AIM:To investigate the sphingosine 1phosphate (S1P) receptor expression profile in human esophageal cancer cells and the effects of S1P5 on proliferation and migration of human esophageal cancer cells. METHODS: S1P re...AIM:To investigate the sphingosine 1phosphate (S1P) receptor expression profile in human esophageal cancer cells and the effects of S1P5 on proliferation and migration of human esophageal cancer cells. METHODS: S1P receptor expression profile in human esophageal squamous cell carcinoma cell line Eca109 was detected by semiquantitative reverse trans cription polymerase chain reaction. Eca109 cells were stably transfected with S1P5EGFP or controlEGFP constructs. The relation between the responses of cell proliferationand migration to S1P and S1P5 expres sion was evaluated by 3(4,5dimethylthiazol2yl)2,5diphenyl tetrazolium bromide and migration assay, respectively. RESULTS: Both normal human esophageal mucosal epithelium and Eca109 cells expressed S1P1, S1P2, S1P3 and S1P5, respectively. Esophageal mucosal epithelium expressed S1P5 at a higher level than Eca109 cell line. S1P5 overexpressing Eca109 cells displayed spindle cell morphology with elongated and extended filopodialike projections. The proliferation response of S1P5transfected Eca109 cells was lower than that of control vectortransfected cells with or without S1P stimulation (P < 0.05 or 0.01). S1P significantly inhibited the migration of S1P5transfected Eca109 cells (P < 0.001). However, without S1P in transwell lower chamber, the number of migrated S1P5transfected Eca109 cells was greater than that of control vectortransfected Eca109 cells (P < 0.001).CONCLUSION: S1P binding to S1P5 inhibits the proliferation and migration of S1P5transfected Eca109 cells. Esophageal cancer cells may downregulate the expression of S1P5 to escape the inhibitory effect.展开更多
Inflammatory bowel disease(IBD)is chronic inflammation of the gastrointestinal tract that has a high epidemiological prevalence worldwide.The increasing disease burden worldwide,lack of response to current biologic th...Inflammatory bowel disease(IBD)is chronic inflammation of the gastrointestinal tract that has a high epidemiological prevalence worldwide.The increasing disease burden worldwide,lack of response to current biologic therapeutics,and treatment-related immunogenicity have led to major concerns regarding the clinical management of IBD patients and treatment efficacy.Understanding disease pathogenesis and disease-related molecular mechanisms is the most important goal in developing new and effective therapeutics.Sphingosine-1-phosphate(S1P)receptor(S1PR)modulators form a class of oral small molecule drugs currently in clinical development for IBD have shown promising effects on disease improvement.S1P is a sphingosine-derived phospholipid that acts by binding to its receptor S1PR and is involved in the regulation of several biological processes including cell survival,differentiation,migration,proliferation,immune response,and lymphocyte trafficking.T lymphocytes play an important role in regulating inflammatory responses.In inflamed IBD tissue,an imbalance between T helper(Th)and regulatory T lymphocytes and Th cytokine levels was found.The S1P/S1PR signaling axis and metabolism have been linked to inflammatory responses in IBD.S1P modulators targeting S1PRs and S1P metabolism have been developed and shown to regulate inflammatory responses by affecting lymphocyte trafficking,lymphocyte number,lymphocyte activity,cytokine production,and contributing to gut barrier function.展开更多
Carbamoyl phosphate synthetase i （CPS1） deficiency （CPS1D） is an inborn error of the urea cycle having autosomal （2q34） recessive inheritance that can cause hyperammonemia and neonatal death or mental retardatio...Carbamoyl phosphate synthetase i （CPS1） deficiency （CPS1D） is an inborn error of the urea cycle having autosomal （2q34） recessive inheritance that can cause hyperammonemia and neonatal death or mental retardation. We analyzed the effects on CPS1 activity, kinetic parameters and enzyme stability of missense mutations reported in patients with CPS1 deficiency that map in the 20-kDa C-terminal domain of the enzyme. This domain turns on or off the enzyme depending on whether the essential allosteric activator of CPS 1, N-acetyl- L-glutamate （NAG）, is bound or is not bound to it. To carry out the present studies, we exploited a novel system that allows the expression in vitro and the purification of human CPS1, thus permitting site-directed mutagenesis. These studies have clarified disease causation by individual mutations, identifying functionally important residues, and revealing that a number of mutations decrease the affinity of the enzyme for NAG. Patients with NAG affinity-decreasing mutations might benefit from NAG site saturation therapy with N-carbamyl-L- glutamate （a registered drug, the analog of NAG）. Our results, together with additional present and prior site-directed mutagenesis data for other residues mapping in this domain, suggest an NAG-triggered conformational change in the 134-~4 loop of the C-terminal domain of this enzyme. This change might be an early event in the NAG activation process. Molecular dynamics simulations that were restrained according to the observed effects of the mutations are consistent with this hypothesis, providing further backing for this structurally plausible signaling mechanism by which NAG could trigger urea cycle activation via CPS1.展开更多
Background:The lysosphingolipid,sphingosine-1-phosphate,is a well-described and potent pro-angiogenic factor.Receptors,as well as the sphingosine phosphorylating enzyme sphingosine kinase 1,are expressed in the placen...Background:The lysosphingolipid,sphingosine-1-phosphate,is a well-described and potent pro-angiogenic factor.Receptors,as well as the sphingosine phosphorylating enzyme sphingosine kinase 1,are expressed in the placentomes of sheep and the decidua of rodents;however,a function for this signaling pathway during pregnancy has not been established.The objective of this study was to investigate whether sphingosine-1-phosphate promoted angiogenesis within the placentomes of pregnant ewes.Ewes were given daily jugular injections of FTY720(2-amino-2[2-(−4-octylphenyl)ethyl]propate-1,3-diol hydrochloride),an S1P analog.Results:FTY720 infusion from days 30 to 60 of pregnancy did not alter maternal organ weights nor total number or mass of placentomes,but did alter placentome histoarchitecture.Interdigitation of caruncular crypts and cotyledonary villi was decreased,as was the relative area of cotyledonary tissue within placentomes.Also,the percentage of area occupied by cotyledonary villi per unit of placentome was increased,while the thickness of the caruncular capsule was decreased in ewes treated with FTY720.Further,FTY720 infusion decreased the number and density of blood vessels within caruncular tissue near the placentome capsule where the crypts emerge from the capsule.Finally,FTY720 infusion decreased asparagine and glutamine in amniotic fluid and methionine in allantoic fluid,and decreased the crown rump length of day 60 fetuses.Conclusions:While members of the sphingosine-1-phosphate signaling pathway have been characterized within the uteri and placentae of sheep and mice,the present study uses FTY720 to address the influence of S1P signaling on placental development.We present evidence that modulation of the S1P signaling pathway results in the alteration of caruncular vasculature,placentome architecture,abundance of amino acids in allantoic and amniotic fluids,and fetal growth during pregnancy in sheep.The marked morphological changes in placentome histoarchitecture,including alteration in the vasculature,may be relevant to fetal growth and survival.It is somewhat surprising that fetal length was reduced as early as day 60,because fetal growth in sheep is greatest after day 60.The subtle changes observed in the fetuses of ewes exposed to FTY720 may indicate an adaptive response of the fetuses to cope with altered placental morphology.展开更多
Controlled release of the functional factors is the key to improve clinical therapeutic efficacy during the tissue repair and regeneration. The thrce-dimensional （3D） scaffold can provide not only physical propertie...Controlled release of the functional factors is the key to improve clinical therapeutic efficacy during the tissue repair and regeneration. The thrce-dimensional （3D） scaffold can provide not only physical properties such as high strength and porosity hut also an optimal environment to enhance tissue regeneration. Sphingosine 1-phosphate （SIP）, an angiogenlc factor, was loaded into mesoporous silica nanoparticles （MSNs） and then incorporated into poly （ L-lactic add ） （ PLLA ） nanofibrons scaffold, which was fabricated by thermally induced phase separation （TIPS） method. The prepared scaffolds were examined by attenuated total reflection Fourier transform infrared spectroscopy （ATR-FTIR）, scanning electron microscopy （ SEM）, and transmission electron microscopy （TEM） and compressive mechanical test. The ATR-FTIR result demonstrated the existence of MSNs in the PLLA nanofibrous scaffold. The SEM images showed that PLLA scaffold had regular pore channel, interconnected pores and nanofibrous structure. The addition of MSNs at appropriate content had no visible effect on the structure of scaffold. The compressive modulus of scaffold containing MSNs was higher than that of the scaffold without MSNs. Furthermore, fluorescein isothiocyanate （FTTC） was used as model molecule to investigate the release behavior of SIP from MSNs- incorporated PLLA （MSNs/PLLA） nanofibrons scaffold. The result showed that the composite scaffold largely reduced the initial burst release and exhibited prolonged release of FITC than MSNs. Thus, these results indicated that SIP-loaded composite uanofibrons scaffold has potential applications for bone tissue engneering.展开更多
The liver is the central organ involved in lipid metabolism. Dyslipidemia and its related disorders, including non-alcoholic fatty liver disease(NAFLD), obesity and other metabolic diseases, are of increasing public h...The liver is the central organ involved in lipid metabolism. Dyslipidemia and its related disorders, including non-alcoholic fatty liver disease(NAFLD), obesity and other metabolic diseases, are of increasing public health concern due to their increasing prevalence in the population. Besides their well-characterized functions in cholesterol homoeostasis and nutrient absorption, bile acids are also important metabolic regulators and function as signaling hormones by activating specific nuclear receptors, G-protein coupled receptors, and multiple signaling pathways. Recent studies identified a new signaling pathway by which conjugated bile acids(CBA) activate the extracellular regulated protein kinases(ERK1/2) and protein kinase B(AKT) signaling pathway via sphingosine-1-phosphate receptor 2(S1PR2). CBA-induced activation of S1PR2 is a key regulator of sphingosine kinase 2(Sph K2) andhepatic gene expression. This review focuses on recent findings related to the role of bile acids/S1PR2-mediated signaling pathways in regulating hepatic lipid metabolism.展开更多
O-linked N-acetyl-glucosamine glycosylation(O-GlcNAcylation)of intracellular proteins is a dynamic process broadly implicated in age-related disease,yet it remains uncharacterized whether and how O-GlcNAcylation contr...O-linked N-acetyl-glucosamine glycosylation(O-GlcNAcylation)of intracellular proteins is a dynamic process broadly implicated in age-related disease,yet it remains uncharacterized whether and how O-GlcNAcylation contributes to the natural aging process.O-GlcNAc transferase(OGT)and the opposing enzyme O-GlcNAcase(OGA)control this nutrient-sensing protein modification in cells.Here,we show that global O-GlcNAc levels are increased in multiple tissues of aged mice.In aged liver,carbamoyl phosphate synthetase 1(CPS1)is among the most heavilyO-GlcNAcylated proteins.CPS1O-GlcNAcylation is reversed by calorie restriction and is sensitive to genetic and pharmacological manipulations of theO-GlcNAc pathway.High glucose stimulates CPS1O-GlcNAcylation and inhibits CPS1 activity.Liver-specific deletion of OGT potentiates CPS1 activity and renders CPS1 irresponsive to further stimulation by a prolonged fasting.Our results identify CPS1 O-GlcNAcylation as a key nutrient-sensing regulatory step in the urea cycle during aging and dietary restriction,implying a role for mitochondrial O-GlcNAcylation in nutritional regulation of longevity.展开更多
Background:Shuangshen granule s(SSGs) are extensively utilized for the treatment of lung cancer in China and have been reported to possess tumor-protective and anti-metastatic effects.Therefore,it is crucial to unders...Background:Shuangshen granule s(SSGs) are extensively utilized for the treatment of lung cancer in China and have been reported to possess tumor-protective and anti-metastatic effects.Therefore,it is crucial to understand the precise mechanism.Building upon the findings of our previous study,the objective of the present study was to explore the impact of S SGs on the sphingosine-1-phosphate receptor-1(S1PR1)/signal transducer and activator of transcription 3(STAT3) axis,as well as the recruitment of myeloid-derived suppressor cells(MDSCs) during the formation of the premetastatic niches(PMNs).Methods:In a mouse xenograft model utilizing Lewis lung carcinoma(LLC) cells that express green fluorescent protein(GFP),the initiation of lung metastasis was monitored every three days until day 35 following transplantation.Lung metastasis,MD SC recruitment,the expression of PMN and S1PR1/STAT3 axis biomarkers,as well as the blood levels of granulocyte-mac rophage colony-stimulating factor(GM-CSF) and transforming growth factor-β(TGF-β) were assessed in the SSG treatment and control groups.Results:The LLC cells did not reach the lung until 14-17 days following subcutaneous implantation,which was concurrent with the formation of lung PMNs.S SG significantly postponed the initiation of lung metastasis and reduced the recruitment of MDSCs to the lung PMNs.S SG also suppre ssed the S1PR1/STAT3 axis in tumor tissue s,bone marrow,and lung PMNs.Additionally,SSG suppres sed the blood levels of GM-CSF and TGF-β,as well as the PMN markers,matrix metalloproteinase-9 and versican.Conclusion:Our findings suggested that SSG suppressed the development of MD SC-mediated PMNs by inhibiting the S1PR1/STAT3 axis,consequently postponing the initiation of lung metastasis.展开更多
The biodegradable plastic poly(lactic acid)(PLA)has been widely used to reduce plastic pollution in the environment,but PLA does not readily degrade completely and is more prone to form microplastics(MPs)and age.In th...The biodegradable plastic poly(lactic acid)(PLA)has been widely used to reduce plastic pollution in the environment,but PLA does not readily degrade completely and is more prone to form microplastics(MPs)and age.In this study,MP-PLA was aged by simulating the behavior of the marine environment and combined with plastic additive tris(1-chloro-2-propyl)phosphate(TCPP)according to their susceptibility to adsorb environmental pollutants.Mussels were the exposed subjects,and exposure concentrations of MPs and TCPP were set at 0.2 mg/L,1 mg/L,and 0.5μg/L,respectively.The ecotoxicity of PLA,aged-PLA,TCPP,and TCPP+aged-PLA was compared based on the result that aged-PLA could adsorb more TCPP.Biomarker assays revealed that mussels ingesting and accumulating contaminants underwent a severe oxidative(ROS)and immune stress response in the organism,with disruption of energy metabolism for energy supply,leading to apoptosis,resulting in tissue damage,and disruption of the homeostasis of the symbiotic intestinal microbiota.Comparisons showed that aging enhanced the adverse effects of PLA and ecotoxicological effects are further exacerbated by the adsorption of TCPP on aged-PLA.Therefore,with the widespread use of degradable plastics,long-term environmental impacts such as incomplete degradation and release of additives must be a concern.展开更多
基金Supported by The Key Project of Ministry of Education, No. 209105Sichuan Youth Science and Technology Foundation, No. 08ZQ026-081Key Laboratory Foundation of North Sichuan Medical College, No. KFJJ (08)-03
文摘AIM:To investigate the sphingosine 1phosphate (S1P) receptor expression profile in human esophageal cancer cells and the effects of S1P5 on proliferation and migration of human esophageal cancer cells. METHODS: S1P receptor expression profile in human esophageal squamous cell carcinoma cell line Eca109 was detected by semiquantitative reverse trans cription polymerase chain reaction. Eca109 cells were stably transfected with S1P5EGFP or controlEGFP constructs. The relation between the responses of cell proliferationand migration to S1P and S1P5 expres sion was evaluated by 3(4,5dimethylthiazol2yl)2,5diphenyl tetrazolium bromide and migration assay, respectively. RESULTS: Both normal human esophageal mucosal epithelium and Eca109 cells expressed S1P1, S1P2, S1P3 and S1P5, respectively. Esophageal mucosal epithelium expressed S1P5 at a higher level than Eca109 cell line. S1P5 overexpressing Eca109 cells displayed spindle cell morphology with elongated and extended filopodialike projections. The proliferation response of S1P5transfected Eca109 cells was lower than that of control vectortransfected cells with or without S1P stimulation (P < 0.05 or 0.01). S1P significantly inhibited the migration of S1P5transfected Eca109 cells (P < 0.001). However, without S1P in transwell lower chamber, the number of migrated S1P5transfected Eca109 cells was greater than that of control vectortransfected Eca109 cells (P < 0.001).CONCLUSION: S1P binding to S1P5 inhibits the proliferation and migration of S1P5transfected Eca109 cells. Esophageal cancer cells may downregulate the expression of S1P5 to escape the inhibitory effect.
文摘Inflammatory bowel disease(IBD)is chronic inflammation of the gastrointestinal tract that has a high epidemiological prevalence worldwide.The increasing disease burden worldwide,lack of response to current biologic therapeutics,and treatment-related immunogenicity have led to major concerns regarding the clinical management of IBD patients and treatment efficacy.Understanding disease pathogenesis and disease-related molecular mechanisms is the most important goal in developing new and effective therapeutics.Sphingosine-1-phosphate(S1P)receptor(S1PR)modulators form a class of oral small molecule drugs currently in clinical development for IBD have shown promising effects on disease improvement.S1P is a sphingosine-derived phospholipid that acts by binding to its receptor S1PR and is involved in the regulation of several biological processes including cell survival,differentiation,migration,proliferation,immune response,and lymphocyte trafficking.T lymphocytes play an important role in regulating inflammatory responses.In inflamed IBD tissue,an imbalance between T helper(Th)and regulatory T lymphocytes and Th cytokine levels was found.The S1P/S1PR signaling axis and metabolism have been linked to inflammatory responses in IBD.S1P modulators targeting S1PRs and S1P metabolism have been developed and shown to regulate inflammatory responses by affecting lymphocyte trafficking,lymphocyte number,lymphocyte activity,cytokine production,and contributing to gut barrier function.
基金supported by grants from the Alicia Koplowitz Foundation, the Valencian government (No. Prometeo II/2014/ 029 to V.R.)the Spanish government (Nos. BFU2011-30407 to V.R., BFU2012-30770 to J.G. and a FPU fellowship to C.D.-F.)the Swiss National Science Foundation (No. 310030_127184 to J.H.)
文摘Carbamoyl phosphate synthetase i （CPS1） deficiency （CPS1D） is an inborn error of the urea cycle having autosomal （2q34） recessive inheritance that can cause hyperammonemia and neonatal death or mental retardation. We analyzed the effects on CPS1 activity, kinetic parameters and enzyme stability of missense mutations reported in patients with CPS1 deficiency that map in the 20-kDa C-terminal domain of the enzyme. This domain turns on or off the enzyme depending on whether the essential allosteric activator of CPS 1, N-acetyl- L-glutamate （NAG）, is bound or is not bound to it. To carry out the present studies, we exploited a novel system that allows the expression in vitro and the purification of human CPS1, thus permitting site-directed mutagenesis. These studies have clarified disease causation by individual mutations, identifying functionally important residues, and revealing that a number of mutations decrease the affinity of the enzyme for NAG. Patients with NAG affinity-decreasing mutations might benefit from NAG site saturation therapy with N-carbamyl-L- glutamate （a registered drug, the analog of NAG）. Our results, together with additional present and prior site-directed mutagenesis data for other residues mapping in this domain, suggest an NAG-triggered conformational change in the 134-~4 loop of the C-terminal domain of this enzyme. This change might be an early event in the NAG activation process. Molecular dynamics simulations that were restrained according to the observed effects of the mutations are consistent with this hypothesis, providing further backing for this structurally plausible signaling mechanism by which NAG could trigger urea cycle activation via CPS1.
基金National Research Initiative Competitive Grant No.2009-35203-05725(KJB and GAJ)Fellowship No.2008-35203-18830(KAD)from the USDA National Institute of Food and Agriculture.
文摘Background:The lysosphingolipid,sphingosine-1-phosphate,is a well-described and potent pro-angiogenic factor.Receptors,as well as the sphingosine phosphorylating enzyme sphingosine kinase 1,are expressed in the placentomes of sheep and the decidua of rodents;however,a function for this signaling pathway during pregnancy has not been established.The objective of this study was to investigate whether sphingosine-1-phosphate promoted angiogenesis within the placentomes of pregnant ewes.Ewes were given daily jugular injections of FTY720(2-amino-2[2-(−4-octylphenyl)ethyl]propate-1,3-diol hydrochloride),an S1P analog.Results:FTY720 infusion from days 30 to 60 of pregnancy did not alter maternal organ weights nor total number or mass of placentomes,but did alter placentome histoarchitecture.Interdigitation of caruncular crypts and cotyledonary villi was decreased,as was the relative area of cotyledonary tissue within placentomes.Also,the percentage of area occupied by cotyledonary villi per unit of placentome was increased,while the thickness of the caruncular capsule was decreased in ewes treated with FTY720.Further,FTY720 infusion decreased the number and density of blood vessels within caruncular tissue near the placentome capsule where the crypts emerge from the capsule.Finally,FTY720 infusion decreased asparagine and glutamine in amniotic fluid and methionine in allantoic fluid,and decreased the crown rump length of day 60 fetuses.Conclusions:While members of the sphingosine-1-phosphate signaling pathway have been characterized within the uteri and placentae of sheep and mice,the present study uses FTY720 to address the influence of S1P signaling on placental development.We present evidence that modulation of the S1P signaling pathway results in the alteration of caruncular vasculature,placentome architecture,abundance of amino acids in allantoic and amniotic fluids,and fetal growth during pregnancy in sheep.The marked morphological changes in placentome histoarchitecture,including alteration in the vasculature,may be relevant to fetal growth and survival.It is somewhat surprising that fetal length was reduced as early as day 60,because fetal growth in sheep is greatest after day 60.The subtle changes observed in the fetuses of ewes exposed to FTY720 may indicate an adaptive response of the fetuses to cope with altered placental morphology.
基金National Natural Science Foundations of China(Nos.31271028,31570984)International Cooperation Fund of the Science and Technology Commission of Shanghai Municipality,China(No.15540723400)+2 种基金Open Foundation of State Key Laboratory for Modification of Chemical Fibers,Polymer Materials,China(No.LK1416)the Innovation Funds of Donghua University,China(No.15D310516)“111 Project” Biomedical Textile Materials Science and Technology,China(No.B07024)
文摘Controlled release of the functional factors is the key to improve clinical therapeutic efficacy during the tissue repair and regeneration. The thrce-dimensional （3D） scaffold can provide not only physical properties such as high strength and porosity hut also an optimal environment to enhance tissue regeneration. Sphingosine 1-phosphate （SIP）, an angiogenlc factor, was loaded into mesoporous silica nanoparticles （MSNs） and then incorporated into poly （ L-lactic add ） （ PLLA ） nanofibrons scaffold, which was fabricated by thermally induced phase separation （TIPS） method. The prepared scaffolds were examined by attenuated total reflection Fourier transform infrared spectroscopy （ATR-FTIR）, scanning electron microscopy （ SEM）, and transmission electron microscopy （TEM） and compressive mechanical test. The ATR-FTIR result demonstrated the existence of MSNs in the PLLA nanofibrous scaffold. The SEM images showed that PLLA scaffold had regular pore channel, interconnected pores and nanofibrous structure. The addition of MSNs at appropriate content had no visible effect on the structure of scaffold. The compressive modulus of scaffold containing MSNs was higher than that of the scaffold without MSNs. Furthermore, fluorescein isothiocyanate （FTTC） was used as model molecule to investigate the release behavior of SIP from MSNs- incorporated PLLA （MSNs/PLLA） nanofibrons scaffold. The result showed that the composite scaffold largely reduced the initial burst release and exhibited prolonged release of FITC than MSNs. Thus, these results indicated that SIP-loaded composite uanofibrons scaffold has potential applications for bone tissue engneering.
基金supported by A.D.Williams Award (to Huiping Zhou)National Institutes of Health (NIH,No.R01 DK-057543 to Phillip B.Hylemon and Huiping Zhou)+1 种基金supported by VA Merit Awards (No.1BX0013828-01 to Phillip B.HylemonNo.1I01BX001390 to Huiping Zhou)
文摘The liver is the central organ involved in lipid metabolism. Dyslipidemia and its related disorders, including non-alcoholic fatty liver disease(NAFLD), obesity and other metabolic diseases, are of increasing public health concern due to their increasing prevalence in the population. Besides their well-characterized functions in cholesterol homoeostasis and nutrient absorption, bile acids are also important metabolic regulators and function as signaling hormones by activating specific nuclear receptors, G-protein coupled receptors, and multiple signaling pathways. Recent studies identified a new signaling pathway by which conjugated bile acids(CBA) activate the extracellular regulated protein kinases(ERK1/2) and protein kinase B(AKT) signaling pathway via sphingosine-1-phosphate receptor 2(S1PR2). CBA-induced activation of S1PR2 is a key regulator of sphingosine kinase 2(Sph K2) andhepatic gene expression. This review focuses on recent findings related to the role of bile acids/S1PR2-mediated signaling pathways in regulating hepatic lipid metabolism.
基金was supported by grants from National Institutes of Health(R01DK089098 and P01DK57751)American Diabetes Association(1-19-IBS-119)+1 种基金X.Y.and a Glenn/AFAR Scholarship for Research in the Biology of Aging to M.-D.LYale School of Medicine and by the Office of The Director,National Institutes of Health(S10OD02365101A1,S10OD019967,and S10OD018034).
文摘O-linked N-acetyl-glucosamine glycosylation(O-GlcNAcylation)of intracellular proteins is a dynamic process broadly implicated in age-related disease,yet it remains uncharacterized whether and how O-GlcNAcylation contributes to the natural aging process.O-GlcNAc transferase(OGT)and the opposing enzyme O-GlcNAcase(OGA)control this nutrient-sensing protein modification in cells.Here,we show that global O-GlcNAc levels are increased in multiple tissues of aged mice.In aged liver,carbamoyl phosphate synthetase 1(CPS1)is among the most heavilyO-GlcNAcylated proteins.CPS1O-GlcNAcylation is reversed by calorie restriction and is sensitive to genetic and pharmacological manipulations of theO-GlcNAc pathway.High glucose stimulates CPS1O-GlcNAcylation and inhibits CPS1 activity.Liver-specific deletion of OGT potentiates CPS1 activity and renders CPS1 irresponsive to further stimulation by a prolonged fasting.Our results identify CPS1 O-GlcNAcylation as a key nutrient-sensing regulatory step in the urea cycle during aging and dietary restriction,implying a role for mitochondrial O-GlcNAcylation in nutritional regulation of longevity.
基金supported by the Special Training of Scientific and Technological Talents,China Academy of Chinese Medical Sciences (grant number ZZ13-YQ-023,ZZ13-YQ-028)the National Natural Science Foundation of China(grant number 82174465,82074338,82274609,82104961,82174463)+7 种基金the Beijing Municipal Science and Technology Commission (grant number Z181100001618006)Scientificand Technological Innovation Project of China Academy of Chinese Medical Sciences (grant number CI2021A01810,CI2021A01814,CI2021A01808,CI2021B009)Traditional Chinese Medicine Innovation Team Project of the National Administration of Traditional Chinese Medicine(grant number ZYYCXTD-C-202205)Central High-Level Traditional Chinese Medicine Hospital Clinical Research and Achievement Transformation Capacity Enhancement Project-Special Project Inheriting the Academic Experienceof Renowned Traditional Chinese Medicine Experts(HLCMHPP2023012)China Academy of Chinese Medical Sciences Special Project for Research and Development of Superior Diseases,Hospital Preparations,New Drugs(ZZ15-XY-PT-01)Xu Hang Project for Cultivating Young Top Talents at Guang'anmen Hospital (CZ40908)The Fundamental Research Funds for the Central Public Welfare Research Institutes (ZZ17XRZ-023)Clinical Research Expenses of the Central High-level Hospital of Traditional Chinese Medicine (HLCMHPP2023101)
文摘Background:Shuangshen granule s(SSGs) are extensively utilized for the treatment of lung cancer in China and have been reported to possess tumor-protective and anti-metastatic effects.Therefore,it is crucial to understand the precise mechanism.Building upon the findings of our previous study,the objective of the present study was to explore the impact of S SGs on the sphingosine-1-phosphate receptor-1(S1PR1)/signal transducer and activator of transcription 3(STAT3) axis,as well as the recruitment of myeloid-derived suppressor cells(MDSCs) during the formation of the premetastatic niches(PMNs).Methods:In a mouse xenograft model utilizing Lewis lung carcinoma(LLC) cells that express green fluorescent protein(GFP),the initiation of lung metastasis was monitored every three days until day 35 following transplantation.Lung metastasis,MD SC recruitment,the expression of PMN and S1PR1/STAT3 axis biomarkers,as well as the blood levels of granulocyte-mac rophage colony-stimulating factor(GM-CSF) and transforming growth factor-β(TGF-β) were assessed in the SSG treatment and control groups.Results:The LLC cells did not reach the lung until 14-17 days following subcutaneous implantation,which was concurrent with the formation of lung PMNs.S SG significantly postponed the initiation of lung metastasis and reduced the recruitment of MDSCs to the lung PMNs.S SG also suppre ssed the S1PR1/STAT3 axis in tumor tissue s,bone marrow,and lung PMNs.Additionally,SSG suppres sed the blood levels of GM-CSF and TGF-β,as well as the PMN markers,matrix metalloproteinase-9 and versican.Conclusion:Our findings suggested that SSG suppressed the development of MD SC-mediated PMNs by inhibiting the S1PR1/STAT3 axis,consequently postponing the initiation of lung metastasis.
基金supported by the China’s 14th Five-Year Plan National Key Research and Development Program“Marine Agriculture and Freshwater Fisheries Science and Technology Innovation”Key Special Project(2024YFD2402203)Foreign Experts Program of the Ministry of Science and Technology(S20240181),the Innovation Program of Shanghai Municipal Education Commission(2023ZKZD52)the Open Research Fund of State Key Laboratory of Estuarine and Coastal Research(SKLEC-KF202309)。
文摘The biodegradable plastic poly(lactic acid)(PLA)has been widely used to reduce plastic pollution in the environment,but PLA does not readily degrade completely and is more prone to form microplastics(MPs)and age.In this study,MP-PLA was aged by simulating the behavior of the marine environment and combined with plastic additive tris(1-chloro-2-propyl)phosphate(TCPP)according to their susceptibility to adsorb environmental pollutants.Mussels were the exposed subjects,and exposure concentrations of MPs and TCPP were set at 0.2 mg/L,1 mg/L,and 0.5μg/L,respectively.The ecotoxicity of PLA,aged-PLA,TCPP,and TCPP+aged-PLA was compared based on the result that aged-PLA could adsorb more TCPP.Biomarker assays revealed that mussels ingesting and accumulating contaminants underwent a severe oxidative(ROS)and immune stress response in the organism,with disruption of energy metabolism for energy supply,leading to apoptosis,resulting in tissue damage,and disruption of the homeostasis of the symbiotic intestinal microbiota.Comparisons showed that aging enhanced the adverse effects of PLA and ecotoxicological effects are further exacerbated by the adsorption of TCPP on aged-PLA.Therefore,with the widespread use of degradable plastics,long-term environmental impacts such as incomplete degradation and release of additives must be a concern.
