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1.
Hum Mol Genet ; 32(14): 2347-2356, 2023 07 04.
Artigo em Inglês | MEDLINE | ID: mdl-37162351

RESUMO

Medium-chain acyl-CoA dehydrogenase (MCAD) deficiency is the most common inherited disorder of mitochondrial fatty acid ß-oxidation (FAO) in humans. Patients exhibit clinical episodes often associated with fasting. Symptoms include hypoketotic hypoglycemia and Reye-like episodes. With limited treatment options, we explored the use of human MCAD (hMCAD) mRNA in fibroblasts from patients with MCAD deficiency to provide functional MCAD protein and reverse the metabolic block. Transfection of hMCAD mRNA into MCAD- deficient patient cells resulted in an increased MCAD protein that localized to mitochondria, concomitant with increased enzyme activity in cell extracts. The therapeutic hMCAD mRNA-lipid nanoparticle (LNP) formulation was also tested in vivo in Acadm-/- mice. Administration of multiple intravenous doses of the hMCAD mRNA-LNP complex (LNP-MCAD) into Acadm-/- mice produced a significant level of MCAD protein with increased enzyme activity in liver, heart and skeletal muscle homogenates. Treated Acadm-/- mice were more resistant to cold stress and had decreased plasma levels of medium-chain acylcarnitines compared to untreated animals. Furthermore, hepatic steatosis in the liver from treated Acadm-/- mice was reduced compared to untreated ones. Results from this study support the potential therapeutic value of hMCAD mRNA-LNP complex treatment for MCAD deficiency.


Assuntos
Acil-CoA Desidrogenases , Fibroblastos , Humanos , Camundongos , Animais , Acil-CoA Desidrogenase/genética , Acil-CoA Desidrogenase/metabolismo , RNA Mensageiro/genética , Modelos Animais de Doenças , Fibroblastos/metabolismo
2.
Cell Mol Life Sci ; 81(1): 76, 2024 Feb 05.
Artigo em Inglês | MEDLINE | ID: mdl-38315203

RESUMO

Metastatic cancer is a major cause of cancer-related mortality; however, the complex regulation process remains to be further elucidated. A large amount of preliminary investigations focus on the role of epigenetic mechanisms in cancer metastasis. Notably, the posttranslational modifications were found to be critically involved in malignancy, thus attracting considerable attention. Beyond acetylation, novel forms of acylation have been recently identified following advances in mass spectrometry, proteomics technologies, and bioinformatics, such as propionylation, butyrylation, malonylation, succinylation, crotonylation, 2-hydroxyisobutyrylation, lactylation, among others. These novel acylations play pivotal roles in regulating different aspects of energy mechanism and mediating signal transduction by covalently modifying histone or nonhistone proteins. Furthermore, these acylations and their modifying enzymes show promise regarding the diagnosis and treatment of tumors, especially tumor metastasis. Here, we comprehensively review the identification and characterization of 11 novel acylations, and the corresponding modifying enzymes, highlighting their significance for tumor metastasis. We also focus on their potential application as clinical therapeutic targets and diagnostic predictors, discussing the current obstacles and future research prospects.


Assuntos
Histonas , Neoplasias , Humanos , Acilação , Histonas/metabolismo , Acetilação , Processamento de Proteína Pós-Traducional , Neoplasias/genética
3.
Anal Chem ; 96(12): 4891-4900, 2024 03 26.
Artigo em Inglês | MEDLINE | ID: mdl-38462674

RESUMO

Lateral flow immunoassay (LFIA), a classical point-of-care testing (POCT) technique, plays an important role in disease screening and healthcare monitoring. However, traditional LFIA is either designed for qualitative analysis or requires expensive equipment for quantification, limiting its use in household diagnosis. In this study, we proposed a new generation of LFIA for household health monitoring by using ultralong organic phosphorescence (UOP) nanomaterials as afterglow nanoprobes with a self-developed palm-size sensing device. The UOP nanoprobes exhibit a phosphorescence signal with a second-level lifetime, which completely avoids the interference from excitation light and biological background fluorescence. Therefore, an ultraminiaturized and low-cost UOP nanosensor was successfully designed by eliminating the complex optical path and filtering systems. We chose an inflammatory factor, C-reactive protein (CRP), for household POCT validation. The whole analysis was completed within 9 min. A limit of detection (LOD) of 0.54 ng/mL of CRP antigen was achieved with high stability and good specificity, which is comparable to laboratory instruments and fully satisfying the clinical diagnosis requirement.


Assuntos
Nanoestruturas , Imunoensaio/métodos , Limite de Detecção
4.
Ecotoxicol Environ Saf ; 284: 116865, 2024 Oct 01.
Artigo em Inglês | MEDLINE | ID: mdl-39137461

RESUMO

Tebuconazole (TEB), a prominent chiral triazole fungicide, has been extensively utilized for plant pathogen control globally. Despite experimental evidence of TEB metabolism in mammals, the enantioselectivity in the biotransformation of R- and S-TEB enantiomers by specific CYP450s remains elusive. In this work, integrated in silico simulations were employed to unveil the binding interactions and enantioselective metabolic fate of TEB enantiomers within human CYP1A2, 2B6, 2E1, and 3A4. Molecular dynamics (MD) simulations clearly delineated the binding specificity of R- and S-TEB to the four CYP450s, crucially determining their differences in metabolic activity and enantioselectivity. The primary driving force for robust ligand binding was identified as van der Waals interactions with CYP450s, particularly involving the hydrophobic residues. Mechanistic insights derived from quantum mechanics/molecular mechanics (QM/MM) calculations established C2-methyl hydroxylation as the predominant route of R-/S-TEB metabolism, while C6-hydroxylation and triazol epoxidation were deemed kinetically infeasible pathways. Specifically, the resulting hydroxy-R-TEB metabolite primarily originates from R-TEB biotransformation by 1A2, 2E1 and 3A4, whereas hydroxy-S-TEB is preferentially produced by 2B6. These findings significantly contribute to our comprehension of the binding specificity and enantioselective metabolic fate of chiral TEB by CYP450s, potentially informing further research on human health risk assessment associated with TEB exposure.


Assuntos
Sistema Enzimático do Citocromo P-450 , Fungicidas Industriais , Simulação de Dinâmica Molecular , Triazóis , Triazóis/química , Triazóis/metabolismo , Fungicidas Industriais/química , Fungicidas Industriais/metabolismo , Humanos , Sistema Enzimático do Citocromo P-450/metabolismo , Estereoisomerismo , Simulação por Computador , Citocromo P-450 CYP1A2/metabolismo , Citocromo P-450 CYP1A2/química , Citocromo P-450 CYP2B6/metabolismo , Citocromo P-450 CYP2B6/química , Biotransformação , Citocromo P-450 CYP2E1/metabolismo , Citocromo P-450 CYP2E1/química , Citocromo P-450 CYP3A/metabolismo
5.
Angew Chem Int Ed Engl ; 63(14): e202319694, 2024 Apr 02.
Artigo em Inglês | MEDLINE | ID: mdl-38314961

RESUMO

Organic phosphors offer a promising alternative in optoelectronics, but their temperature-sensitive feature has restricted their applications in high-temperature scenarios, and the attainment of high-temperature phosphorescence (HTP) is still challenging. Herein, a series of organic cocrystal phosphors are constructed by supramolecular assembly with an ultralong emission lifetime of up to 2.16 s. Intriguingly, remarkable stabilization of triplet excitons can also be realized at elevated temperature, and green phosphorescence is still exhibited in solid state even up to 150 °C. From special molecular packing within the crystal lattice, it has been observed that the orientation of isolated water cluster and well-controlled molecular organization via multiple interactions can favor the structural rigidity of cocrystals more effectively to suppress the nonradiative transition, thus resulting in efficient room-temperature phosphorescence and unprecedented survival of HTP.

6.
Small ; 19(31): e2207104, 2023 Aug.
Artigo em Inglês | MEDLINE | ID: mdl-36810867

RESUMO

Carbon dots (CDs) have gradually become a new generation of nano-luminescent materials, which have received extensive attention due to excellent optical properties, wide source of raw materials, low toxicity, and good biocompatibility. In recent years, there are many reports on the luminescent phenomenon of CDs, and great progress has been achieved. However,there are rarely systematic summaries on CDs with persistent luminescence. Here, a summary of the recent progress on persistent luminescent CDs, including luminous mechanism, synthetic strategies, property regulation, and potential applications, is given. First, a brief introduction is given to the development of CDs luminescent materials. Then, the luminous mechanism of afterglow CDs from room temperature phosphorescence (RTP), delayed fluorescence (DF), and long persistent luminescence (LPL) is discussed. Next, the constructed methods of luminescent CDs materials are summarized from two aspects, including matrix-free self-protected and matrix-protected CDs. Moreover, the regulation of afterglow properties from color, lifetime, and efficiency is presented. Afterwards, the potential applications of CDs, such as anti-counterfeiting, information encryption, sensing, bio-imaging, multicolor display, LED devices, etc., are reviewed. Finally, an outlook on the development of CDs materials and applications is proposed.

7.
Mol Genet Metab ; 138(1): 106982, 2023 01.
Artigo em Inglês | MEDLINE | ID: mdl-36580829

RESUMO

Very long-chain acyl-CoA dehydrogenase (VLCAD) deficiency is an inborn error of long chain fatty acid ß-oxidation (FAO) with limited treatment options. Patients present with heterogeneous clinical phenotypes affecting predominantly heart, liver, and skeletal muscle. While VLCAD deficiency is a systemic disease, restoration of liver FAO has the potential to improve symptoms more broadly due to increased total body ATP production and reduced accumulation of potentially toxic metabolites. We explored the use of synthetic human VLCAD (hVLCAD) mRNA and lipid nanoparticle encapsulated hVLCAD mRNA (LNP-VLCAD) to generate functional VLCAD enzyme in patient fibroblasts derived from VLCAD deficient patients, mouse embryonic fibroblasts, hepatocytes isolated from VLCAD knockout (Acadvl-/-) mice, and Acadvl-/- mice to reverse the metabolic effects of the deficiency. Transfection of all cell types with hVLCAD mRNA resulted in high level expression of protein that localized to mitochondria with increased enzyme activity. Intravenous administration of LNP-VLCAD to Acadvl-/- mice produced a significant amount of VLCAD protein in liver, which declined over a week. Treated Acadvl-/- mice showed reduced hepatic steatosis, were more resistant to cold stress, and accumulated less toxic metabolites in blood than untreated animals. Results from this study support the potential for hVLCAD mRNA for treatment of VLCAD deficiency.


Assuntos
Acil-CoA Desidrogenase de Cadeia Longa , Erros Inatos do Metabolismo Lipídico , Humanos , Animais , Camundongos , RNA Mensageiro/genética , RNA Mensageiro/metabolismo , Modelos Animais de Doenças , Fibroblastos/metabolismo , Erros Inatos do Metabolismo Lipídico/genética , Erros Inatos do Metabolismo Lipídico/terapia
8.
Acc Chem Res ; 55(23): 3445-3459, 2022 12 06.
Artigo em Inglês | MEDLINE | ID: mdl-36368944

RESUMO

Organic phosphorescence is defined as a radiative transition between the different spin multiplicities of an organic molecule after excitation; here, we refer to the photoexcitation. Unlike fluorescence, it shows a long emission lifetime (∼µs), large Stokes shift, and rich excited state properties, attracting considerable attention in organic electronics during the past years. Ultralong organic phosphorescence (UOP), a type of persistent luminescence in organic phosphors, shows an emission lifetime of over 100 ms normally according to the resolution limit of the naked eye. According to the Jablonski energy diagram, two prerequisites are necessary for UOP generation and enhancement. One is to promote intersystem crossing (ISC) of the excitons from the excited singlet to triplet states by enhancing the spin-orbit coupling (SOC); the other is to suppress the nonradiative transitions of the excitons from the excited triplet states.In this Account, we will give a summary of our research on ultralong organic phosphorescence, including the design of materials, manipulation of properties, fabrication of nano/microstructures, and function applications. First, we give a brief introduction to the UOP development. Then, we discuss the constructed methods of UOP materials from the inter/intramolecular interaction types, including π-π interactions, intermolecular hydrogen bonds, halogen bonds, ionic bonds, covalent bonds, and so on. These effective interactions can build a rigid environment to restrain the nonradiative transitions from the molecular motions or external quenching by oxygen, moisture, or heat, and thus enhance the UOP performance. Next, the manipulation of UOP properties, containing excitation wavelength, emission colors, lifetimes, and quantum efficiency (QE), through molecular or crystal engineering will be summarized. Recently, the excitation wavelengths of the materials for UOP can be regulated in different regions, such as UV, visible light, and X-ray; the emission colors of UOP can cover the whole visible-light region, from deep blue to red; the phosphorescence lifetime of UOP materials can reach 2.5 s, and the quantum efficiency can be achieved up to 96.5%. Moreover, we will present the fabrication of micro/nanoscale UOP materials, including the preparation of micro/nanostructure, optical performance, and device fabrication. Afterward, we will review the potential applications of UOP materials in organic/bio-optoelectronics, such as information encryption, bioimaging, sensing, afterglow display, etc. Finally, an outlook on the development of UOP materials and applications will be proposed.

9.
Angew Chem Int Ed Engl ; 62(24): e202301564, 2023 Jun 12.
Artigo em Inglês | MEDLINE | ID: mdl-37026975

RESUMO

Dynamic room temperature phosphorescence (RTP) materials have potential applications in optoelectronics, which inevitably suffer from poor processability, flexibility or stretchability. Herein, we report a concise strategy to develop supercooled liquids (SCLs) with dynamic RTP behavior using terminal hydroxyl engineering. The terminal hydroxyls effectively hinder the nucleation process of molecules for the formation of stable SCLs after thermal annealing. Impressively, the SCLs show reversible RTP emission via alternant stimulation by UV light and heat. Photoactivated SCLs have phosphorescent efficiency of 8.50 % and a lifetime of 31.54 ms under ambient conditions. Regarding the dynamic RTP behavior and stretchability of SCLs, we demonstrate the applications in erasable data encryption and patterns on flexible substrates. This finding provides a design principle for obtaining SCLs with RTP and expands the potential applications of RTP materials in flexible optoelectronics.

10.
Nat Mater ; 20(11): 1539-1544, 2021 11.
Artigo em Inglês | MEDLINE | ID: mdl-34426660

RESUMO

High-efficiency blue phosphorescence emission is essential for organic optoelectronic applications. However, synthesizing heavy-atom-free organic systems having high triplet energy levels and suppressed non-radiative transitions-key requirements for efficient blue phosphorescence-has proved difficult. Here we demonstrate a simple chemical strategy for achieving high-performance blue phosphors, based on confining isolated chromophores in ionic crystals. Formation of high-density ionic bonds between the cations of ionic crystals and the carboxylic acid groups of the chromophores leads to a segregated molecular arrangement with negligible inter-chromophore interactions. We show that tunable phosphorescence from blue to deep blue with a maximum phosphorescence efficiency of 96.5% can be achieved by varying the charged chromophores and their counterions. Moreover, these phosphorescent materials enable rapid, high-throughput data encryption, fingerprint identification and afterglow display. This work will facilitate the design of high-efficiency blue organic phosphors and extend the domain of organic phosphorescence to new applications.


Assuntos
Conformação Molecular
11.
J Am Chem Soc ; 143(39): 16256-16263, 2021 Oct 06.
Artigo em Inglês | MEDLINE | ID: mdl-34550674

RESUMO

Ultralong organic phosphorescence (UOP) has aroused enormous interest in recent years. UOP materials are mainly limited to crystals or rigid host-guest systems. Their poor processability and mechanical properties critically hamper practical applications. Here, we reported a series of ultralong phosphorescent foams with high mechanical strength. Phosphorescence lifetime of the foam can reach up to 485.8 ms at room temperature. Impressively, lightweight gelatin foam can bear a compressive pressure of 4.44 MPa. Moreover, phosphorescence emission of polymer foam can be tuned from blue to orange through varying the excitation wavelength. Experimental data and theoretical calculations revealed that ultralong phosphorescence was ascribed to the fixation of multiple hydrogen bonds to the clusters of carbonyl groups. These results will allow for expanding the scope of luminescent foams, providing an ideal platform for developing ultralong phosphorescent materials with high mechanical strength.

12.
Anal Chem ; 93(44): 14643-14650, 2021 11 09.
Artigo em Inglês | MEDLINE | ID: mdl-34698497

RESUMO

Glycosylation is one of the most ubiquitous and complicated modifications of proteins and lipids. The revelation of glycosylation-mediated regulation mechanisms of biological processes relies critically on the tools that can reflect the spatial heterogeneity of cell surface glycans, for example, distinguishing glycans exhibited in lipid raft or nonraft domains. To achieve simultaneous visualization of raft and raft-harbored glycans on the cell surface, we combine specific raft recognition, glycan chemoselective labeling, and DNA dynamic hybridization techniques to develop a hierarchical fluorescence imaging strategy using N-acetyl-neuraminic acid (Sia) as the model sugar. We fabricate a raft probe and Sia probe for rafts and Sia, respectively. After specifically anchoring the two probes on the cell surface, the raft probe can be cyclically utilized to turn on the fluorescence of the Sia probe, only residing in rafts, via a proximity cascade DNA reaction. The duplex imaging capability for spatially relevant levels of biological structures enables the revelation of the reason for raft-confined Sia variation in different biological processes. Thus, this work provides an elegant and powerful tool for interrogation of the glycan regulation mechanisms on raft composition, organization, and functions and also contributes to the development of raft-carried glycoconjugate-based theranostic techniques.


Assuntos
Lipídeos , Microdomínios da Membrana , Membrana Celular , Imagem Óptica
13.
Anal Chem ; 93(16): 6516-6522, 2021 04 27.
Artigo em Inglês | MEDLINE | ID: mdl-33852275

RESUMO

Compared with short-lived emission probes featuring fluorescence imaging , the use of phosphorescent probes imparts the advantage of long-lived signal persistence that distinguishes against background fluorescence interference. However, the realization of ultralong organic phosphorescent (UOP) probes with an ultralong emission lifetime in an aqueous medium is still a challenge. Here, we present a rational strategy for obtaining UOP nanoparticles (NPs) in an air-saturated aqueous medium prepared using an organic phosphor (PDBCz) and a surfactant polymer (PVP), named PDBCz@PVP, showing an ultralong emission lifetime of 284.59 ms and a phosphorescence quantum efficiency of 7.6%. The excellent phosphorescence properties and water solubility of PDBCz@PVP make it a promising candidate for biological imaging. The as-prepared PDBCz@PVP NPs possess excellent luminescence intensity as well as illustrious biocompatibility both in vitro and in vivo. We demonstrate their use as an efficient phosphorescent nanoprobe both in living cells and zebrafish by capturing their afterglow emission signals under microscopy observation for the first time, realizing convenient and fast bioimaging with low cost, which allows for anti-fluorescence interference and shows promise for the future theragnostic applications in nanomedicine.


Assuntos
Medições Luminescentes , Nanopartículas , Peixe-Zebra , Animais , Luminescência , Polímeros
14.
Genomics ; 112(6): 4399-4405, 2020 11.
Artigo em Inglês | MEDLINE | ID: mdl-32738269

RESUMO

PURPOSE: Genetic polymorphisms act a crucial role in chronic obstructive pulmonary disease (COPD) progression. This study aimed to investigate the correlation between CYP3A4 variants and COPD risk. METHODS: We carried out a case-control study of 821 individuals (313 patients and 508 healthy subjects) to identify the correlation of CYP3A4 SNPs with COPD risk in the Hainan Han population. The association was evaluated by Odds ratios (OR) and 95% confidence intervals (CI). RESULTS: Our study showed that rs4646437 polymorphism was related to a significantly increased susceptibility to COPD (OR 1.45, 95% CI = 1.10-1.90, p = 0.008). Stratified analyses indicated that rs4646437 polymorphism was significantly related to an increased risk of COPD in males (OR 1.95, 95% CI = 1.19-3.20, p = 0.008). However, rs4646440 played a protective role in females (OR 0.54, 95% CI = 0.31-0.93, p = 0.024). Rs4646437 was found to significantly improve the risk of COPD in smokers (OR 1.67, 95% CI = 1.12-2.48, p = 0.011). While rs4646440 had a significantly lower susceptibility to COPD in non-smokers (OR 0.64, 95% CI = 0.45-0.90, p = 0.010). Haplotype analysis revealed that Ars4646440Trs35564277 haplotype of CYP3A4 was found to increase the risk of COPD in non-smokers (OR 1.71, 95% CI = 1.04-2.82, p = 0.034). CONCLUSION: Our result gives a new understanding of the association between CYP3A4 gene and COPD in the Hainan Han population.


Assuntos
Citocromo P-450 CYP3A/genética , Predisposição Genética para Doença , Polimorfismo de Nucleotídeo Único , Doença Pulmonar Obstrutiva Crônica/genética , Idoso , Idoso de 80 Anos ou mais , Estudos de Casos e Controles , China/etnologia , Feminino , Frequência do Gene , Haplótipos , Humanos , Masculino , Pessoa de Meia-Idade , Doença Pulmonar Obstrutiva Crônica/etnologia , Fumar
15.
Angew Chem Int Ed Engl ; 60(52): 27195-27200, 2021 Dec 20.
Artigo em Inglês | MEDLINE | ID: mdl-34532938

RESUMO

There are few reports about purely organic phosphorescence scintillators, and the relationship between molecular structures and radioluminescence in organic scintillators is still unclear. Here, we presented isomerism strategy to study the effect of molecular structures on radioluminescence. The isomers can achieve phosphorescence efficiency of up to 22.8 % by ultraviolet irradiation. Under X-ray irradiation, both m-BA and p-BA show excellent radioluminescence, while o-BA has almost no radioluminescence. Through experimental and theoretical investigation, we found that radioluminescence was not only affected by non-radiation in emissive process, but also highly depended on the material conductivity caused by the different molecular packing. This study not only allows us to clearly understand the relationship between the molecular structures and radioluminescence, but also provides a guidance to rationally design new organic scintillators.

16.
Small ; 16(8): e1906733, 2020 02.
Artigo em Inglês | MEDLINE | ID: mdl-32003926

RESUMO

Ultralong organic phosphorescence (UOP), enabling of persistent luminescence after removal of external excitation light, shows great promise in biological applications such as bioimaging in virtue of antibackground fluorescence interference. Despite of good biocompatibility and outstanding phosphorescent properties, most current organic phosphors are hydrophobic with poor water solubility in the form of bulk crystal with large size, limiting their potential in the biological field. Here, a facile and versatile approach is provided to obtain nanoscale hydrophilic phosphorescent phosphors (HPPs) by physically loading ultralong organic phosphors into hollow mesoporous silica nanoparticles. The as-prepared HPPs can be well suspended in aqueous solution and effectively internalized by HeLa cells with very low cytotoxicity. Such HPPs are successfully applied for afterglow bioimaging in living nude mice with a very high signal-to-noise ratio up to 31. The current study not only provides a universal strategy to realize UOP in aqueous media but also demonstrates their great potential for biomedical purposes as an advanced imaging indicator with long-lived emission lifetime.


Assuntos
Diagnóstico por Imagem , Nanopartículas , Dióxido de Silício , Animais , Diagnóstico por Imagem/métodos , Células HeLa , Humanos , Interações Hidrofóbicas e Hidrofílicas , Luminescência , Camundongos , Camundongos Nus , Nanopartículas/química , Nanopartículas/metabolismo , Dióxido de Silício/química
17.
Chemistry ; 26(20): 4437-4448, 2020 Apr 06.
Artigo em Inglês | MEDLINE | ID: mdl-31788882

RESUMO

Ultralong organic phosphorescence (UOP) of metal-free organic materials has received considerable attention recently owing to their long-lived emission lifetimes, and the fact that they present an attractive alternative to persistent luminescence in inorganic phosphors. Enormous research effort has been devoted on improving UOP performance in metal-free organic phosphors by promoting the intersystem crossing (ISC) process and suppressing the non-radiative decay of triplet state excitons. This minireview summarizes the recent advances in the rational approaches for manipulating the UOP properties of small molecular crystals, such as phosphorescence lifetime, efficiency, and emission colors. Finally, the present challenges and future development of this field are proposed. This review will provide a guideline to rationally design more advanced metal-free organic phosphorescence materials for potential applications.

18.
Mol Cell Probes ; 50: 101498, 2020 04.
Artigo em Inglês | MEDLINE | ID: mdl-31891749

RESUMO

In cancer patients, the prevalence of myeloid-derived suppressor cells (MDSCs) is correlated with the degree of malignancy. In the present study, we investigated the role of circulating M-MDSCs in premetastatic niche formation using a mouse syngeneic tumor model and found that there was an increased frequency of M-MDSCs in the peripheral blood of tumor-bearing mice. M-MDSCs tracking and lung tissue histological analyses revealed that the malignant conditions promote the residence of circulating M-MDSCs and increased tumor cell arrest in the lungs. We further found that MMP-9 expression was increased in the circulating M-MDSCs and the administration of an MMP-9 inhibitor suppressed M-MDSCs transplantation-induced tumor cell arrest in the lung. Therefore, our findings suggest that the expansion of circulating M-MDSCs during tumor progression contributes to premetastatic niche formation by increasing MMP-9 expression.


Assuntos
Neoplasias Pulmonares/enzimologia , Neoplasias Pulmonares/patologia , Pulmão/patologia , Metaloproteinase 9 da Matriz/metabolismo , Monócitos/patologia , Células Supressoras Mieloides/patologia , Sequência de Aminoácidos , Animais , Progressão da Doença , Feminino , Regulação Neoplásica da Expressão Gênica , Terapia de Imunossupressão , Neoplasias Pulmonares/sangue , Neoplasias Pulmonares/genética , Masculino , Metaloproteinase 9 da Matriz/química , Melanoma Experimental/patologia , Camundongos Endogâmicos C57BL , Metástase Neoplásica , Peptídeos/química
19.
Anal Bioanal Chem ; 411(30): 8103-8111, 2019 Dec.
Artigo em Inglês | MEDLINE | ID: mdl-31758198

RESUMO

A novel sensitive and selective probe for the important antibiotic vancomycin (Van) has been synthesized by integrating a coumarin and a fluorescein as dual fluorescence reporters and a Van binding peptide D-Ala-D-Ala. Only weak green fluorescence was initially observed, which was mostly attributed to fluorescence self-quenching induced by fluorophore stacking. Upon the binding of Van with the D-Ala-D-Ala peptide, the fluorescence turned on, probably due the disaggregation of fluorophores. The intensity ratio of the dual emission bands I519/I446 exhibited an excellent linear relationship with the concentration of Van increasing from 0-20 µM in synthetic urine. The lowest detection limit was calculated to be 92.8 nM in urine, which made the probe applicable in clinically relevant concentration ranges. The synthetic probe has also shown the potential for Van detection in human serum. More interestingly, this probe has been successfully applied for in vivo imaging of Van in zebrafish. Graphical Abstract.


Assuntos
Antibacterianos/análise , Corantes Fluorescentes/química , Vancomicina/análise , Antibacterianos/urina , Ensaio de Imunoadsorção Enzimática , Humanos , Limite de Detecção , Espectrometria de Fluorescência/métodos , Vancomicina/urina
20.
Angew Chem Int Ed Engl ; 58(20): 6645-6649, 2019 May 13.
Artigo em Inglês | MEDLINE | ID: mdl-30801896

RESUMO

Developing pure organic materials with ultralong lifetimes is attractive but challenging. Here we report a concise chemical approach to regulate the electronic configuration for phosphorescence enhancement. After the introduction of d-pπ bonds into a phenothiazine model system, a phosphorescence lifetime enhancement of up to 19 times was observed for DOPPMO, compared to the reference PPMO. A record phosphorescence lifetime of up to 876 ms was obtained in phosphorescent phenothiazine. Theoretical calculations and single-crystal analysis reveal that the d-pπ bond not only reduces the (n, π*) proportion of the T1 state, but also endows the rigid molecular environment with multiple intermolecular interactions, thus enabling long-lived phosphorescence. This finding makes a valuable contribution to the prolongation of phosphorescence lifetimes and the extension of the scope of phosphorescent materials.

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