Exosome nanovesicles: A potential carrier for therapeutic delivery DOI Creative Commons
Vivek P. Chavda, Anjali Pandya, Lalit Kumar

и другие.

Nano Today, Год журнала: 2023, Номер 49, С. 101771 - 101771

Опубликована: Фев. 7, 2023

Exosomes are small nanosized biovesicles that form when multivesicular bodies and the plasma membrane fuse released into surrounding body fluids. They best known for their multifunction in mediating intercellular communication by transferring various biomolecules, including DNA, RNAs, proteins, lipids, a short- long-distance manner have been identified as health disease messengers. Importantly, exosomes necessary physiological processes disease. The generation of depends on status disease, which usually exhibits opposite roles inducing enhanced cellular stress damage. Recently, exosome-based nanotechnologies provided unprecedented opportunities to boost developments exosome-related biology, chemistry, pathology, therapeutics different diseases based unique structural/compositional/morphological characteristics next-generation nanomedicines. Herein, we provide comprehensive overview recent advances exosome nanotechnology research, classification, isolation preparation, constitution, biological function, nanobiomedical applications treatment diagnosis. Furthermore, future prospects were also concluded. This review will more inspiration promoting development advanced theranostic nanoplatforms nanotechnology.

Язык: Английский

Exosomes: Large-scale production, isolation, drug loading efficiency, and biodistribution and uptake DOI
Ilgin Kimiz‐Gebologlu, Suphi Ş. Öncel

Journal of Controlled Release, Год журнала: 2022, Номер 347, С. 533 - 543

Опубликована: Май 24, 2022

Язык: Английский

Процитировано

397

Exosomes─Nature’s Lipid Nanoparticles, a Rising Star in Drug Delivery and Diagnostics DOI Creative Commons

Rumiana Tenchov,

Janet M. Sasso, Xinmei Wang

и другие.

ACS Nano, Год журнала: 2022, Номер 16(11), С. 17802 - 17846

Опубликована: Ноя. 10, 2022

Exosomes are a subgroup of nanosized extracellular vesicles enclosed by lipid bilayer membrane and secreted most eukaryotic cells. They represent route intercellular communication participate in wide variety physiological pathological processes. The biological roles exosomes rely on their bioactive cargos, including proteins, nucleic acids, lipids, which delivered to target Their distinctive properties─innate stability, low immunogenicity, biocompatibility, good biomembrane penetration capacity─allow them function as superior natural nanocarriers for efficient drug delivery. Another notably favorable clinical application is diagnostics. hold various biomolecules from host cells, indicative pathophysiological conditions; therefore, they considered vital biomarker discovery Here, we use data the CAS Content Collection provide landscape overview current state delineate trends research advancement exosome applications therapeutics diagnostics across time, geography, composition, cargo loading, development pipelines. We discuss composition pathway, biogenesis secretion cells recipient cell uptake. assess methods isolation purification, therapy diagnostics, pipelines, exploration goals companies, assortment diseases aim treat, stages research, publication trends. hope this review will be useful understanding knowledge field medical exosomes, an effort further solve remaining challenges fulfilling potential.

Язык: Английский

Процитировано

340

Extracellular vesicle-loaded hydrogels for tissue repair and regeneration DOI Creative Commons

Yikun Ju,

Yue Hu, Yang Pu

и другие.

Materials Today Bio, Год журнала: 2022, Номер 18, С. 100522 - 100522

Опубликована: Дек. 21, 2022

Extracellular vesicles (EVs) are a collective term for nanoscale or microscale secreted by cells that play important biological roles. Mesenchymal stem class of with the potential self-healing and multidirectional differentiation. In recent years, numerous studies have shown EVs, especially those mesenchymal cells, can promote repair regeneration various tissues and, thus, significant in regenerative medicine. However, due to rapid clearance capacity circulatory system, EVs barely able act persistently at specific sites target tissues. Hydrogels good biocompatibility loose porous structural properties allow them serve as EV carriers, thereby prolonging retention certain areas slowing release EVs. When needed function sites, EV-loaded hydrogels stand an excellent approach. this review, we first introduce sources, roles, extraction characterization methods describe their current application status. We then review different types discuss factors influencing abilities carry summarize several strategies loading into characterizing hydrogels. Furthermore, applications tissue repair. This article concludes summary state research on outlook future directions, which hope will provide promising ideas researchers.

Язык: Английский

Процитировано

282

Clinical applications of stem cell-derived exosomes DOI Creative Commons
Fei Tan, Xuran Li, Zhao Wang

и другие.

Signal Transduction and Targeted Therapy, Год журнала: 2024, Номер 9(1)

Опубликована: Янв. 12, 2024

Abstract Although stem cell-based therapy has demonstrated considerable potential to manage certain diseases more successfully than conventional surgery, it nevertheless comes with inescapable drawbacks that might limit its clinical translation. Compared cells, cell-derived exosomes possess numerous advantages, such as non-immunogenicity, non-infusion toxicity, easy access, effortless preservation, and freedom from tumorigenic ethical issues. Exosomes can inherit similar therapeutic effects their parental cells embryonic adult through vertical delivery of pluripotency or multipotency. After a thorough search meticulous dissection relevant literature the last five years, we present this comprehensive, up-to-date, specialty-specific disease-oriented review highlight surgical application exosomes. derived (e.g., embryonic, induced pluripotent, hematopoietic, mesenchymal, neural, endothelial cells) are capable treating encountered in orthopedic neurosurgery, plastic general cardiothoracic urology, head neck ophthalmology, obstetrics gynecology. The diverse cells-derived hierarchical translation tissue-specific responses, cell-specific molecular signaling pathways. In review, viable potent alternative managing various conditions. We recommend future research combines wisdoms surgeons, nanomedicine practitioners, cell researchers intriguing area.

Язык: Английский

Процитировано

240

Role of exosomal non-coding RNAs from tumor cells and tumor-associated macrophages in the tumor microenvironment DOI Creative Commons

Zijie Xu,

Yi Chen, Ling Ma

и другие.

Molecular Therapy, Год журнала: 2022, Номер 30(10), С. 3133 - 3154

Опубликована: Апрель 9, 2022

Exosomes have a crucial role in intercellular communication and mediate interactions between tumor cells tumor-associated macrophages (TAMs). Exosome-encapsulated non-coding RNAs (ncRNAs) are involved various physiological processes. Tumor-derived exosomal ncRNAs induce M2 macrophage polarization through signaling pathway activation, signal transduction, transcriptional post-transcriptional regulation. Conversely, TAM-derived promote proliferation, metastasis, angiogenesis, chemoresistance, immunosuppression. MicroRNAs gene silencing by directly targeting mRNAs, whereas lncRNAs circRNAs act as miRNA sponges to indirectly regulate protein expressions. The of tumor-host is ubiquitous. Current research increasingly focused on the microenvironment. On basis "cancer-immunity cycle" hypothesis, we discuss effects immune T cell exhaustion, overexpression programmed death ligands, create immunosuppressive Furthermore, potential applications prospects clinical biomarkers drug delivery systems. Non-coding do not encode proteins but control expression function.1Hombach S. Kretz M. RNAs: classification, biology functioning.Adv. Exp. Med. Biol. 2016; 937: 3-17Crossref PubMed Scopus (346) Google Scholar, 2Chan J.J. Tay Y. Noncoding RNA:RNA regulatory networks cancer.Int. J. Mol. Sci. 2018; 19: 1310Crossref (608) 3Guil Esteller RNA-RNA regulation: coding noncoding players.Trends Biochem. 2015; 40: 248-256Abstract Full Text PDF Scholar Several types ncRNAs, including microRNAs (miRNAs), long (lncRNAs), circular (circRNAs), affect growth, metabolism multiple mechanisms.3Guil 4Anastasiadou E. Jacob L.S. Slack F.J. RNA cancer.Nat. Rev. Cancer. 18: 5-18Crossref (900) 5Goodall G.J. Wickramasinghe V.O. 2021; 21: 22-36Crossref (337) miRNAs 20–25 nucleotide that at level binding 3′ untranslated region (3′ UTR) target thus regulating other cellular processes.6Ha Kim V.N. Regulation microRNA biogenesis.Nat. Cell 2014; 15: 509-524Crossref (3372) Scholar,7Dong H. Lei Ding L. Wen Ju Zhang X. MicroRNA: function, detection, bioanalysis.Chem. 2013; 113: 6207-6233Crossref (823) longer than 200 nucleotides regulation nucleus cytoplasm.8Chen L.L. Linking localization function.Trends 41: 761-772Abstract (592) Scholar,9Quinn Chang H.Y. Unique features biogenesis function.Nat. Genet. 17: 47-62Crossref (2150) modulate stability, translation, translocation mRNAs.9Quinn Scholar,10Statello Guo C.J. Chen Huarte Gene its biological functions.Nat. 22: 96-118Crossref (817) increase mRNA expressions sponging competitive endogenous (ceRNAs), secreted either alone or bound proteins.11Tay Rinn Pandolfi P.P. multilayered complexity ceRNA crosstalk competition.Nature. 505: 344-352Crossref (2450) Scholar,12Lin C. Yang Long cancer: wiring circuitry.Trends 28: 287-301Abstract (330) characterized covalently closed-loop structure without 5′ cap poly(A) tail.13Yu C.Y. Kuo H.C. emerging roles functions their generation.J. Biomed. 2019; 26: 29Crossref (167) Scholar,14Kristensen Andersen M.S. Stagsted L.V.W. Ebbesen K.K. Hansen T.B. Kjems biogenesis, characterization RNAs.Nat. 20: 675-691Crossref (1539) These implicated spongings, interactions, nuclear transcription pre-mRNA splicing.15Wang R. Li N. Jia Pan Liang CircNT5E acts sponge miR-422a glioblastoma tumorigenesis.Cancer Res. 78: 4812-4825Crossref (199) Scholar,16Qian Yu Z. Meng Huang Wang P. significance human cancers.Biochim. Biophys. Acta 1870: 247-260Crossref (0) 40–150 nm extracellular vesicles pathological processes mediating communication.17Hessvik N.P. Llorente A. knowledge exosome release.Cell Life 75: 193-208Crossref (1112) Scholar,18Pegtel D.M. Gould S.J. Exosomes.Annu. 88: 487-514Crossref (793) content exosomes released donor protected from enzymatic hydrolysis.19Abels E.R. Breakefield X.O. Introduction vesicles: cargo selection, content, release, uptake.Cell. Neurobiol. 36: 301-312Crossref (713) 20Mathieu Martin-Jaular Lavieu G. Théry Specificities secretion uptake for cell-to-cell communication.Nat. 9-17Crossref (1420) 21Mashouri Yousefi Aref A.R. Ahadi A.M. Molaei F. Alahari S.K. Exosomes: composition, mechanisms cancer metastasis resistance.Mol. 75Crossref (410) fundamental resistance.21Mashouri 22van Niel D'Angelo Raposo Shedding light vesicles.Nat. 213-228Crossref (2898) 23Zhang D. development, immunity.Biochim. 1871: 455-468Crossref (215) Tumoral secrete microenvironment (TIME).23Zhang Scholar,24Kalluri function cancer.J. Clin. Invest. 126: 1208-1215Crossref (967) (TEXs) immunological activities, polarization, regulation, inhibition natural killer (NK) activity.25Whiteside T.L. progression.Adv. Chem. 74: 103-141Crossref (402) 26Kok V.C. C.C. Cancer-derived exosomes: biomarker development.Int. Nanomed. 2020; 8019-8036Crossref (50) 27Greening D.W. Gopal Xu Simpson R.J. W. cancer.Semin. Dev. 72-81Crossref (401) TEXs also malignancy, suggesting key tumoral cells.28Xie Zhou Fang Su Tu Extracellular immunotherapy.Adv. 6: 1901779Crossref (103) 29Veerman R.E. Güçlüler Akpinar Eldh Gabrielsson Immune cell-derived - therapeutic applications.Trends 25: 382-394Abstract (110) 30Yan Jiang cancer-immunity cycle.Trends 506-517Abstract (46) development immunosuppression attracted increasing attention.31Sun Shi K. Liu Q. Song Yuan Effect applications.Mol. 147Crossref 32Cheng Zhu Peng Exosomal Glioma: 66Crossref (131) 33Xie Dang Yue Zhai Yan Lu cancer.Mol. 37Crossref (134) can be used because high encapsulation efficiency ability transport anti-cancer drugs, agents, nucleic acids, gene-editing systems such CRISPR-Cas9.34Pullan J.E. Confeld M.I. Osborn J.K. Sarkar Mallik carriers therapy.Mol. Pharm. 16: 1789-1798Crossref (76) 35Liu Cheng Delivery strategies CRISPR-Cas9 system applications.J. Control. Release. 2017; 266: 17-26Crossref (257) 36Ghaemi Bagheri Abnous Taghdisi S.M. Ramezani Alibolandi CRISPR-cas9 genome editing targeted therapy.Life 267: 118969Crossref (7) Macrophages phagocytic cells, phenotypes influenced cytokines factors TIME.37Belgiovine D'Incalci Allavena Frapolli Tumor-associated anti-tumor therapies: complex links.Cell. 73: 2411-2424Crossref assume classically activated pro-inflammatory (M1) phenotype an alternatively anti-inflammatory (M2) phenotype.38Orecchioni Ghosheh Pramod A.B. Ley Macrophage polarization: different signatures M1(LPS+) vs. Classically M2(LPS-) Alternatively macrophages.Front. Immunol. 10: 1084Crossref (541) (TAMs) M1 early stages cancer.37Belgiovine In later stage, growth mediators, IL-4, IL-10, TGF-β, expressed TIME, inducing polarization.37Belgiovine M1-M2 highly dynamic reversible. TAMs produce inhibit activity TIME.39Yin Han Zheng B. Zhao SALL4-mediated upregulation miR-146a-5p drives T-cell exhaustion HCC.Oncoimmunology. 8: 1601479Crossref (3) TAM infiltration solid tumors underscores these progression immunosuppression.39Yin 40Ruffell Coussens L.M. resistance cancer.Cancer Cell. 27: 462-472Abstract (800) 41Sica Erreni Porta pathology.Cell. 72: 4111-4126Crossref (352) divided into M2a, M2b, M2c, M2d.42Rőszer T. Understanding mysterious activation markers effector mechanisms.Mediators Inflamm. 2015: 816460Crossref M2a subgroup IL-4 IL-13 produces CD163, CD206, IL1Ra.42Rőszer M2b stimulated complexes bacterial lipopolysaccharide CD86, IL-6, TNF-α.42Rőszer M2c induced glucocorticoids, TGF-β TGF-β; addition, this active against apoptotic cells.42Rőszer M2d subgroup, IL-6 adenosine, secretes (high levels IL-10 low IL-12) vascular endothelial factor (VEGF) angiogenesis.42Rőszer Some pathways switch.41Sica Scholar,43Shapouri-Moghaddam Mohammadian Vazini Taghadosi Esmaeili S.A. Mardani Seifi Mohammadi Afshari J.T. Sahebkar plasticity, health disease.J. Physiol. 233: 6425-6440Crossref (1441) Pro-inflammatory malignant behavior, promotes tumorigenesis evasion.41Sica Therefore, fine-tuned TIME. Tumor tissues may contain mixed populations with spectrum states. However, review, assumed phenotype, described literature.37Belgiovine Increased attention has been given TAMs. polarized support forming cycle which (Figure 1). This review discusses during initiation controlled influence formation TIME based model, application diagnostic prognostic targets. involves networks.38Orecchioni phosphatidylinositol 3-kinase (PI3K)/AKT JAK/STAT factors, transducer activator (STAT) family, peroxisome proliferator-activated receptor-γ (PPARγ), interferon polarization.44Czimmerer Daniel Horvath Rückerl Nagy Kiss Peloquin Budai M.M. Cuaranta-Monroy I. Simandi et al.The STAT6 mediates direct repression inflammatory enhancers limits macrophages.Immunity. 48: 75-90.e76Abstract (112) Scholar,45Vergadi Ieronymaki Lyroni Vaporidi Tsatsanis Akt M1/M2 polarization.J. 198: 1006-1014Crossref (398) Tumors controlling factors. For instance, HPV+ head neck squamous carcinoma (HNSCC), miR-9 was enriched transported macrophages, downregulating PPARδ.46Tong Mao Xie Sun Wei HPV + HNSCC-derived induces increases radiosensitivity.Cancer Lett. 478: 34-44Crossref (23) miR-451/miR-21 were detected primary multiforme (GBM) taken up brain mice, decreasing c-Myc levels. miR-21 miR-451 increased microglia co-cultured GBM heparin reduced effect.47van der Vos K.E. Abels Lai Carrizosa Oakley Prabhakar Mardini O. Crommentuijn M.H. Skog al.Directly visualized glioblastoma-derived transfer microglia/macrophages brain.Neuro Oncol. 58-69Crossref (207) prostate (PCa), let-7a-5p let7-b, -g, -i downregulated integrin-β3, causing PCa migration.48Ferguson Lee Deci Nguyen phenotypic distinct sources: comparative study composition.AAPS 67Crossref lncRNA TUC339 hepatocellular (HCC) promoted leading cytokine production, compromised phagocytosis, decreased co-stimulatory molecule macrophages.49Kogure I.K. Lin W.L. Patel vesicle-mediated novel TUC339: mechanism cancer.Genes 4: 261-272Crossref (239) Scholar,50Li Wu HCC-derived TUC339.Int. 2958Crossref (36) receptor CXCR chemokine pathways, explain underlying regulation.50Li miR-21-5p colorectal (CRC) cells.51Shao Shen al.Colorectal cancer-derived small establish premetastatic niche liver metastasis.Carcinogenesis. 39: 1368-1379Crossref (6) CRC lines SW480, SW620, LoVo injected nude mice significantly macrophages. via TLR7 pre-metastatic survival colonization, ultimately metastasis.51Shao metabolic enzymes. melanoma miR-125b-5p lysosomal acid lipase A switching survival.52Gerloff Lützkendorf Moritz R.K.C. Wersig Mäder Müller L.P. Sunderkötter Melanoma-derived educates associated (LIPA).Cancers. 12: 464Crossref BMP-7, PI3K/AKT pathway.45Vergadi Scholar,53Covarrubias A.J. Aksoylar H.I. Horng Control mTOR signaling.Semin. 286-296Crossref (189) Scholar,54Zhao Kong F.Q. Jie A.D. Y.Q. D.D. Z.Q. al.Macrophage MSR1 BMSC osteogenic differentiation M2-like activating PI3K/AKT/GSK3β/β-catenin pathway.Theranostics. 17-35Crossref (37) Phosphatase tension homolog deleted chromosome ten (PTEN) inhibits AKT dephosphorylating PIP3.45Vergadi Scholar,55Lu PTEN/PI3k/AKT regulates emphysematous mice.Scand. 85: 395-405Crossref (38) bladder regulated inhibiting PTEN enhanced STAT3 expression, promoting migration invasion.56Lin Yin H.B. X.Y. G.M. He W.Y. Gou Bladder cell-secreted activates progression.Int. 56: 151-164PubMed miR-130b-3p, miR-425-5p, miR-25-3p pathway. epithelial-mesenchymal transition (EMT) VEGF metastasis.57Wang Si Cui Qu contribute CXCL12/CXCR4-induced enhancing macrophages.Cancer 474: 36-52Crossref (108) Scholar,58Wang Corrigendum "Exosome-encapsulated macrophages" [Canc. 474 (2020) 36-52].Cancer 2022; 525: 200-202Crossref circFARSA upregulated non-small lung (NSCLC) exosomes.59Chen PTEN/PI3K/AKT metastasis.Cancer Treat. Commun. 100412Crossref (11) ubiquitination degradation PTEN, polarization.59Chen RNA-binding eIF4A3 triggered cyclization EMT NSCLC cells.59Chen STAT1/5 STAT 3/6 respectively.60Zhao Bian Y.Y. Y.J. Ma Y.T. Pei Zeng HuoXueTongFu formula alleviates intraperitoneal adhesion SOCS/JAK2/STAT/PPAR-γ signalling pathway.Mediators 2019: 1769374Crossref (14) Scholar,61Hu Ivashkiv L.B. Crosstalk among Jak-STAT, Toll-like receptor, ITAM-dependent activation.J. Leukoc. 2007; 82: 237-243Crossref (157) members suppressor (SOCS) family.60Zhao miR-29a-3p oral SOCS1/STAT6 signaling.62Cai Qiao Gao Oral carcinoma-derived subtype mediated exosome-enclosed miR-29a-3p.Am. 316: C731-C740Crossref co-culture system, miR-223 cervical (CSCC) CSCC creating positive feedback loop.63Zhang Qian STAT3-miR-223-TGFBR3/HMGCS1 axis modulates carcinoma.Mol. 14: 2313-2331Crossref Moreover, repressed TGFBR3 HMGCS1 UTRs, resulting anchorage-independent growth.63Zhang Hypoxia stimulates secretion, hypoxic trigger HIF1α- HIF2α-dependent manner.64Escribese Casas Corbí A.L. Influence oxygen tensions polarization.Immunobiology. 2012; 217: 1233-1240Crossref Scholar,65Díaz-Bulnes Saiz M.L. López-Larrea Rodríguez R.M. hypoxia ER stress res

Язык: Английский

Процитировано

209

Recent advances in exosome-mediated nucleic acid delivery for cancer therapy DOI Creative Commons
Ying Zhang, Qiqi Liu, Xinmeng Zhang

и другие.

Journal of Nanobiotechnology, Год журнала: 2022, Номер 20(1)

Опубликована: Июнь 14, 2022

Abstract Cancer is a leading public health problem worldwide. Its treatment remains daunting challenge, although significant progress has been made in existing treatments recent years. A large concern the poor therapeutic effect due to lack of specificity and low bioavailability. Gene therapy recently emerged as powerful tool for cancer therapy. However, delivery methods limit its effects. Exosomes, subset extracellular vesicles secreted by most cells, have characteristics good biocompatibility, toxicity immunogenicity, great designability. In past decades, carriers diagnostic markers, they caught extensive attention. This review introduced exosomes, focused on their applications DNA, messenger RNA (mRNA), microRNA (miRNA), small interfering (siRNA), circular (circRNA) other nucleic acids. Meanwhile, application exosome-based clinical trials were presented discussed. Through systematic summarization analysis, advances current challenges exosome-mediated acid are introduced, which will provide theoretical basis development drugs. Graphical

Язык: Английский

Процитировано

199

Exosome engineering in cell therapy and drug delivery DOI Open Access
Somayeh Sadeghi, Fahimeh Ramezani Tehrani, Safa Tahmasebi

и другие.

Inflammopharmacology, Год журнала: 2023, Номер 31(1), С. 145 - 169

Опубликована: Янв. 7, 2023

Язык: Английский

Процитировано

177

M2-type exosomes nanoparticles for rheumatoid arthritis therapy via macrophage re-polarization DOI
Hui Li, Yue Feng, Xiu Zheng

и другие.

Journal of Controlled Release, Год журнала: 2021, Номер 341, С. 16 - 30

Опубликована: Ноя. 15, 2021

Язык: Английский

Процитировано

172

Macrophage-tumor chimeric exosomes accumulate in lymph node and tumor to activate the immune response and the tumor microenvironment DOI
Shuang Wang, Feng Li, Tong Ye

и другие.

Science Translational Medicine, Год журнала: 2021, Номер 13(615)

Опубликована: Окт. 13, 2021

Despite multiple immunotherapeutic technologies that achieve potent T cell activation, effector cells still lack efficiency because of the highly immunosuppressive conditions in tumor microenvironment. Inspired by recent advances nano-sized secreted vesicles known as exosomes therapeutic agents and research revealing circulating cancer have a “homing” capacity to return main sites, we generated macrophage-tumor hybrid cells. We introduced nuclei isolated from into activated M1-like macrophages produce chimeric (aMT-exos). The aMT-exos were able accumulate both lymph nodes diverse tumors xenograft mice. They entered primed activation classical antigen-presenting cell–induced immunostimulatory manner unique “direct exosome interaction” manner. also had strong “homing behavior” where they ameliorated immunosuppression. effective inducing regression extending survival primary mouse models lymphoma breast melanoma cancers. In addition, when combined with anti–programmed death 1 (a-PD1) treatment, extend metastatic postsurgical recurrence models. Such coactivation immune response microenvironment enabled confer efficient inhibition tumors, metastases, postoperative for personalized immunotherapy, which warrants further exploration clinical setting.

Язык: Английский

Процитировано

167

Exosomes as Naturally Occurring Vehicles for Delivery of Biopharmaceuticals: Insights from Drug Delivery to Clinical Perspectives DOI Creative Commons
Arun Butreddy, Nagavendra Kommineni,

Narendar Dudhipala

и другие.

Nanomaterials, Год журнала: 2021, Номер 11(6), С. 1481 - 1481

Опубликована: Июнь 3, 2021

Exosomes as nanosized vesicles are emerging drug delivery systems for therapeutics owing to their natural origin, ability mediate intercellular communication, and potential encapsulate various biological molecules such proteins nucleic acids within the lipid bilayer membrane or in lumen. contain endogenous components (proteins, lipids, RNA) that could be used deliver cargoes target cells, offering an opportunity diagnose treat diseases. Owing travel safely extracellular fluid transport cells with high efficacy, exosomes offer enhanced of vivo. However, several challenges related stabilization exosomes, production sufficient amounts safety efficient loading drugs into clearance from circulation, transition bench scale clinical may limit development use. For use it is important understand molecular mechanisms behind function exosome vesicles. This review exploits techniques isolation characterization enhance therapeutic outcome methods. Further, routes administration, trials, regulatory aspects will discussed this review.

Язык: Английский

Процитировано

152