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作 者:LI Ting-ting LU Na SHAO Yu-xin ZHANG Li-yang LU Lin LIU Zong-ping LUO Xu-gang LIAO Xiu-dong
机构地区:[1]Poultry Mineral Nutrition Laboratory,College of Animal Science and Technology,Yangzhou University,Yangzhou 225009,P.R.China [2]Mineral Nutrition Research Division,Institute of Animal Sciences,Chinese Academy of Agricultural Sciences,Beijing 100193,P.R.China [3]College of Veterinary Medicine,Yangzhou University,Yangzhou 225009,P.R.China
出 处:《Journal of Integrative Agriculture》2022年第7期2076-2085,共10页农业科学学报(英文版)
基 金:supported by the Key Program of the National Natural Science Foundation of China(31630073);the National Natural Science Foundation of China(31472116);the National Key R&D Program of China(2017YFD0502200);the China Agriculture Research System of MOF and MARA(CARS-41);the Agricultural Science and Technology Innovation Program(ASTIP-IAS09)。
摘 要:The aim of the study was to investigate whether phosphorus(P) transporters, type IIb sodium-dependent phosphate cotransporter(NaP-IIb) and inorganic phosphate transporter 2(PiT2), were directly involved in P absorption across primary cultured duodenal epithelial cell monolayers of chick embryos. The siRNAs against NaP-IIb or PiT2 were designed, synthesized and transfected into primary cultured duodenal epithelial cells of chick embryos. Then, the inhibitory efficiency of siRNAs against NaP-IIb or PiT2 was analyzed, and the most efficacious siRNAs were selected to be used for subsequent P absorption experiments. Briefly, primary cultured duodenal epithelial cells of chick embryos were transfected with either NaP-IIb or PiT2 siRNAs and grown in confluent monolayers on transwell plates. The untransfected or transfected cell monolayers were then incubated in an uptake medium containing 0 or 0.25 mmol L^(–1) of P as KH_(2) PO_(4) to measure the P absorption across duodenal epithelial cell monolayers. The results showed that among the siRNAs designed, si-1372 and si-890 were demonstrated to be the most effective in inhibiting the NaPIIb and PiT2 expressions, respectively. Supplemental P increased(P=0.065) the protein abundance of PiT2 and enhanced(P<0.0001) P absorption in primary cultured duodenal epithelial cell of chick embryos. Furthermore, NaPIIb silencing decreased(P=0.07) P absorption across duodenal epithelial cell monolayers, while PiT2 silencing had no effect(P=0.345). It is concluded that the NaP-IIb, but not PiT2, might be directly involved in the P absorption of chick duodenal epithelial cells.
关 键 词:BROILER phosphorus transporter phosphorus absorption primary cultured duodenal epithelial cell
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