The scavenger receptor class B type I (SR-BI) is a high-density lipoprotein (HDL) receptor involved in reverse cholesterol transport. Some studies reported the association to be stronger in the presence of diabetes. T...The scavenger receptor class B type I (SR-BI) is a high-density lipoprotein (HDL) receptor involved in reverse cholesterol transport. Some studies reported the association to be stronger in the presence of diabetes. The full length gene encoding SR-BI is comprised in 13 exons that are alternatively spliced to produce two major transcripts: the full length SR-BI and the splice variant SR-BII, in which exon 12 is skipped. Considering that type 2 diabetes status is characterized by changes in the concentration of plasma lipids, modifications in lipoprotein size and composition, which may be important modulators of the SR-BI expression;the aims of the study were to examine the influence of SR-BI polymorphism (rs838895) on lipid profile and SR-BI mRNA expression in a population of diabetic patients living in Juana Koslay City. Blood samples were drawn from controls (n = 40) and Type 2 diabetic patients (n = 66) and DNA and total RNA were obtained. SR-BI mRNA expression was measured by RT-PCR and SR-BI polymorphism was detected by Tetra Primer ARMSPCR. Compared to controls, diabetic patients had higher fasting serum glucose, glycated hemoglobin, triglycerides, total cholesterol, lowdensity lipoprotein cholesterol, and lower highdensity lipoprotein cholesterol. SR-BI mRNA expression was lower in T2DM when compared to controls, suggesting that the hyperglycemia presents in T2DM patients down-regulates SR-BI mRNA expression. Interestingly, we found that decreased SR-BI expression resulted in markedly increased plasma LDL concentrations in T2DM subjects, and the overexpression of SRBII isoform is responsible for the markedly increased plasma LDL-c concentrations. The polymorphism (rs838895) did not modify the mRNA level of SR-BI in leucocytes from control and diabetic patients. This study provides novel evidence suggesting that hyperglycemia may affect reverse cholesterol transport by controlling SRBI expression in diabetic patients. LDL cholesterol levels are associated with low SR-BI mRNA expression in T2DM.展开更多
Class B scavenger receptors （SR-Bs） are cell surface glycoproteins involved in various physiological processes in vivo, including the transport and metabolism of lipids, binding and phagoeytosis of xenobiotics, and ...Class B scavenger receptors （SR-Bs） are cell surface glycoproteins involved in various physiological processes in vivo, including the transport and metabolism of lipids, binding and phagoeytosis of xenobiotics, and signaling. But little information is available about silkworm SR-Bs; it is necessary to study these SR-Bs for revealing their function. In this study, we cloned the full-length coding sequence of BrnSCRBQ4, a SR-B gene from the silkworm Bombyx mori L. We found that the BmSCRBQ4 gene consists of nine exons and eight introns, with an open reading frame of 1371 bp encoding 456 amino acids. Gene expression studies determined that BmSCRBQ4 messenger RNA （mRNA） was expressed in unfertilized eggs, during embryonic development and throughout the majority of the larval period. Expression of mRNA was detected in the mid gut, middle silk gland, posterior silk gland, head, integumentum, fat body, testes and the ovaries of the larval B. mori Dazao strain, as well as in the silkworm cell lines BmN and BmE. Protein expression studies found BmSCRBQ4 protein was expressed only in the testes, fat body and middle silk gland of larvae, as well as in the silkworm cell lines BmN and BmE. The BmSCRBQ4 protein showed variability in banding patterns in different tissues and cells when analyzed by Western blotting. Immunohistochemical staining showed that the BmSCRBQ4 protein localizes to the constitutive membranes or cellular membranes of these tissues. These results indicated that BmSCRBQ4 gene may play some physiologically relevant roles at the cell surface in each tissue.展开更多
Stroke is a devastating disease that occurs when a blood vessel in the brain is either blocked or ruptured,consequently leading to deficits in neurological function.Stroke consistently ranked as one of the top causes ...Stroke is a devastating disease that occurs when a blood vessel in the brain is either blocked or ruptured,consequently leading to deficits in neurological function.Stroke consistently ranked as one of the top causes of mortality,and with the mean age of incidence decreasing,there is renewed interest to seek novel therapeutic treatments.The Scavenger Receptor Class B type 1(SR-B1)is a multifunctional protein found on the surface of a variety of cells.Research has found that that SR-B1 primarily functions in an anti-inflammatory and antiatherosclerotic capacity.In this review,we discuss the characteristics of SR-B1 and focus on its potential correlation with the modifiable risk factors of stroke.SR-B1 likely has an impact on stroke through its interaction with smoking,diabetes mellitus,diet,physical inactivity,obesity,hypercholesterolemia,atherosclerosis,coronary heart disease,hypertension,and sickle cell disease,all of which are critical risk factors in the pathogenesis of stroke.展开更多
Objective To observe the effect of Shengqing Capsule(SC)on serum contents of TC,LDL-C,and HDLC,hepatic scavenger receptor BⅠ(SRBⅠ),and CD36 in rats with cholesterol calculus.Methods
OBJECTIVE:To investigate the hypoglycemic mechanism of modified Gegen Qinlian decoction(加味葛根芩连汤,MGQD)by examining its regulation of cholesterol transporter expression and DNA methylation,specifically the low-de...OBJECTIVE:To investigate the hypoglycemic mechanism of modified Gegen Qinlian decoction(加味葛根芩连汤,MGQD)by examining its regulation of cholesterol transporter expression and DNA methylation,specifically the low-density lipoprotein receptor(LDLR)and scavenger receptor class B type 1(SR-B1),in epididymal white adipose tissue(e WAT)and inguinal white adipose tissue(i WAT)of rats with type 2 diabetes mellitus(T2DM).METHODS:The control group(CON)consisted of ten Sprague-Dawley(SD)rats fed a standard chow diet,while 80 SD rats were fed a high-fat diet and administered streptozotocin intraperitoneally to induce diabetes.The diabetic rats were randomly assigned to four groups:T2DM,metformin(MET,200 mg/kg),low-dose MGQD(MGQDL,5 g/kg),and high-dose MGQD(MGQDH,10 g/kg),and received treatment via gavage for 14 weeks.Western blot(WB),quantitative real-time polymerase chain reaction(q PCR),and bisulfite sequencing PCR(BSP)were used to analyze protein levels,m RNA expression,and DNA methylation of Ldlr(gene encoding LDLR)and Srb1(gene encoding SR-B1).RESULTS:MGQD and metformin treatment significantly reduced blood glucose levels,restored LDLR and SR-B1 protein levels in e WAT,and effectively regulated the m RNA expression and non-cytosine-p-guanine(nonCp G)methylation of Srb1 in e WAT.A significant negative correlation was observed between the methylation of Srb1 in e WAT and its m RNA expression.However,MGQD and metformin had no significant effect on the protein levels,m RNA expression,or DNA methylation of Ldlr and Srb1 in i WAT.CONCLUSIONS:MGQD did not significantly affect LDLR and SR-B1 expression or gene methylation in i WAT.However,its hypoglycemic effect may be linked to cholesterol regulation in e WAT.Potential mechanisms include increased LDLR protein levels,which may enhance cholesterol uptake,and increased Srb1 methylation,which may suppress its expression and consequently reduce cholesterol efflux.展开更多
The worldwide declines in amphibian populations have largely been caused by infectious fungi and bacteria. Given that vertebrate immunity against these extracellular pathogens is primarily functioned by the major hist...The worldwide declines in amphibian populations have largely been caused by infectious fungi and bacteria. Given that vertebrate immunity against these extracellular pathogens is primarily functioned by the major histocompatibility complex（MHC） class Ⅱ molecules, the characterization and the evolution of amphibian MHC class Ⅱ genes have attracted increasing attention. The polymorphism of MHC class Ⅱ genes was found to be correlated with susceptibility to fungal pathogens in many amphibian species, suggesting the importance of studies on MHC class Ⅱ genes for amphibians. However, such studies on MHC class Ⅱ gene evolution have rarely been conducted on amphibians in China. In this study, we chose Omei treefrog（Rhacophorus omeimontis）, which lived moist environments easy for breeding bacteria, to study the polymorphism of its MHC class Ⅱ genes and the underlying evolutionary mechanisms. We amplified the entire MHC class ⅡB exon 2 sequence in the R. omeimontis using newly designed primers. We detected 102 putative alleles in 146 individuals. The number of alleles per individual ranged from one to seven, indicating that there are at least four loci containing MHC class ⅡB genes in R. omeimontis. The allelic polymorphism estimated from the 102 alleles in R. omeimontis was not high compared to that estimated in other anuran species. No significant gene recombination was detected in the 102 MHC class ⅡB exon 2 sequences. In contrast, both gene duplication and balancing selection greatly contributed to the variability in MHC class ⅡB exon 2 sequences of R. omeimontis. This study lays the groundwork for the future researches to comprehensively analyze the evolution of amphibian MHC genes and to assess the role of MHC gene polymorphisms in resistance against extracellular pathogens for amphibians in China.展开更多
为探讨血清淀粉样蛋白A(serum amyloid A,SAA)对巨噬细胞B类I型清道夫受体(scavenger receptor class B type I,SR-BI)的表达以及炎症反应的影响及分子机制,采用SAA、p38丝裂原活化蛋白激酶(p38 mitogen-activated protein kinase,p38-M...为探讨血清淀粉样蛋白A(serum amyloid A,SAA)对巨噬细胞B类I型清道夫受体(scavenger receptor class B type I,SR-BI)的表达以及炎症反应的影响及分子机制,采用SAA、p38丝裂原活化蛋白激酶(p38 mitogen-activated protein kinase,p38-MAPK)激动剂anisomycin或抑制剂SB203580处理THP-1巨噬细胞,以实时定量PCR、Western blot和ELISA分别检测细胞中SR-BI、炎症因子及磷酸化p38-MAPK的表达。结果显示,与对照组相比,SAA处理THP-1细胞后,SR-BI的表达下调,而炎症因子与磷酸化p38蛋白的表达则上调,且这种效应呈浓度和时间依赖性(P<0.05)。与SAA单独处理组比较,SAA与p38-MAPK激动剂anisomycin共孵育细胞后,细胞SR-BI表达下调,炎症因子及磷酸化p38蛋白表达增加(P<0.05);而SAA与p38-MAPK抑制剂SB203580共同处理细胞后,细胞SR-BI表达增加,炎症因子及磷酸化p38蛋白表达减少(P<0.05)。结果提示,SAA可促进THP-1巨噬细胞炎症反应,其机制与p38-MAPK的磷酸化及SR-BI表达的下调有关。展开更多
文摘The scavenger receptor class B type I (SR-BI) is a high-density lipoprotein (HDL) receptor involved in reverse cholesterol transport. Some studies reported the association to be stronger in the presence of diabetes. The full length gene encoding SR-BI is comprised in 13 exons that are alternatively spliced to produce two major transcripts: the full length SR-BI and the splice variant SR-BII, in which exon 12 is skipped. Considering that type 2 diabetes status is characterized by changes in the concentration of plasma lipids, modifications in lipoprotein size and composition, which may be important modulators of the SR-BI expression;the aims of the study were to examine the influence of SR-BI polymorphism (rs838895) on lipid profile and SR-BI mRNA expression in a population of diabetic patients living in Juana Koslay City. Blood samples were drawn from controls (n = 40) and Type 2 diabetic patients (n = 66) and DNA and total RNA were obtained. SR-BI mRNA expression was measured by RT-PCR and SR-BI polymorphism was detected by Tetra Primer ARMSPCR. Compared to controls, diabetic patients had higher fasting serum glucose, glycated hemoglobin, triglycerides, total cholesterol, lowdensity lipoprotein cholesterol, and lower highdensity lipoprotein cholesterol. SR-BI mRNA expression was lower in T2DM when compared to controls, suggesting that the hyperglycemia presents in T2DM patients down-regulates SR-BI mRNA expression. Interestingly, we found that decreased SR-BI expression resulted in markedly increased plasma LDL concentrations in T2DM subjects, and the overexpression of SRBII isoform is responsible for the markedly increased plasma LDL-c concentrations. The polymorphism (rs838895) did not modify the mRNA level of SR-BI in leucocytes from control and diabetic patients. This study provides novel evidence suggesting that hyperglycemia may affect reverse cholesterol transport by controlling SRBI expression in diabetic patients. LDL cholesterol levels are associated with low SR-BI mRNA expression in T2DM.
基金This research was supported by grants from the Na- tional Natural Science Foundation of China （Grant Nos. 31272505, 31172269 and 31360586）.
文摘Class B scavenger receptors （SR-Bs） are cell surface glycoproteins involved in various physiological processes in vivo, including the transport and metabolism of lipids, binding and phagoeytosis of xenobiotics, and signaling. But little information is available about silkworm SR-Bs; it is necessary to study these SR-Bs for revealing their function. In this study, we cloned the full-length coding sequence of BrnSCRBQ4, a SR-B gene from the silkworm Bombyx mori L. We found that the BmSCRBQ4 gene consists of nine exons and eight introns, with an open reading frame of 1371 bp encoding 456 amino acids. Gene expression studies determined that BmSCRBQ4 messenger RNA （mRNA） was expressed in unfertilized eggs, during embryonic development and throughout the majority of the larval period. Expression of mRNA was detected in the mid gut, middle silk gland, posterior silk gland, head, integumentum, fat body, testes and the ovaries of the larval B. mori Dazao strain, as well as in the silkworm cell lines BmN and BmE. Protein expression studies found BmSCRBQ4 protein was expressed only in the testes, fat body and middle silk gland of larvae, as well as in the silkworm cell lines BmN and BmE. The BmSCRBQ4 protein showed variability in banding patterns in different tissues and cells when analyzed by Western blotting. Immunohistochemical staining showed that the BmSCRBQ4 protein localizes to the constitutive membranes or cellular membranes of these tissues. These results indicated that BmSCRBQ4 gene may play some physiologically relevant roles at the cell surface in each tissue.
文摘Stroke is a devastating disease that occurs when a blood vessel in the brain is either blocked or ruptured,consequently leading to deficits in neurological function.Stroke consistently ranked as one of the top causes of mortality,and with the mean age of incidence decreasing,there is renewed interest to seek novel therapeutic treatments.The Scavenger Receptor Class B type 1(SR-B1)is a multifunctional protein found on the surface of a variety of cells.Research has found that that SR-B1 primarily functions in an anti-inflammatory and antiatherosclerotic capacity.In this review,we discuss the characteristics of SR-B1 and focus on its potential correlation with the modifiable risk factors of stroke.SR-B1 likely has an impact on stroke through its interaction with smoking,diabetes mellitus,diet,physical inactivity,obesity,hypercholesterolemia,atherosclerosis,coronary heart disease,hypertension,and sickle cell disease,all of which are critical risk factors in the pathogenesis of stroke.
文摘Objective To observe the effect of Shengqing Capsule(SC)on serum contents of TC,LDL-C,and HDLC,hepatic scavenger receptor BⅠ(SRBⅠ),and CD36 in rats with cholesterol calculus.Methods
基金National Natural Science Foundation of China:Investigation on the Mechanism of Gegen Qinlian Decoction in Lowering Blood Glucose Based on Improving Cholesterol Homeostasis of Lipid Rafts in Adipocytes(No.82060741)Study on the Cause of“Dampness Stagnating in Pi”in Type 2 Diabetes Mellitus by Overeating High Fat and Sugar Diet Based on Glycerol Transport Which Is Affected by Methylation/Hormones Signal(No.82160830)+4 种基金Investigation on the Mechanism of Gegen Qinlian Decoction in Lowering Blood Glucose Based on Improving Phosphatidylcholine Biosynthesis in Adipose Tissue(No.82360799)Jiangxi Provincial Administration of Traditional Chinese Medicine Science and Technology Program:the Relationship between Adipose Tissue and Spleen Image Based on Multivariate Analysis of Modern Literature(No.2020B0328)Ganpo Juncai-Training Program for Academic and Technical Leaders in Major Disciplines of the Province(Leading Talents-Academic Category)(20232BCJ22022)Jiangxi University of Chinese Medicine,First-level Discipline of Integrative Medicine(Jiangxi Province Double First-class Discipline)(zxyylxk20220103)Jiangxi University of Chinese Medicine Science and Technology Innovation Team Development Program(CXTD22007)。
文摘OBJECTIVE:To investigate the hypoglycemic mechanism of modified Gegen Qinlian decoction(加味葛根芩连汤,MGQD)by examining its regulation of cholesterol transporter expression and DNA methylation,specifically the low-density lipoprotein receptor(LDLR)and scavenger receptor class B type 1(SR-B1),in epididymal white adipose tissue(e WAT)and inguinal white adipose tissue(i WAT)of rats with type 2 diabetes mellitus(T2DM).METHODS:The control group(CON)consisted of ten Sprague-Dawley(SD)rats fed a standard chow diet,while 80 SD rats were fed a high-fat diet and administered streptozotocin intraperitoneally to induce diabetes.The diabetic rats were randomly assigned to four groups:T2DM,metformin(MET,200 mg/kg),low-dose MGQD(MGQDL,5 g/kg),and high-dose MGQD(MGQDH,10 g/kg),and received treatment via gavage for 14 weeks.Western blot(WB),quantitative real-time polymerase chain reaction(q PCR),and bisulfite sequencing PCR(BSP)were used to analyze protein levels,m RNA expression,and DNA methylation of Ldlr(gene encoding LDLR)and Srb1(gene encoding SR-B1).RESULTS:MGQD and metformin treatment significantly reduced blood glucose levels,restored LDLR and SR-B1 protein levels in e WAT,and effectively regulated the m RNA expression and non-cytosine-p-guanine(nonCp G)methylation of Srb1 in e WAT.A significant negative correlation was observed between the methylation of Srb1 in e WAT and its m RNA expression.However,MGQD and metformin had no significant effect on the protein levels,m RNA expression,or DNA methylation of Ldlr and Srb1 in i WAT.CONCLUSIONS:MGQD did not significantly affect LDLR and SR-B1 expression or gene methylation in i WAT.However,its hypoglycemic effect may be linked to cholesterol regulation in e WAT.Potential mechanisms include increased LDLR protein levels,which may enhance cholesterol uptake,and increased Srb1 methylation,which may suppress its expression and consequently reduce cholesterol efflux.
基金supported by the National Natural Science Foundation of China(No.31201713,No.31270425 and No.31470442)
文摘The worldwide declines in amphibian populations have largely been caused by infectious fungi and bacteria. Given that vertebrate immunity against these extracellular pathogens is primarily functioned by the major histocompatibility complex（MHC） class Ⅱ molecules, the characterization and the evolution of amphibian MHC class Ⅱ genes have attracted increasing attention. The polymorphism of MHC class Ⅱ genes was found to be correlated with susceptibility to fungal pathogens in many amphibian species, suggesting the importance of studies on MHC class Ⅱ genes for amphibians. However, such studies on MHC class Ⅱ gene evolution have rarely been conducted on amphibians in China. In this study, we chose Omei treefrog（Rhacophorus omeimontis）, which lived moist environments easy for breeding bacteria, to study the polymorphism of its MHC class Ⅱ genes and the underlying evolutionary mechanisms. We amplified the entire MHC class ⅡB exon 2 sequence in the R. omeimontis using newly designed primers. We detected 102 putative alleles in 146 individuals. The number of alleles per individual ranged from one to seven, indicating that there are at least four loci containing MHC class ⅡB genes in R. omeimontis. The allelic polymorphism estimated from the 102 alleles in R. omeimontis was not high compared to that estimated in other anuran species. No significant gene recombination was detected in the 102 MHC class ⅡB exon 2 sequences. In contrast, both gene duplication and balancing selection greatly contributed to the variability in MHC class ⅡB exon 2 sequences of R. omeimontis. This study lays the groundwork for the future researches to comprehensively analyze the evolution of amphibian MHC genes and to assess the role of MHC gene polymorphisms in resistance against extracellular pathogens for amphibians in China.
基金supported by grants from the National Natural Science Foundation of China(No.81100211)the Natural Science Foundation of Hunan Province+7 种基金China(No.14JJ208414JJ5016)the Science and Technology Project of Hengyang CityHunan ProvinceChina(No.2013KJ04)the Construct Program of the Key Discipline in Hunan ProvinceChina(Basic Medicine Sciences in University of South China)Zhengxiang Scholar Program of the University of South China
文摘为探讨血清淀粉样蛋白A(serum amyloid A,SAA)对巨噬细胞B类I型清道夫受体(scavenger receptor class B type I,SR-BI)的表达以及炎症反应的影响及分子机制,采用SAA、p38丝裂原活化蛋白激酶(p38 mitogen-activated protein kinase,p38-MAPK)激动剂anisomycin或抑制剂SB203580处理THP-1巨噬细胞,以实时定量PCR、Western blot和ELISA分别检测细胞中SR-BI、炎症因子及磷酸化p38-MAPK的表达。结果显示,与对照组相比,SAA处理THP-1细胞后,SR-BI的表达下调,而炎症因子与磷酸化p38蛋白的表达则上调,且这种效应呈浓度和时间依赖性(P<0.05)。与SAA单独处理组比较,SAA与p38-MAPK激动剂anisomycin共孵育细胞后,细胞SR-BI表达下调,炎症因子及磷酸化p38蛋白表达增加(P<0.05);而SAA与p38-MAPK抑制剂SB203580共同处理细胞后,细胞SR-BI表达增加,炎症因子及磷酸化p38蛋白表达减少(P<0.05)。结果提示,SAA可促进THP-1巨噬细胞炎症反应,其机制与p38-MAPK的磷酸化及SR-BI表达的下调有关。
