To elucidate the structure characteristic, regulation of expression and the potential function of JWA——anovel rctinoic acid responsible and cytoskeleton associate gene, a rat JWA homologue gene and a 621-bp JWA prom...To elucidate the structure characteristic, regulation of expression and the potential function of JWA——anovel rctinoic acid responsible and cytoskeleton associate gene, a rat JWA homologue gene and a 621-bp JWA promoter fragment were cloned and analyzed. Using reverse transcription-polymerase chain reaction (RT-PCR), JWA mRNA expression in NIH3T3, K562 and human primary acute promyelocytic leukaemia (APL) cells have been investigated after treatment with all trans retinoic acid (ATRA), N-4-hydroxyphenyl-retinamide (4HPR), arsenic trioxide (As2O3), Phorbol-12-myristate-13-acetate (TPA) and dimethyl sulfoxide (DMSO). The results showed that there is a complete TPA responsive element (TRE) existed in the promoter of JWA at -437 to -443 bp; rat JWA homologue gene showed that there are four nucleotides different from human JWA within coding region. After treatment with TPA, an uneven pattern of JWA transcription existed in different cell lines, suggesting that even TPA induces cell differentiation in展开更多
Regulatory T （Treg） cells are necessary for immune system homeostasis and the prevention of autoimmune diseases. Foxp3 is specifically expressed in Treg cells and plays a key role in their differentiation and functi...Regulatory T （Treg） cells are necessary for immune system homeostasis and the prevention of autoimmune diseases. Foxp3 is specifically expressed in Treg cells and plays a key role in their differentiation and function. Foxp3＋ Treg cells are consisted of naturally occurring, thymus-derived Treg （nTreg） and peripheral-induced Treg （iTreg） cells that may have different functional characteristics or synergistic roles. AII-trans retinoic acid （atRA）, a vitamin A metabolite, regulates a wide range of biological processes, including cell differentiation and proliferation. Recent studies demonstrated that atRA also regulates the differentiation of T helper （Th） cells and Treg cells. Moreover, atRA also sustains nTreg stability under inflammatory conditions. In this review, we summarize the significant progress of our understanding of the role（s） and mechanisms of atRA in Treg biology.展开更多
Objective To study the protective effects of naja naja atra venom （NNAV） in a rat model of diabetic nephropathy （DN）. Methods The rat diabetes model was induced by intraperitoneal injection of streptozotocin （STZ...Objective To study the protective effects of naja naja atra venom （NNAV） in a rat model of diabetic nephropathy （DN）. Methods The rat diabetes model was induced by intraperitoneal injection of streptozotocin （STZ）. Thirty-two model rats were randomly divided into one DN group （n=8） and three treatment groups （n=8 each） that received NNAV at doses of 30, 90, or 270 I^g/（ks.day） via oral gavage, another eight rats as normal controls. After 12 weeks, all rats were sacrificed and the changes in serum and urine biological index levels were determined by colorimetric assay. Microalbumin （mALB）, N-acetyl-13- glucosaminidase （NAG） and cystatin C （CysC） concentrations were measured by ELISA. Renal tissues were sliced for pathological and immunohistochemical observations. Results Comparied with the DN group, serum glucose was decreased by 31.04%, total cholesterol 21.96%, triglyceride 23.78%, serum creatinine 19.83%, blood urea nitrogen 31.28%, urinary protein excretion 45.42%, mALB 10.42%, NAG 20.65%, CysC 19.57%, whereas albumin increased by 5.55%, high-density lipoprotein-cholesterol 59.09%, creatinine clearance 19.05% in the treatment group by NNAV administration at dose of 90 μg/（kg-day）. NNAV also reduced the levels of malondialdehyde in serum （22.56%） and kidney tissue （9.79%）, and increased superoxide dismutase concentration in serum （15%） and decreased it in renal tissue （8.85%）. In addition, under light microscopy kidney structure was improved and glomerular hypertrophy decreased by 8.29%. As shown by immunohistochemistry, NNAV inhibited transforming growth factorl by 6.70% and nuclear actor-KB by 5.15%.展开更多
基金This work was supported in part by the National Natural Science Foundation of China (Grant No. 30070664) the Natural Science Foundation of Jiangsu Province (Grant No. BK99133) the Creative Foundation of Nanjing Medical University (Grant No. Cx9902).
文摘To elucidate the structure characteristic, regulation of expression and the potential function of JWA——anovel rctinoic acid responsible and cytoskeleton associate gene, a rat JWA homologue gene and a 621-bp JWA promoter fragment were cloned and analyzed. Using reverse transcription-polymerase chain reaction (RT-PCR), JWA mRNA expression in NIH3T3, K562 and human primary acute promyelocytic leukaemia (APL) cells have been investigated after treatment with all trans retinoic acid (ATRA), N-4-hydroxyphenyl-retinamide (4HPR), arsenic trioxide (As2O3), Phorbol-12-myristate-13-acetate (TPA) and dimethyl sulfoxide (DMSO). The results showed that there is a complete TPA responsive element (TRE) existed in the promoter of JWA at -437 to -443 bp; rat JWA homologue gene showed that there are four nucleotides different from human JWA within coding region. After treatment with TPA, an uneven pattern of JWA transcription existed in different cell lines, suggesting that even TPA induces cell differentiation in
文摘Regulatory T （Treg） cells are necessary for immune system homeostasis and the prevention of autoimmune diseases. Foxp3 is specifically expressed in Treg cells and plays a key role in their differentiation and function. Foxp3＋ Treg cells are consisted of naturally occurring, thymus-derived Treg （nTreg） and peripheral-induced Treg （iTreg） cells that may have different functional characteristics or synergistic roles. AII-trans retinoic acid （atRA）, a vitamin A metabolite, regulates a wide range of biological processes, including cell differentiation and proliferation. Recent studies demonstrated that atRA also regulates the differentiation of T helper （Th） cells and Treg cells. Moreover, atRA also sustains nTreg stability under inflammatory conditions. In this review, we summarize the significant progress of our understanding of the role（s） and mechanisms of atRA in Treg biology.
基金supported by the Research Project of the Jiangsu Province Key Provincial Talents Program,RC2011112
文摘Objective To study the protective effects of naja naja atra venom （NNAV） in a rat model of diabetic nephropathy （DN）. Methods The rat diabetes model was induced by intraperitoneal injection of streptozotocin （STZ）. Thirty-two model rats were randomly divided into one DN group （n=8） and three treatment groups （n=8 each） that received NNAV at doses of 30, 90, or 270 I^g/（ks.day） via oral gavage, another eight rats as normal controls. After 12 weeks, all rats were sacrificed and the changes in serum and urine biological index levels were determined by colorimetric assay. Microalbumin （mALB）, N-acetyl-13- glucosaminidase （NAG） and cystatin C （CysC） concentrations were measured by ELISA. Renal tissues were sliced for pathological and immunohistochemical observations. Results Comparied with the DN group, serum glucose was decreased by 31.04%, total cholesterol 21.96%, triglyceride 23.78%, serum creatinine 19.83%, blood urea nitrogen 31.28%, urinary protein excretion 45.42%, mALB 10.42%, NAG 20.65%, CysC 19.57%, whereas albumin increased by 5.55%, high-density lipoprotein-cholesterol 59.09%, creatinine clearance 19.05% in the treatment group by NNAV administration at dose of 90 μg/（kg-day）. NNAV also reduced the levels of malondialdehyde in serum （22.56%） and kidney tissue （9.79%）, and increased superoxide dismutase concentration in serum （15%） and decreased it in renal tissue （8.85%）. In addition, under light microscopy kidney structure was improved and glomerular hypertrophy decreased by 8.29%. As shown by immunohistochemistry, NNAV inhibited transforming growth factorl by 6.70% and nuclear actor-KB by 5.15%.
