分类： 地球科学 >> 空间物理学 提交时间： 2016-05-12
摘要： We present high-resolution observations of a quiescent solar prominence that consists of a vertical and a horizontal foot encircled by an overlying spine and has ubiquitous counter-streaming mass flows. While the horizontal foot and the spine were connected to the solar surface, the vertical foot was suspended above the solar surface and was supported by a semicircular bubble structure. The bubble first collapsed, then reformed at a similar height, and finally started to oscillate for a long time. We find that the collapse and oscillation of the bubble boundary were tightly associated with a flare-like feature located at the bottom of the bubble. Based on the observational results, we propose that the prominence should be composed of an overlying horizontal spine encircling a low-lying horizontal and vertical foot, in which the horizontal foot consists of shorter field lines running partially along the spine and has ends connected to the solar surface, while the vertical foot consists of piling-up dips due to the sagging of the spine fields and is supported by a bipolar magnetic system formed by parasitic polarities (i.e., the bubble). The upflows in the vertical foot were possibly caused by the magnetic reconnection at the separator between the bubble and the overlying dips, which intruded into the persistent downflow field and formed the picture of counter-streaming mass flows. In addition, the counter-streaming flows in the horizontal foot were possibly caused by the imbalanced pressure at the both ends.
分类： 生物学 >> 生物物理学 提交时间： 2016-05-11
Ye, Lei
Li, Wuping
Liu, Zhong
Ye, Lei
Li, Wuping
Liu, Zhong
Yu, Haisheng
Zhang, Liguo
Li, Chengwen
Hirsch, Matthew L.
Samulski, R. Jude
Li, Wuping
摘要： Liver cirrhosis and hepatocellular carcinomas are major health problems of chronic hepatitis B virus (HBV) infection. To date, rare model has reproduced liver fibrosis associated with long-term HBV infection which in turn has hindered both the understanding of HBV biology and the development of new treatment options. Here, using adeno-associated virus serotype 8 (AAV8) mediated delivery of a 1.2-kb HBV genome, we successfully generated a chronic HBV infectious mouse model that presents the associated liver fibrosis observed following human infection. After AAV8/HBV1.2 vector administration, mice demonstrated effective HBV replication and transcription which resulted in HBV antigen expression and viremia over 6 months. Although no obvious acute inflammatory response was noted, these mice still developed chronic liver disease and hepatic fibrogenesis as demonstrated by increased ground glass-like hepatocytes, an increasing trend of collagen deposition and upregulated fibrosis markers, including type I collagen, type III collagen, tissue inhibitor of metalloproteinase (TIMP), and transforming growth factor-beta 1(TGF-beta 1). Taken together, AAV-mediated HBV gene delivery to the mouse liver, induced HBV persistent infection accompanied by liver fibrosis which can serve as a model for investigating the precise mechanisms underlying liver fibrosis following chronic HBV infection as well as for the potential development of novel therapeutics.
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