Human experts cannot efficiently access physical information of a quantum many-body states by simply "reading"its coefficients, but have to reply on the previous knowledge such as order parameters and quantu...Human experts cannot efficiently access physical information of a quantum many-body states by simply "reading"its coefficients, but have to reply on the previous knowledge such as order parameters and quantum measurements.We demonstrate that convolutional neural network(CNN) can learn from coefficients of many-body states or reduced density matrices to estimate the physical parameters of the interacting Hamiltonians, such as coupling strengths and magnetic fields, provided the states as the ground states. We propose QubismNet that consists of two main parts: the Qubism map that visualizes the ground states(or the purified reduced density matrices) as images, and a CNN that maps the images to the target physical parameters. By assuming certain constraints on the training set for the sake of balance, QubismNet exhibits impressive powers of learning and generalization on several quantum spin models. While the training samples are restricted to the states from certain ranges of the parameters, QubismNet can accurately estimate the parameters of the states beyond such training regions. For instance, our results show that QubismNet can estimate the magnetic fields near the critical point by learning from the states away from the critical vicinity. Our work provides a data-driven way to infer the Hamiltonians that give the designed ground states, and therefore would benefit the existing and future generations of quantum technologies such as Hamiltonian-based quantum simulations and state tomography.展开更多
Aging biomarkers are a combination of biological parameters to(i)assess age-related changes,(ii)track the physiological aging process,and(iii)predict the transition into a pathological status.Although a broad spectrum...Aging biomarkers are a combination of biological parameters to(i)assess age-related changes,(ii)track the physiological aging process,and(iii)predict the transition into a pathological status.Although a broad spectrum of aging biomarkers has been developed,their potential uses and limitations remain poorly characterized.An immediate goal of biomarkers is to help us answer the following three fundamental questions in aging research:How old are we?Why do we get old?And how can we age slower?This review aims to address this need.Here,we summarize our current knowledge of biomarkers developed for cellular,organ,and organismal levels of aging,comprising six pillars:physiological characteristics,medical imaging,histological features,cellular alterations,molecular changes,and secretory factors.To fulfill all these requisites,we propose that aging biomarkers should qualify for being specific,systemic,and clinically relevant.展开更多
As one of the main tumor-infiltrating immune cell types, tumor-associated macrophages (TAMs) determine the efficacy of immunotherapy. However, limited knowledge about their phenotypically and functionally heterogeneou...As one of the main tumor-infiltrating immune cell types, tumor-associated macrophages (TAMs) determine the efficacy of immunotherapy. However, limited knowledge about their phenotypically and functionally heterogeneous nature restricts their application in tumor immunotherapy. In this study, we identified a subpopulation of CD146+ TAMs that exerted antitumor activity in both human samples and animal models. CD146 expression in TAMs was negatively controlled by STAT3 signaling. Reducing this population of TAMs promoted tumor development by facilitating myeloid-derived suppressor cell recruitment via activation of JNK signaling. Interestingly, CD146 was involved in the NLRP3 inflammasome-mediated activation of macrophages in the tumor microenvironment, partially by inhibiting transmembrane protein 176B (TMEM176B), an immunoregulatory cation channel. Treatment with a TMEM176B inhibitor enhanced the antitumor activity of CD146+ TAMs. These data reveal a crucial antitumor role of CD146+ TAMs and highlight the promising immunotherapeutic approach of inhibiting CD146 and TMEM176B.展开更多
Tissue-resident macrophages are derived from different precursor cells and display different phenotypes.Reconstitution of the tissue-resident macrophages of inflamed or damaged tissues in adults can be achieved by bon...Tissue-resident macrophages are derived from different precursor cells and display different phenotypes.Reconstitution of the tissue-resident macrophages of inflamed or damaged tissues in adults can be achieved by bone marrow-derived monocytes/macrophages.Using lysozyme(Lysm)-GFP-reporter mice,we found that alveolar macrophages(AMs),Kupffer cells,red pulp macrophages(RpMacs),and kidney-resident macrophages were Lysm-GFP^(−),whereas all monocytes in the fetal liver,adult bone marrow,and blood were Lysm-GFP^(+).Donor-derived Lysm-GFP^(+)resident macrophages gradually became Lysm-GFP−in recipients and developed gene expression profiles characteristic of tissue-resident macrophages.Thus,Lysm may be used to distinguish newly formed and long-term surviving tissue-resident macrophages that were derived from bone marrow precursor cells in adult mice under pathological conditions.Furthermore,we found that Irf4 might be essential for resident macrophage differentiation in all tissues,while cytokine and receptor pathways,mTOR signaling pathways,and fatty acid metabolic processes predominantly regulated the differentiation of RpMacs,Kupffer cells,and kidney macrophages,respectively.Deficiencies in ST2,mechanistic target of rapamycin(mTOR)and fatty acid-binding protein 5(FABP5)differentially impaired the differentiation of tissue-resident macrophages from bone marrow-derived monocytes/macrophages in the lungs,liver,and kidneys.These results indicate that a combination of shared and unique signaling pathways coordinately shape tissue-resident macrophage differentiation in various tissues.展开更多
In the electronic information and intelligent era, microwave absorption materials have been focused on the issue of electromagnetic(EM) pollution, but high-performance absorbers with thin thickness are highly desirabl...In the electronic information and intelligent era, microwave absorption materials have been focused on the issue of electromagnetic(EM) pollution, but high-performance absorbers with thin thickness are highly desirable. The positive action between structural design and component selection can be regarded as a function to optimize the microwave loss capacity, which contributes to understanding the response mechanisms from the micro and macro. Therefore, we designed the absorber with quasiperiodic structures of Penrose tiling that has finely engineered the location of maximum absorption peak, the spherical carbonyl iron in thin rhombus, and flakey carbonyl iron in fat rhombus, the effective absorption bandwidth(Reflection Loss ≤ –10 d B) was realized from 6.46 GHz to 15.78 GHz in the 2 mm thickness. The unique arrangement of Penrose tiling can respond alternatingly to EM waves at large scales, and multicomponent coupling is distinctly in the neighboring unit cells. In addition, spraying aluminum pigment as the upper layer, the infrared emissivity is less than 0.35 to meet the complex application environment.This work opens up novel ideas on quasiperiodic structure combined multicomponent and injects infinite vitality to provide prospects for broadband responsive and high-efciency EM absorbers.展开更多
Since its identification as a marker for advanced melanoma in the 1980s,CD146 has been found to have multiple functions in both physiological and pathological processes,including embryonic development,tissue repair an...Since its identification as a marker for advanced melanoma in the 1980s,CD146 has been found to have multiple functions in both physiological and pathological processes,including embryonic development,tissue repair and regeneration,tumor progression,fibrosis disease,and inflammations.Subsequent research has revealed that CD146 is involved in various signaling pathways as a receptor or coreceptor in these processes.This correlation between CD146 and multiple diseases has sparked interest in its potential applications in diagnosis,prognosis,and targeted therapy.To better comprehend the versatile roles of CD146,we have summarized its research history and synthesized findings from numerous reports,proposing that cell plasticity serves as the underlying mechanism through which CD146 contributes to development,regeneration,and various diseases.Targeting CD146 would consequently halt cell state shifting during the onset and progression of these related diseases.Therefore,the development of therapy targeting CD146 holds significant practical value.展开更多
Pork meat is closely related to physicochemical alterations during growth and development,resulting in differences in nutritional value and meat flavor.This study aimed to evaluate the composition of amino acids,fatty...Pork meat is closely related to physicochemical alterations during growth and development,resulting in differences in nutritional value and meat flavor.This study aimed to evaluate the composition of amino acids,fatty acids,and metabolic profiles in the longissimus thoracis muscle(LM)of Shaziling pigs aged 30,90,150,210,and 300 days.The results showed that the predominant fatty acids identified in the LM of Shaziling pigs were C16:0,C16:1,C18:0,C18:1n9c,and C18:2n6c.An opposite correlation was observed for C18:2n6c and n6/n3 polyunsaturated fatty acids(P<0.05).Alanine,aspartate,glutamate,Dglutamine,and D-glutamate metabolism were the main metabolic pathways for the Shaziling pig meat flavor(P<0.05).Moreover,the correlation coefficients revealed that the contents of anserine,C16:0,C16:1,and C18:1n9c were positively correlated with intramuscular fat and/or p H24hand were negatively correlated with the values of L^(*)(lightness)and b^(*)(yellowness)(P<0.05).In conclusion,age greatly affected the meat quality of Shaziling pigs,and the contents of muscular anserine,C16:0,C16:1,and C18:1n9c might be promising indicators for better meat quality.展开更多
Beige fat,a newly discovered adipose tissue featuring high functional flexibility,exhibits the characteristics of white fat at rest,but can be activated to function like brown fat under cold or β-adrenergic stimulati...Beige fat,a newly discovered adipose tissue featuring high functional flexibility,exhibits the characteristics of white fat at rest,but can be activated to function like brown fat under cold or β-adrenergic stimulation via a process termed‘browning of white fat’.This activation enables beige fat to greatly promote heat production and energy consumption,as well as to improve systemic glucose and lipid metabolism.Beige fat also exists in supraclavicular and paraspinal regions in human adults,which endows its great potential forintervention ofobesityandmetabolic diseases.展开更多
Non-alcoholic fatty liver disease(NAFLD)is a common chronic disease characterized by excessive fat accumulation in hepatocytes in the absence of alcohol consumption.Modern trends towards excessive calorie intake and s...Non-alcoholic fatty liver disease(NAFLD)is a common chronic disease characterized by excessive fat accumulation in hepatocytes in the absence of alcohol consumption.Modern trends towards excessive calorie intake and sedentary life styles have increased the prevalence of NAFLD accompanied by obesity and type 2 diabetes.However,the molecular mechanisms underlying the initiation and progression of NAFLD are not clear.Zinc finger proteins(ZFPs)are a superfamily of metalloproteins that contain zinc finger motifs.ZFPs play diverse physiological roles in tissue homeostasis and also contribute to many pathological conditions,including metabolic,cardiovascular,and neurodegenerative diseases and various types of cancer.In this review,we highlight our current knowledge of several ZFPs that play critical roles in the progression of NAFLD,describe their mechanistic functional networks,and discuss the potential for ZFPs as therapeutic targets for NAFLD.展开更多
基金Supported by the National Natural Science Foundation of China (Grant Nos. 12004266, 11834014 and 11975050)the Beijing Natural Science Foundation (Grant Nos. 1192005 and Z180013)+1 种基金the Foundation of Beijing Education Committees (Grant No.KM202010028013)the Academy for Multidisciplinary Studies,Capital Normal University。
文摘Human experts cannot efficiently access physical information of a quantum many-body states by simply "reading"its coefficients, but have to reply on the previous knowledge such as order parameters and quantum measurements.We demonstrate that convolutional neural network(CNN) can learn from coefficients of many-body states or reduced density matrices to estimate the physical parameters of the interacting Hamiltonians, such as coupling strengths and magnetic fields, provided the states as the ground states. We propose QubismNet that consists of two main parts: the Qubism map that visualizes the ground states(or the purified reduced density matrices) as images, and a CNN that maps the images to the target physical parameters. By assuming certain constraints on the training set for the sake of balance, QubismNet exhibits impressive powers of learning and generalization on several quantum spin models. While the training samples are restricted to the states from certain ranges of the parameters, QubismNet can accurately estimate the parameters of the states beyond such training regions. For instance, our results show that QubismNet can estimate the magnetic fields near the critical point by learning from the states away from the critical vicinity. Our work provides a data-driven way to infer the Hamiltonians that give the designed ground states, and therefore would benefit the existing and future generations of quantum technologies such as Hamiltonian-based quantum simulations and state tomography.
基金supported by the National Natural Science Foundation of China(31730036,31871380,31871382,31930055,31930058,32000500,32022034,32030033,32070730,32130046,3217050247,32150005,32200595,32222024,81730019,81730022,81830014,81921006,81925005,81970426,81971301,81971312,82030041,82061160495,82070805,82071595,82090020,82100841,82120108009,82122024,82125002,82125011,82125012,82130045,82171284,82173061,82173398,82225007,82225015,82225017,82225018,82230047,82230088,82271600,91949106,91949201,92049116,92049302,92049304,92149303,92149306,92157202,92168201,92169102,92249301,92268201)the National Key Research and Development Program of China(2018YFA0800700,2018YFC2000100,2018YFC2000102,2018YFC2002003,2019YFA0110900,2019YFA0801703,2019YFA0801903,2019YFA0802202,2019YFA0904800,2020YFA0113400,2020YFA0803401,2020YFA0804000,2020YFC2002900,2020YFC2008000,2020YFE0202200,2021YFA0804900,2021YFA1100103,2021YFA1100900,2021YFE0114200,2021ZD0202400,2022YFA0806001,2022YFA0806002,2022YFA0806600,2022YFA1103200,2022YFA1103601,2022YFA1103701,2022YFA1103800,2022YFA1103801,2022YFA1104100,2022YFA1104904,2022YFA1303000,2022YFC2009900,2022YFC2502401,2022YFC3602400,2022YFE0118000,2022ZD0213200)+14 种基金the Strategic Priority Research Program of the Chinese Academy of Sciences(XDA16030302,XDB39000000,XDB39030600)the Youth Innovation Promotion Association of Chinese Academy of Sciences(2020085,2021080)CAS Project for Young Scientists in Basic Research(YSBR-076)the Program of the Beijing Natural Science Foundation(JQ20031)Clinical Research Operating Fund of Central High level hospitals(2022-PUMCHE-001)CAMS Innovation Fund for Medical Sciences(CIFMS)(2022-I2M1-004)Talent Program of the Chinese Academy of Medical Science(2022RC310-10)Research Funds from Health@Inno HK Program launched by Innovation Technology Commission of the Hong Kong Special Administrative Region,Guangdong Basic and Applied Basic Research Foundation(2020B1515020044)Guangzhou Planned Project of Science and Technology(202002020039)the Major Technology Innovation of Hubei Province(2019ACA141)the Science and Technology Major Project of Hunan Provincial Science and Technology Department(2021SK1010)Shanghai Municipal Science and Technology Major Project(2017SHZDZX01)the Natural Science Foundation of Sichuan Province(2023NSFSC0003)Yunnan Fundamental Research Project(202201AS070080)the State Key Laboratory of Membrane Biology。
文摘Aging biomarkers are a combination of biological parameters to(i)assess age-related changes,(ii)track the physiological aging process,and(iii)predict the transition into a pathological status.Although a broad spectrum of aging biomarkers has been developed,their potential uses and limitations remain poorly characterized.An immediate goal of biomarkers is to help us answer the following three fundamental questions in aging research:How old are we?Why do we get old?And how can we age slower?This review aims to address this need.Here,we summarize our current knowledge of biomarkers developed for cellular,organ,and organismal levels of aging,comprising six pillars:physiological characteristics,medical imaging,histological features,cellular alterations,molecular changes,and secretory factors.To fulfill all these requisites,we propose that aging biomarkers should qualify for being specific,systemic,and clinically relevant.
基金supported in part by grants from the Beijing Natural Science Foundation of China(Grant No.7192123,7222117)the National Natural Science Foundation of China(Grant No.31770793,82000812)the Youth Innovation Promotion Association of Chinese Academy of Sciences(Grant No.2018122).
文摘As one of the main tumor-infiltrating immune cell types, tumor-associated macrophages (TAMs) determine the efficacy of immunotherapy. However, limited knowledge about their phenotypically and functionally heterogeneous nature restricts their application in tumor immunotherapy. In this study, we identified a subpopulation of CD146+ TAMs that exerted antitumor activity in both human samples and animal models. CD146 expression in TAMs was negatively controlled by STAT3 signaling. Reducing this population of TAMs promoted tumor development by facilitating myeloid-derived suppressor cell recruitment via activation of JNK signaling. Interestingly, CD146 was involved in the NLRP3 inflammasome-mediated activation of macrophages in the tumor microenvironment, partially by inhibiting transmembrane protein 176B (TMEM176B), an immunoregulatory cation channel. Treatment with a TMEM176B inhibitor enhanced the antitumor activity of CD146+ TAMs. These data reveal a crucial antitumor role of CD146+ TAMs and highlight the promising immunotherapeutic approach of inhibiting CD146 and TMEM176B.
基金supported by grants from the National Natural Science Foundation for Key Programs (31930041,Y.Z.)National Key Research and Development Program of China (2017YFA0105002,2017YFA0104402,Y.Z.)Knowledge Innovation Program of the Chinese Academy of Sciences (XDA16030301,Y.Z.).
文摘Tissue-resident macrophages are derived from different precursor cells and display different phenotypes.Reconstitution of the tissue-resident macrophages of inflamed or damaged tissues in adults can be achieved by bone marrow-derived monocytes/macrophages.Using lysozyme(Lysm)-GFP-reporter mice,we found that alveolar macrophages(AMs),Kupffer cells,red pulp macrophages(RpMacs),and kidney-resident macrophages were Lysm-GFP^(−),whereas all monocytes in the fetal liver,adult bone marrow,and blood were Lysm-GFP^(+).Donor-derived Lysm-GFP^(+)resident macrophages gradually became Lysm-GFP−in recipients and developed gene expression profiles characteristic of tissue-resident macrophages.Thus,Lysm may be used to distinguish newly formed and long-term surviving tissue-resident macrophages that were derived from bone marrow precursor cells in adult mice under pathological conditions.Furthermore,we found that Irf4 might be essential for resident macrophage differentiation in all tissues,while cytokine and receptor pathways,mTOR signaling pathways,and fatty acid metabolic processes predominantly regulated the differentiation of RpMacs,Kupffer cells,and kidney macrophages,respectively.Deficiencies in ST2,mechanistic target of rapamycin(mTOR)and fatty acid-binding protein 5(FABP5)differentially impaired the differentiation of tissue-resident macrophages from bone marrow-derived monocytes/macrophages in the lungs,liver,and kidneys.These results indicate that a combination of shared and unique signaling pathways coordinately shape tissue-resident macrophage differentiation in various tissues.
基金Supported by Program for the National Natural Science Foundation of China (Nos.52103334,52071053,U1704253)the China Postdoctoral Science Foundation(Nos.2020M680946,2020M670748)the Fundamental Research Funds for the Central Universities (No.DUT20GF111)。
文摘In the electronic information and intelligent era, microwave absorption materials have been focused on the issue of electromagnetic(EM) pollution, but high-performance absorbers with thin thickness are highly desirable. The positive action between structural design and component selection can be regarded as a function to optimize the microwave loss capacity, which contributes to understanding the response mechanisms from the micro and macro. Therefore, we designed the absorber with quasiperiodic structures of Penrose tiling that has finely engineered the location of maximum absorption peak, the spherical carbonyl iron in thin rhombus, and flakey carbonyl iron in fat rhombus, the effective absorption bandwidth(Reflection Loss ≤ –10 d B) was realized from 6.46 GHz to 15.78 GHz in the 2 mm thickness. The unique arrangement of Penrose tiling can respond alternatingly to EM waves at large scales, and multicomponent coupling is distinctly in the neighboring unit cells. In addition, spraying aluminum pigment as the upper layer, the infrared emissivity is less than 0.35 to meet the complex application environment.This work opens up novel ideas on quasiperiodic structure combined multicomponent and injects infinite vitality to provide prospects for broadband responsive and high-efciency EM absorbers.
基金supported in part by the Beijing Natural Science Foundation of China(L232077,7242092,7222117)the National Natural Science Foundation of China(82000812)the China Postdoctoral Science Foundation(2023M733682).
文摘Since its identification as a marker for advanced melanoma in the 1980s,CD146 has been found to have multiple functions in both physiological and pathological processes,including embryonic development,tissue repair and regeneration,tumor progression,fibrosis disease,and inflammations.Subsequent research has revealed that CD146 is involved in various signaling pathways as a receptor or coreceptor in these processes.This correlation between CD146 and multiple diseases has sparked interest in its potential applications in diagnosis,prognosis,and targeted therapy.To better comprehend the versatile roles of CD146,we have summarized its research history and synthesized findings from numerous reports,proposing that cell plasticity serves as the underlying mechanism through which CD146 contributes to development,regeneration,and various diseases.Targeting CD146 would consequently halt cell state shifting during the onset and progression of these related diseases.Therefore,the development of therapy targeting CD146 holds significant practical value.
基金jointly supported by the National Natural Science Foundation of China (U19A2037)the Changsha Natural Science Funds for Distinguished Young Scholars (kq2009020)+6 种基金Young Elite Scientists Sponsorship Program by CAST (2020-2022QNRC003)the Natural Science Foundation of Hunan Province (2021JJ20044)the Natural Science Foundation of Guangxi Province (2020JJA130102)China Agriculture Research System of MOF and MARA (CARS-35)the Strategic Priority Research Program of the Chinese Academy of Sciences (XDA24030204)the National Key Research and Development Program of China (2022YFD1300503)the Science and Technology Innovation Program of Hunan Province (2022RC1159)。
文摘Pork meat is closely related to physicochemical alterations during growth and development,resulting in differences in nutritional value and meat flavor.This study aimed to evaluate the composition of amino acids,fatty acids,and metabolic profiles in the longissimus thoracis muscle(LM)of Shaziling pigs aged 30,90,150,210,and 300 days.The results showed that the predominant fatty acids identified in the LM of Shaziling pigs were C16:0,C16:1,C18:0,C18:1n9c,and C18:2n6c.An opposite correlation was observed for C18:2n6c and n6/n3 polyunsaturated fatty acids(P<0.05).Alanine,aspartate,glutamate,Dglutamine,and D-glutamate metabolism were the main metabolic pathways for the Shaziling pig meat flavor(P<0.05).Moreover,the correlation coefficients revealed that the contents of anserine,C16:0,C16:1,and C18:1n9c were positively correlated with intramuscular fat and/or p H24hand were negatively correlated with the values of L^(*)(lightness)and b^(*)(yellowness)(P<0.05).In conclusion,age greatly affected the meat quality of Shaziling pigs,and the contents of muscular anserine,C16:0,C16:1,and C18:1n9c might be promising indicators for better meat quality.
文摘Beige fat,a newly discovered adipose tissue featuring high functional flexibility,exhibits the characteristics of white fat at rest,but can be activated to function like brown fat under cold or β-adrenergic stimulation via a process termed‘browning of white fat’.This activation enables beige fat to greatly promote heat production and energy consumption,as well as to improve systemic glucose and lipid metabolism.Beige fat also exists in supraclavicular and paraspinal regions in human adults,which endows its great potential forintervention ofobesityandmetabolic diseases.
基金This work was supported by funds from the National Natural Science Foundation of China(31770840 to X.Ma and 31800989 to L.Xu)the Program for Professor of Special Appointment(Eastern Scholar)at Shanghai Institutions of Higher Learning(TP2017042 to X.Ma)。
文摘Non-alcoholic fatty liver disease(NAFLD)is a common chronic disease characterized by excessive fat accumulation in hepatocytes in the absence of alcohol consumption.Modern trends towards excessive calorie intake and sedentary life styles have increased the prevalence of NAFLD accompanied by obesity and type 2 diabetes.However,the molecular mechanisms underlying the initiation and progression of NAFLD are not clear.Zinc finger proteins(ZFPs)are a superfamily of metalloproteins that contain zinc finger motifs.ZFPs play diverse physiological roles in tissue homeostasis and also contribute to many pathological conditions,including metabolic,cardiovascular,and neurodegenerative diseases and various types of cancer.In this review,we highlight our current knowledge of several ZFPs that play critical roles in the progression of NAFLD,describe their mechanistic functional networks,and discuss the potential for ZFPs as therapeutic targets for NAFLD.