, and proinflammatory and proangiogenic cytokines are mediated by H2O2. Mechanistically, H2O2 induction of KSHV reactivation depends on the activation of mitogen-activated protein kinase ERK1/2, JNK, and p38 pathways. Significantly, H2O2 scavengers N-acetyl-L-cysteine (NAC), catalase and glutathione inhibit KSHV lytic replication in culture. In a mouse model of KSHV-induced lymphoma, NAC effectively inhibits KSHV lytic replication and significantly prolongs the lifespan of the mice. These results directly relate KSHV reactivation to oxidative stress and inflammation, which are physiological hallmarks of KS patients. The discovery of this novel mechanism of KSHV reactivation indicates that antioxidants and anti-inflammation drugs could be promising preventive and therapeutic agents for effectively targeting KSHV replication and KSHV-related malignancies