分类: 天文学 >> 天体物理学 提交时间: 2017-07-13
摘要: We carry out a systematical study of the spectral lag properties of 50 single-pulsed Gamma-Ray Bursts (GRBs) detected by Fermi/GBM. By dividing the light curves into multiple consecutive energy channels we provide a new measurement of the spectral lag which is independent on energy channel selections. We perform a detailed statistical study of our new measurements. We find two similar power-law energy dependencies of both the pulse arrival time and pulse width. Our new results on the power-law indices would favor the relativistic geometric effects for the origin of spectral lag. However, a complete theoretical framework that can fully account for the diverse energy dependencies of both arrival time and pulse width revealed in this work is still missing. We also study the spectral evolution behaviors of the GRB pulses. We find that the GRB pulse with negligible spectral lag would usually have a shorter pulse duration and would appear to have a ``hardness-intensity tracking'' (HIT) behavior and the GRB pulse with a significant spectral lag would usually have a longer pulse duration and would appear to have a ``hard-to-soft'' (HTS) behavior.
分类: 生物学 >> 生物物理学 提交时间: 2016-05-12
摘要: The phosphoinositide 3-kinase (PI3K)/protein kinase B (AKT) pathway has been identified as an important pathway in renal cell carcinoma (RCC). We have reported a nonsense mutation in PIK3R1, which encodes the regulatory subunit of PI3K, in a metastatic RCC (mRCC), while the mutation was absent in the corresponding primary RCC (pRCC). To identify the function of PIK3R1 in RCC, we examined its expression in normal kidney, pRCC and mRCC by immunohistochemistry and real-time polymerase chain reaction. The expression of PIK3R1 significantly decreased in pRCC and was further reduced in mRCC compared with normal tissue. Besides, its expression levels were negatively correlated with T-category of tumor stage. Additionally, 786-O and A-704 cells with PIK3R1 depletion introduced by CRISPR/Cas9 system displayed enhanced proliferation, migration and epithelial-mesenchymal transition (EMT), and acquired a stem-like phenotype. Moreover, the PIK3R1 depletion promoted the phosphorylation of AKT in the cells. The knockdown of AKT by shRNA reduced p-GSK3 beta and CTNNB1 expression in the cells, while the depletion of CTNNB1 impaired stem-like phenotype of the cells. Overall, PIK3R1 down-regulation in RCC promotes propagation, migration, EMT and stem-like phenotype in renal cancer cells through the AKT/GSK3 beta/CTNNB1 pathway, and may contribute to progression and metastasis of RCC.