38 research outputs found
Generation of integration-free neural progenitor cells from cells in human urine
Human neural stem cells hold great promise for research and therapy in neural disease. We describe the generation of integration-free and expandable human neural progenitor cells (NPCs). We combined an episomal system to deliver reprogramming factors with a chemically defined culture medium to reprogram epithelial-like cells from human urine into NPCs (hUiNPCs). These transgene-free hUiNPCs can self-renew and can differentiate into multiple functional neuronal subtypes and glial cells in vitro. Although functional in vivo analysis is still needed, we report that the cells survive and differentiate upon transplant into newborn rat brain.postprin
Sex differences in the development of angiotensin II-induced hypertension in conscious mice
Sex differences in angiotensin II- and aldosterone-induced hypertension: the central protective effects of estrogen
Estrogen receptor-α mediates estrogen protection from angiotensin II-induced hypertension in conscious female mice
Sex differences in maternal gestational hypertension-induced sensitization of angiotensin II hypertension in rat offspring: the protective effect of estrogen
Role of the area postrema in angiotensin II modulation of baroreflex control of heart rate in conscious mice
Pore structure and free gas transport characteristics of deep shale: taking Longmaxi Formation shale in Sichuan Basin as an example
Deep shale gas is an important research direction for increasing shale gas storage and production in the Longmaxi Formation of Sichuan Basin. But there are differences in reservoir and seepage characteristics between shallow and medium-buried shale gas, which to some extent limits the progress of exploration and development of deep shale gas. In order to clarify the pore structure characteristics of deep shale gas reservoirs and the transport characteristics of shale free gas, this paper takes the high-quality shale of Longmaxi Formation in southern Sichuan as an example to carry out experiments on observing and quantitatively characterizing the pore structure of shale reservoirs. In addition, based on the transport mechanism of bulk gas, the transport characteristics, critical conditions, and dynamic evolution laws of shale free gas were explored. The experimental and computational results indicate that: (1) The pore morphology characteristics of deep shale reservoirs are not significantly different from those of shallow and medium-buried shale, but the pore structure characteristics of medium pores are more obvious, with pore volume accounting for 62.5%-69.7%; (2) The transport modes of deep shale free gas are divided into three types: transitional flow, slippage flow, and Darcy flow. The critical pore sizes of the three modes in the Yongchuan area are 4.2 nm and 420 nm, respectively. On this basis, a transport chart for free gas in the entire basin has been established; (3) From shallow to deep shale, the critical pore size corresponding to different transport modes of free gas decreases accordingly. The main transport mode of free gas changes from the transitional flow (up to 63.0%) to the slippage flow (up to 67.3%) and the Darcy flow accounts for no more than 2%. The transport capacity of free gas rapidly decreases from shallow to medium-buried shale, while the transport capacity of medium to deep shale free gas remains basically stable with increasing burial depth. By analyzing and comparing the pore structure characteristics and free gas transport characteristics of deep and shallow shale reservoirs, this study can effectively support the deployment of efficient exploration and development plans for deep shale gas and even shallow shale gas in the next step
Establishment of an ectodermal dysplasia related gene EDA Knockout human embryonic stem cell line (WAe001-A-22) by CRISPR-Cas9 technology
EDA is a gene located at Xq13.1. It encodes different isoforms of tumor necrosis factor (TNF) superfamily member ectodysplasin A. Ectodysplasin A is a transmembrane protein which can be cleaved to form a secreted form and interact with EDA receptor to mediate the development of ectoderm. Mutations of the EDA gene are related to ectodermal dysplasia and tooth agenesis. Here, we report the establishment of the EDA gene knockout human embryonic stem (hES) cell line by CRISPR-Cas9 technology. This cell line provides good materials for further studies of the roles ectodysplasin A plays in ectoderm differentiation and tooth development