Ma L, Li Y, Peng J, Wu D, Zhao X, Cui Y, et al. Discovery of the migrasome, an organelle mediating launch of cytoplasmic contents throughout cell migration. Cell Res. 2015;25(1):24–38.
Jiang D, Jiang Z, Lu D, Wang X, Liang H, Zhang J, et al. Migrasomes present regional cues for organ morphogenesis throughout zebrafish gastrulation. Nat Cell Biol. 2019;21(8):966–77.
Zhang C, Li T, Yin S, Gao M, He H, Li Y, et al. Monocytes deposit migrasomes to advertise embryonic angiogenesis. Nat Cell Biol. 2022;24(12):1726–38.
Jiao H, Jiang D, Hu X, Du W, Ji L, Yang Y, et al. Mitocytosis, a migrasome-mediated mitochondrial quality-control course of. Cell. 2021;184(11):2896–910.
Zhu M, Zou Q, Huang R, Li Y, Xing X, Fang J, et al. Lateral switch of mRNA and protein by migrasomes modifies the recipient cells. Cell Res. 2021;31(2):237–40.
Jiao H, Li X, Li Y, Guo Y, Hu X, Sho T, et al. Localized, extremely environment friendly secretion of signaling proteins by migrasomes. Cell Res. 2024;34(8):572–85.
Turei D, Valdeolivas A, Gul L, Palacio-Escat N, Klein M, Ivanova O, et al. Built-in intra- and intercellular signaling data for multicellular omics evaluation. Mol Syst Biol. 2021;17(3): e9923.
Szklarczyk D, Gable AL, Lyon D, Junge A, Wyder S, Huerta-Cepas J, et al. STRING v11: protein–protein affiliation networks with elevated protection, supporting purposeful discovery in genome-wide experimental datasets. Nucleic Acids Res. 2019;47(D1):D607–13.
Tkach M, Thery C. Communication by extracellular vesicles: the place we’re and the place we have to go. Cell. 2016;164(6):1226–32.
Andaloussi ELS, Mager I, Breakefield XO, Wooden MJA. Extracellular vesicles: biology and rising therapeutic alternatives. Nat Rev Drug Discov. 2013;12(5):347–57.
Jiang Y, Liu X, Ye J, Ma Y, Mao J, Feng D, et al. Migrasomes, a brand new mode of intercellular communication. Cell Commun Sign. 2023;21(1):105.
Zhang Okay, Zhu Z, Jia R, Wang NA, Shi M, Wang Y, et al. CD151-enriched migrasomes mediate hepatocellular carcinoma invasion by conditioning most cancers cells and selling angiogenesis. J Exp Clin Most cancers Res. 2024;43(1):160.
Zhang R, Peng J, Zhang Y, Zheng Okay, Chen Y, Liu L, et al. Pancreatic most cancers cell-derived migrasomes promote most cancers development by fostering an immunosuppressive tumor microenvironment. Most cancers Lett. 2024;605: 217289.
Huang Z, Wang M, Chen Y, Tang H, Tang Okay, Zhao M, et al. Glioblastoma-derived migrasomes promote migration and invasion by releasing PAK4 and LAMA4. Commun Biol. 2025;8(1):91.
Zhang N, Gao S, Zhang L. Chikungunya virus nsP1 induces migrasome formation. J Infect. 2022;85(5):e158–61.
Lv L, Zhang L. Identification of poxvirus inside migrasomes suggests a novel mode of mpox virus unfold. J Infect. 2023;87(2):160–2.
Xu T, Li D, Luan J, Zhang L. Dasabuvir: an FDA-approved drug inhibiting poxvirus transmission by focusing on each migrasome formation and extracellular enveloped virus manufacturing. J Infect. 2025;90(2): 106403.
Solar P, Li Y, Yu W, Chen J, Wan P, Wang Z, et al. Low-intensity pulsed ultrasound improves myocardial ischaemia–reperfusion damage by way of migrasome-mediated mitocytosis. Clin Transl Med. 2024;14(7): e1749.
Hu M, Li T, Ma X, Liu S, Li C, Huang Z, et al. Macrophage lineage cells-derived migrasomes activate complement-dependent blood-brain barrier harm in cerebral amyloid angiopathy mouse mannequin. Nat Commun. 2023;14(1):3945.
Wu L, Yang S, Li H, Zhang Y, Feng L, Zhang C, et al. TSPAN4-positive migrasome derived from retinal pigmented epithelium cells contributes to the event of proliferative vitreoretinopathy. J Nanobiotechnol. 2022;20(1):519.
Wan S, Wang X, Chen W, Xu Z, Zhao J, Huang W, et al. Polystyrene nanoplastics activate autophagy and suppress trophoblast cell migration/invasion and migrasome formation to induce miscarriage. ACS Nano. 2024;18(4):3733–51.
Liu Y, Li S, Rong W, Zeng C, Zhu X, Chen Q, et al. Podocyte-released migrasomes in urine function an indicator for early podocyte damage. Kidney Dis (Basel). 2020;6(6):422–33.
Chen Y, Li Y, Li B, Hu D, Dong Z, Lu F. Migrasomes from adipose derived stem cells enrich CXCL12 to recruit stem cells by way of CXCR4/RhoA for a constructive suggestions loop mediating gentle tissue regeneration. J Nanobiotechnol. 2024;22(1):219.
Taylor AC, Robbins E. Observations on microextensions from the floor of remoted vertebrate cells. Dev Biol. 1963;6:660–73.
Lee SY, Choi SH, Kim Y, Ahn HS, Ko YG, Kim Okay, et al. Migrasomal autophagosomes relieve endoplasmic reticulum stress in glioblastoma cells. BMC Biol. 2024;22(1):23.
Huang Y, Zucker B, Zhang S, Elias S, Zhu Y, Chen H, et al. Migrasome formation is mediated by meeting of micron-scale tetraspanin macrodomains. Nat Cell Biol. 2019;21(8):991–1002.
Zhou Z, Yang Z, Zhou L, Yang M, He S. The versatile roles of testrapanins in most cancers from intracellular signaling to cell-cell communication: cell membrane proteins with out ligands. Cell Biosci. 2023;13(1):59.
Wu D, Xu Y, Ding T, Zu Y, Yang C, Yu L. Pairing of integrins with ECM proteins determines migrasome formation. Cell Res. 2017;27(11):1397–400.
Hemler ME. Focusing on of tetraspanin proteins–potential advantages and methods. Nat Rev Drug Discov. 2008;7(9):747–58.
Rubinstein E. The complexity of tetraspanins. Biochem Soc Trans. 2011;39(2):501–5.
Zhao X, Lei Y, Zheng J, Peng J, Li Y, Yu L, et al. Identification of markers for migrasome detection. Cell Discov. 2019;5:27.
Liang H, Ma X, Zhang Y, Liu Y, Liu N, Zhang W, et al. The formation of migrasomes is initiated by the meeting of sphingomyelin synthase 2 foci at the forefront of migrating cells. Nat Cell Biol. 2023;25(8):1173–84.
Ding T, Ji J, Zhang W, Liu Y, Liu B, Han Y, et al. The phosphatidylinositol (4,5)-bisphosphate-Rab35 axis regulates migrasome formation. Cell Res. 2023;33(8):617–27.
Dharan R, Huang Y, Cheppali SK, Goren S, Shendrik P, Wang W, et al. Tetraspanin 4 stabilizes membrane swellings and facilitates their maturation into migrasomes. Nat Commun. 2023;14(1):1037.
Li Y, Wen Y, Li Y, Tan X, Gao S, Fan P, et al. Rab10-CAV1 mediated intraluminal vesicle transport to migrasomes. Proc Natl Acad Sci USA. 2024;121(30): e1975700175.
Apte RS, Chen DS, Ferrara N. VEGF in signaling and illness: past discovery and growth. Cell. 2019;176(6):1248–64.
Ballmer-Hofer Okay. Vascular endothelial progress issue, from fundamental analysis to scientific purposes. Int J Mol Sci. 2018;19(12):3750.
Ribatti D. The invention of the elemental position of VEGF within the growth of the vascular system. Mech Dev. 2019;160: 103579.
Majesky MW. Vascular growth. Arterioscler Thromb Vasc Biol. 2018;38(3):e17-24.
Chung AS, Ferrara N. Developmental and pathological angiogenesis. Annu Rev Cell Dev Biol. 2011;27:563–84.
Qian BZ, Pollard JW. Macrophage range enhances tumor development and metastasis. Cell. 2010;141(1):39–51.
Borikun T, Mushii O, Pavlova A, Burda T, Zadvornyi T. Tumor microenvironment-associated miR-7-5p, miR-19a-3p, and miR-23b-3p expression in prostate most cancers with totally different development danger. Exp Oncol. 2024;45(4):432–42.
Peng Okay, Bai Y, Zhu Q, Hu B, Xu Y. Focusing on VEGF-neuropilin interactions: a promising antitumor technique. Drug Discov Immediately. 2019;24(2):656–64.
Melentijevic I, Toth ML, Arnold ML, Guasp RJ, Harinath G, Nguyen KC, et al. C. elegans neurons jettison protein aggregates and mitochondria beneath neurotoxic stress. Nature. 2017;542(7641):367–71.
Hayakawa Okay, Esposito E, Wang X, Terasaki Y, Liu Y, Xing C, et al. Switch of mitochondria from astrocytes to neurons after stroke. Nature. 2016;535(7613):551–5.
Torralba D, Baixauli F, Sanchez-Madrid F. Mitochondria know no boundaries: mechanisms and capabilities of intercellular mitochondrial switch. Entrance Cell Dev Biol. 2016;4:107.
Wang H, Ye J, Peng Y, Ma W, Chen H, Solar H, et al. CKLF induces microglial activation by way of triggering faulty mitophagy and mitochondrial dysfunction. Autophagy. 2024;20(3):590–613.
Solar Y, Cao Y, Wan H, Memetimin A, Cao Y, Li L, et al. A mitophagy sensor PPTC7 controls BNIP3 and NIX degradation to manage mitochondrial mass. Mol Cell. 2024;84(2):327–44.
Versteeg HH, Heemskerk JW, Levi M, Reitsma PH. New fundamentals in hemostasis. Physiol Rev. 2013;93(1):327–58.
Davie EW, Ratnoff OD. Waterfall sequence for intrinsic blood clotting. Science. 1964;145(3638):1310–2.
Macfarlane RG. An enzyme cascade within the blood clotting mechanism, and its operate as a biochemical amplifier. Nature. 1964;202:498–9.
Jiang D, Jiao L, Li Q, Xie R, Jia H, Wang S, et al. Neutrophil-derived migrasomes are a necessary a part of the coagulation system. Nat Cell Biol. 2024;26(7):1110–23.
Qin Y, Yang J, Liang C, Liu J, Deng Z, Yan B, et al. Pan-cancer evaluation identifies migrasome-related genes as a possible immunotherapeutic goal: a bulk omics analysis and single cell sequencing validation. Entrance Immunol. 2022;13: 994828.
Mattiola I, Mantovani A, Locati M. The tetraspan MS4A household in homeostasis, immunity, and illness. Traits Immunol. 2021;42(9):764–81.
Mattiola I, Tomay F, De Pizzol M, Silva-Gomes R, Savino B, Gulic T, et al. The macrophage tetraspan MS4A4A enhances dectin-1-dependent NK cell-mediated resistance to metastasis. Nat Immunol. 2019;20(8):1012–22.
Zhang H, Cao Okay, Xiang J, Zhang M, Zhu M, Xi Q. Hypoxia induces immunosuppression, metastasis and drug resistance in pancreatic cancers. Most cancers Lett. 2023;571: 216345.
Gu C, Chen P, Tian H, Yang Y, Huang Z, Yan H, et al. Focusing on preliminary tumour-osteoclast spatiotemporal interplay to stop bone metastasis. Nat Nanotechnol. 2024;19(7):1044–54.
Huang Z, Zhou L, Chen Z, Good EC, Huang C. Stress administration by autophagy: implications for chemoresistance. Int J Most cancers. 2016;139(1):23–32.
Knizhnik AV, Roos WP, Nikolova T, Quiros S, Tomaszowski KH, Christmann M, et al. Survival and loss of life methods in glioma cells: autophagy, senescence and apoptosis triggered by a single kind of temozolomide-induced DNA harm. PLoS ONE. 2013;8(1): e55665.
Li J, Burgess DJ. Nanomedicine-based drug supply in the direction of tumor organic and immunological microenvironment. Acta Pharm Sin B. 2020;10(11):2110–24.
Dai Q, Bertleff-Zieschang N, Braunger JA, Bjornmalm M, Cortez-Jugo C, Caruso F. Particle focusing on in complicated organic media. Adv Healthc Mater. 2018;7(1).
Chen E, Han S, Music B, Xu L, Yuan H, Liang M, et al. Mechanism investigation of hyaluronidase-combined multistage nanoparticles for stable tumor penetration and antitumor impact. Int J Nanomed. 2020;15:6311–24.
Chen Z, Pan H, Luo Y, Yin T, Zhang B, Liao J, et al. Nanoengineered CAR-T biohybrids for stable tumor immunotherapy with microenvironment photothermal-remodeling technique. Small. 2021;17(14): e2007494.
Waknine-Grinberg JH, Even-Chen S, Avichzer J, Turjeman Okay, Bentura-Marciano A, Haynes RK, et al. Glucocorticosteroids in nano-sterically stabilized liposomes are efficacious for elimination of the acute signs of experimental cerebral malaria. PLoS ONE. 2013;8(8): e72722.
Henrich-Noack P, Nikitovic D, Neagu M, Docea AO, Engin AB, Gelperina S, et al. The blood–mind barrier and past: nano-based neuropharmacology and the position of extracellular matrix. Nanomedicine-UK. 2019;17:359–79.
Cheng Y, Ren J, Fan S, Wu P, Cong W, Lin Y, et al. Nanoparticulates cut back tumor cell migration by affinity interactions with extracellular migrasomes and retraction fibers. Nanoscale Horiz. 2022;7(7):779–89.
Sattentau Q. Avoiding the void: cell-to-cell unfold of human viruses. Nat Rev Microbiol. 2008;6(11):815–26.
Liu Y, Zhu Z, Li Y, Yang M, Hu Q. Migrasomes launched by HSV-2-infected cells function a conveyance for virus unfold. Virol Sin. 2023;38(4):643–5.
Zhao W, Tang X, Zhang L. Virus-containing migrasomes allow poxviruses to evade tecovirimat/ST-246 remedy. J Infect. 2024;88(2):203–5.
Koupenova M, Corkrey HA, Vitseva O, Tanriverdi Okay, Somasundaran M, Liu P, et al. SARS-CoV-2 initiates programmed cell loss of life in platelets. Circ Res. 2021;129(6):631–46.
Tsao CW, Aday AW, Almarzooq ZI, Alonso A, Beaton AZ, Bittencourt MS, et al. Coronary heart illness and stroke statistics-2022 replace: a report from the American Coronary heart Affiliation. Circulation. 2022;145(8):e153-639.
Anderson JL, Morrow DA. Acute myocardial infarction. N Engl J Med. 2017;376(21):2053–64.
Ibanez B, James S, Agewall S, Antunes MJ, Bucciarelli-Ducci C, Bueno H, et al. 2017 ESC Pointers for the administration of acute myocardial infarction in sufferers presenting with ST-segment elevation: The Process Drive for the administration of acute myocardial infarction in sufferers presenting with ST-segment elevation of the European Society of Cardiology (ESC). Eur Coronary heart J. 2018;39(2):119–77.
Wang J, Zhou H. Mitochondrial high quality management mechanisms as molecular targets in cardiac ischemia–reperfusion damage. Acta Pharm Sin B. 2020;10(10):1866–79.
Nicolas-Avila JA, Lechuga-Vieco AV, Esteban-Martinez L, Sanchez-Diaz M, Diaz-Garcia E, Santiago DJ, et al. A community of macrophages helps mitochondrial homeostasis within the coronary heart. Cell. 2020;183(1):94–109.
Music R, Dasgupta C, Mulder C, Zhang L. MicroRNA-210 controls mitochondrial metabolism and protects coronary heart operate in myocardial infarction. Circulation. 2022;145(15):1140–53.
Shen J, Zhang JH, Xiao H, Wu JM, He KM, Lv ZZ, et al. Mitochondria are transported alongside microtubules in membrane nanotubes to rescue distressed cardiomyocytes from apoptosis. Cell Dying Dis. 2018;9(2):81.
Zheng Y, Lang Y, Qi B, Li T. TSPAN4 and migrasomes in atherosclerosis regression correlated to myocardial infarction and pan-cancer development. Cell Adh Migr. 2023;17(1):14–9.
Gagat M, Zielinska W, Mikolajczyk Okay, Zabrzynski J, Krajewski A, Klimaszewska-Wisniewska A, et al. CRISPR-based activation of endogenous expression of TPM1 inhibits inflammatory response of main human coronary artery endothelial and clean muscle cells induced by recombinant human tumor necrosis issue alpha. Entrance Cell Dev Biol. 2021;9: 668032.
Wang YJ, Yang Okay, Wen Y, Wang P, Hu Y, Lai Y, et al. Screening and prognosis of heart problems utilizing synthetic intelligence-enabled cardiac magnetic resonance imaging. Nat Med. 2024;30(5):1471–80.
Bayes-Genis A, Docherty KF, Petrie MC, Januzzi JL, Mueller C, Anderson L, et al. Sensible algorithms for early prognosis of coronary heart failure and coronary heart stress utilizing NT-proBNP: a scientific consensus assertion from the Coronary heart Failure Affiliation of the ESC. Eur J Coronary heart Fail. 2023;25(11):1891–8.
Jansen F, Nickenig G, Werner N. Extracellular vesicles in heart problems: potential purposes in prognosis, prognosis, and epidemiology. Circ Res. 2017;120(10):1649–57.
Brush JJ, Sherbino J, Norman GR. Diagnostic reasoning in cardiovascular medication. BMJ. 2022;376: e64389.
Foster RR, Saleem MA, Mathieson PW, Bates DO, Harper SJ. Vascular endothelial progress issue and nephrin work together and cut back apoptosis in human podocytes. Am J Physiol Renal Physiol. 2005;288(1):F48-57.
Petermann A, Floege J. Podocyte harm leading to podocyturia: a possible diagnostic marker to evaluate glomerular illness exercise. Nephron Clin Pract. 2007;106(2):c61–6.
Pagtalunan ME, Miller PL, Leaping-Eagle S, Nelson RG, Myers BD, Rennke HG, et al. Podocyte loss and progressive glomerular damage in kind II diabetes. J Clin Make investments. 1997;99(2):342–8.
Steffes MW, Schmidt D, McCrery R, Basgen JM. Glomerular cell quantity in regular topics and in kind 1 diabetic sufferers. Kidney Int. 2001;59(6):2104–13.
Ivanova EA, Arcolino FO, Elmonem MA, Rastaldi MP, Giardino L, Cornelissen EM, et al. Cystinosin deficiency causes podocyte harm and loss related to elevated cell motility. Kidney Int. 2016;89(5):1037–48.
Widmeier E, Tan W, Airik M, Hildebrandt F. A small molecule screening to detect potential therapeutic targets in human podocytes. Am J Physiol Renal Physiol. 2017;312(1):F157–71.
Morrison EE, Bailey MA, Expensive JW. Renal extracellular vesicles: from physiology to scientific software. J Physiol. 2016;594(20):5735–48.
Abbasian N, Herbert KE, Pawluczyk I, Burton JO, Bevington A. Vesicles bearing presents: the purposeful significance of micro-RNA switch in extracellular vesicles in power kidney illness. Am J Physiol Renal Physiol. 2018;315(5):F1430–43.
Bikbov B, Purcell C, Levey AS, Smith M, Abdoli A, Abebe M,et al. International, regional, and nationwide burden of power kidney illness, 1990–2017: a scientific evaluation for the International Burden of Illness Examine 2017. Lancet. 2020;395(10225):709–33.
Erdbrugger U, Le TH. Extracellular vesicles in renal ailments: greater than novel biomarkers? J Am Soc Nephrol. 2016;27(1):12–26.
Ranghino A, Bruno S, Bussolati B, Moggio A, Dimuccio V, Tapparo M, et al. The consequences of glomerular and tubular renal progenitors and derived extracellular vesicles on restoration from acute kidney damage. Stem Cell Res Ther. 2017;8(1):24.
Burbano C, Gomez-Puerta JA, Munoz-Vahos C, Vanegas-Garcia A, Rojas M, Vasquez G, et al. HMGB1(+) microparticles current in urine are hallmarks of nephritis in sufferers with systemic lupus erythematosus. Eur J Immunol. 2019;49(2):323–35.
Chirackal RS, Jayachandran M, Wang X, Edeh S, Haskic Z, Perinpam M, et al. Urinary extracellular vesicle-associated MCP-1 and NGAL derived from particular nephron segments differ between calcium oxalate stone formers and controls. Am J Physiol Renal Physiol. 2019;317(6):F1475–82.
Ronco P, Beck L, Debiec H, Fervenza FC, Hou FF, Jha V, et al. Membranous nephropathy. Nat Rev Dis Primers. 2021;7(1):69.
Wang B, Fu YQ, Xie LJ, Cao JY, Yang M, Li M, et al. Measurement of urinary exosomal phospholipase A2 receptor is a delicate technique for prognosis of PLA2R-associated membranous nephropathy. Clin Kidney J. 2024;17(1): d191.
Pattrapornpisut P, Kulasingam V, Reich HN. Interpretation and scientific worth of serum anti-PLA2R-antibody testing. J Appl Lab Med. 2021;6(3):799–803.
Yang R, Zhang H, Chen S, Lou Okay, Zhou M, Zhang M, et al. Quantification of urinary podocyte-derived migrasomes for the prognosis of kidney illness. J Extracell Vesicles. 2024;13(6): e12460.
Babelova A, Jansen F, Sander Okay, Lohn M, Schafer L, Fork C, et al. Activation of Rac-1 and RhoA contributes to podocyte damage in power kidney illness. PLoS ONE. 2013;8(11): e80328.
Robins R, Baldwin C, Aoudjit L, Cote JF, Gupta IR, Takano T. Rac1 activation in podocytes induces the spectrum of nephrotic syndrome. Kidney Int. 2017;92(2):349–64.
Gee HY, Saisawat P, Ashraf S, Hurd TW, Vega-Warner V, Fang H, et al. ARHGDIA mutations trigger nephrotic syndrome by way of faulty RHO GTPase signaling. J Clin Make investments. 2013;123(8):3243–53.
Quenby S, Gallos ID, Dhillon-Smith RK, Podesek M, Stephenson MD, Fisher J, et al. Miscarriage issues: the epidemiological, bodily, psychological, and financial prices of early being pregnant loss. Lancet. 2021;397(10285):1658–67.
La X, Wang W, Zhang M, Liang L. Definition and a number of components of recurrent spontaneous abortion. Adv Exp Med Biol. 2021;1300:231–57.
Shahine L, Lathi R. Recurrent being pregnant loss: analysis and remedy. Obstet Gynecol Clin North Am. 2015;42(1):117–34.
Ragusa A, Svelato A, Santacroce C, Catalano P, Notarstefano V, Carnevali O, et al. Plasticenta: first proof of microplastics in human placenta. Environ Int. 2021;146: 106274.
Liu Z, Zhuan Q, Zhang L, Meng L, Fu X, Hou Y. Polystyrene microplastics induced feminine reproductive toxicity in mice. J Hazard Mater. 2022;424(Pt C): 127629.
Dong X, Liu X, Hou Q, Wang Z. From pure setting to animal tissues: A evaluate of microplastics (nanoplastics) translocation and hazards research. Sci Complete Environ. 2023;855: 158686.
Lu P, Liu R, Lu D, Xu Y, Yang X, Jiang Z, et al. Chemical screening identifies ROCK1 as a regulator of migrasome formation. Cell Discov. 2020;6(1):51.
Torpy JM, Glass TJ, Glass RM. JAMA affected person web page. Retinopathy JAMA. 2005;293(1):128.
Cho HY, Chung SE, Kim JI, Park KH, Kim SK, Kang SW. Spontaneous reattachment of rhegmatogenous retinal detachment. Ophthalmology. 2007;114(3):581–6.
Jin HD, Russell JF. Self-limiting bilateral foveal detachment after coup-contrecoup damage. Ophthalmology. 2023;130(2):197.
Katzeff BS. Acute-onset floaters and flashes and danger for retinal detachment. JAMA. 2010;303(14):1369–70.
Cui JZ, Chiu A, Maberley D, Ma P, Samad A, Matsubara JA. Stage specificity of novel progress issue expression throughout growth of proliferative vitreoretinopathy. Eye (London). 2007;21(2):200–8.
Ogata N, Nishikawa M, Nishimura T, Mitsuma Y, Matsumura M. Inverse ranges of pigment epithelium-derived issue and vascular endothelial progress issue within the vitreous of eyes with rhegmatogenous retinal detachment and proliferative vitreoretinopathy. AM J Ophthalmol. 2002;133(6):851–2.
Casaroli MR, Vilaro S. The position of fibronectin, laminin, vitronectin and their receptors on mobile adhesion in proliferative vitreoretinopathy. Make investments Ophthalmol Vis Sci. 1994;35(6):2791–803.
Moysidis SN, Thanos A, Vavvas DG. Mechanisms of irritation in proliferative vitreoretinopathy: from bench to bedside. Mediators Inflamm. 2012;2012: 815937.
Kaarniranta Okay, Xu H, Kauppinen A. Mechanistical retinal drug targets and challenges. Adv Drug Deliv Rev. 2018;126:177–84.
Manai F, Smedowski A, Kaarniranta Okay, Comincini S, Amadio M. Extracellular vesicles in degenerative retinal ailments: a brand new therapeutic paradigm. J Management Launch. 2024;365:448–68.
Muller-Eberhard HJ. Complement. Annu Rev Biochem. 1975;44:697–724.
West EE, Kolev M, Kemper C. Complement and the regulation of T cell responses. Annu Rev Immunol. 2018;36:309–38.
Wu Z, Cheung NV. T cell participating bispecific antibody (T-BsAb): from expertise to therapeutics. Pharmacol Ther. 2018;182:161–75.
Sergeeva A, Alatrash G, He H, Ruisaard Okay, Lu S, Wygant J, et al. An anti-PR1/HLA-A2 T-cell receptor-like antibody mediates complement-dependent cytotoxicity towards acute myeloid leukemia progenitor cells. Blood. 2011;117(16):4262–72.
Biffi A, Greenberg SM. Cerebral amyloid angiopathy: a scientific evaluate. J Clin Neurol. 2011;7(1):1–9.
Musiek ES, Holtzman DM. Three dimensions of the amyloid speculation: time, house and “wingmen.” Nat Neurosci. 2015;18(6):800–6.
Saito S, Yamamoto Y, Maki T, Hattori Y, Ito H, Mizuno Okay, et al. Taxifolin inhibits amyloid-beta oligomer formation and totally restores vascular integrity and reminiscence in cerebral amyloid angiopathy. Acta Neuropathol Commun. 2017;5(1):26.
Charidimou A, Martinez-Ramirez S, Reijmer YD, Oliveira-Filho J, Lauer A, Roongpiboonsopit D, et al. Complete magnetic resonance imaging burden of small vessel illness in cerebral amyloid angiopathy: an imaging-pathologic examine of idea validation. Jama Neurol. 2016;73(8):994–1001.
Grubman A, Choo XY, Chew G, Ouyang JF, Solar G, Croft NP, et al. Transcriptional signature in microglia related to Abeta plaque phagocytosis. Nat Commun. 2021;12(1):3015.
Chen SH, Tian DY, Shen YY, Cheng Y, Fan DY, Solar HL, et al. Amyloid-beta uptake by blood monocytes is lowered with ageing and Alzheimer’s illness. Transl Psychiatry. 2020;10(1):423.
Bogie J, Grajchen E, Wouters E, Corrales AG, Dierckx T, Vanherle S, et al. Stearoyl-CoA desaturase-1 impairs the reparative properties of macrophages and microglia within the mind. J Exp Med. 2020;217(5):e20191660.
Westendorp WF, Dames C, Nederkoorn PJ, Meisel A. Immunodepression, infections, and purposeful final result in ischemic stroke. Stroke. 2022;53(5):1438–48.
Faura J, Bustamante A, Miro-Mur F, Montaner J. Stroke-induced immunosuppression: implications for the prevention and prediction of post-stroke infections. J Neuroinflammation. 2021;18(1):127.
Suda S, Aoki J, Shimoyama T, Suzuki Okay, Sakamoto Y, Katano T, et al. Stroke-associated an infection independently predicts 3-month poor purposeful final result and mortality. J Neurol. 2018;265(2):370–5.
Bustamante A, Giralt D, Garcia-Berrocoso T, Rubiera M, Alvarez-Sabin J, Molina C, et al. The affect of post-stroke issues on in-hospital mortality is dependent upon stroke severity. Eur Stroke J. 2017;2(1):54–63.
Vermeij JD, Westendorp WF, Dippel DW, van de Beek D, Nederkoorn PJ. Antibiotic remedy for stopping infections in individuals with acute stroke. Cochrane Database Syst Rev. 2018;1(1):D8530.
Scott NA, Andrusaite A, Andersen P, Lawson M, Alcon-Giner C, Leclaire C, et al. Antibiotics induce sustained dysregulation of intestinal T cell immunity by perturbing macrophage homeostasis. Sci Transl Med. 2018;10(464):eaa04755.
Andrzejewska A, Dabrowska S, Lukomska B, Janowski M. Mesenchymal stem cells for neurological issues. Adv Sci (Weinh). 2021;8(7):2002944.
Wang L, Deng Z, Zhao Y, Yuan R, Yang M, Zhang Y, et al. Mesenchymal stem cells regulate activation of microglia cells to enhance hippocampal damage of warmth stroke rats. J Therm Biol. 2021;101: 103081.
Shi L, Huang H, Lu X, Yan X, Jiang X, Xu R, et al. Impact of human umbilical cord-derived mesenchymal stem cells on lung harm in extreme COVID-19 sufferers: a randomized, double-blind, placebo-controlled section 2 trial. Sign Transduct Goal Ther. 2021;6(1):58.
Li T, Su X, Lu P, Kang X, Hu M, Li C, et al. Bone marrow mesenchymal stem cell-derived dermcidin-containing migrasomes improve LC3-associated phagocytosis of pulmonary macrophages and defend towards post-stroke pneumonia. Adv Sci (Weinh). 2023;10(22): e2206432.
Schmidt-Pogoda A, Strecker JK, Liebmann M, Massoth C, Beuker C, Hansen U, et al. Dietary salt promotes ischemic mind damage and is related to parenchymal migrasome formation. PLoS ONE. 2018;13(12): e209871.
Pardridge WM. A historic evaluate of mind drug supply. Pharmaceutics. 2022;14(6):1283.
Rawal SU, Patel BM, Patel MM. New drug supply methods developed for mind focusing on. Medication. 2022;82(7):749–92.
Sissung TM, Figg WD. Stem cell clinics: danger of proliferation. Lancet Oncol. 2020;21(2):205–6.
Macia E, Boyden PA. Stem cell remedy is proarrhythmic. Circulation. 2009;119(13):1814–23.
Steele AN, MacArthur JW, Woo YJ. Stem cell remedy: therapeutic or hype? Why stem cell supply doesn’t work. Circ Res. 2017;120(12):1868–70.
Li Y, Bi X, Wu M, Chen X, Zhan W, Dong Z, et al. Adjusting the stiffness of a cell-free hydrogel system based mostly on tissue-specific extracellular matrix to optimize adipose tissue regeneration. Burns Trauma. 2023;11: d2.
Qin Y, Ge G, Yang P, Wang L, Qiao Y, Pan G, et al. An replace on adipose-derived stem cells for regenerative medication: the place problem meets alternative. Adv Sci (Weinh). 2023;10(20): e2207334.
Coulange ZA, Velier M, Arcani R, Abellan LM, Simoncini S, Benyamine A, et al. Adipose tissue and adipose-tissue-derived cell therapies for the remedy of the face and palms of sufferers affected by systemic sclerosis. Biomedicines. 2023;11(2):348.
Krastev TK, Schop SJ, Hommes J, Piatkowski A, van der Hulst R. Autologous fats switch to deal with fibrosis and scar-related situations: a scientific evaluate and meta-analysis. J Plast Reconstr Aesthet Surg. 2020;73(11):2033–48.
Kolle SF, Fischer-Nielsen A, Mathiasen AB, Elberg JJ, Oliveri RS, Glovinski PV, et al. Enrichment of autologous fats grafts with ex-vivo expanded adipose tissue-derived stem cells for graft survival: a randomised placebo-controlled trial. Lancet. 2013;382(9898):1113–20.
Butala P, Hazen A, Szpalski C, Sultan SM, Coleman SR, Warren SM. Endogenous stem cell remedy enhances fats graft survival. Plast Reconstr Surg. 2012;130(2):293–306.
Girousse A, Gil-Ortega M, Bourlier V, Bergeaud C, Sastourne-Arrey Q, Moro C, et al. The discharge of adipose stromal cells from subcutaneous adipose tissue regulates ectopic intramuscular adipocyte deposition. Cell Rep. 2019;27(2):323–33.
Majumdar R, Sixt M, Guardian CA. New paradigms within the institution and upkeep of gradients throughout directed cell migration. Curr Opin Cell Biol. 2014;30:33–40.
Lim Okay, Hyun YM, Lambert-Emo Okay, Capece T, Bae S, Miller R, et al. Neutrophil trails information influenza-specific CD8(+) T cells within the airways. Science. 2015;349(6252): a4352.
Luga V, Zhang L, Viloria-Petit AM, Ogunjimi AA, Inanlou MR, Chiu E, et al. Exosomes mediate stromal mobilization of autocrine Wnt-PCP signaling in breast most cancers cell migration. Cell. 2012;151(7):1542–56.
Jin ZB, Gao ML, Deng WL, Wu KC, Sugita S, Mandai M, et al. Stemming retinal regeneration with pluripotent stem cells. Prog Retin Eye Res. 2019;69:38–56.
Zhu Y, Ge J, Huang C, Liu H, Jiang H. Software of mesenchymal stem cell remedy for growing older frailty: from mechanisms to therapeutics. Theranostics. 2021;11(12):5675–85.
Al-Ghadban S, Artiles M, Bunnell BA. Adipose stem cells in regenerative medication: trying ahead. Entrance Bioeng Biotechnol. 2021;9: 837464.
Philips BJ, Grahovac TL, Valentin JE, Chung CW, Bliley JM, Pfeifer ME, et al. Prevalence of endogenous CD34+ adipose stem cells predicts human fats graft retention in a xenograft mannequin. Plast Reconstr Surg. 2013;132(4):845–58.
Suga H, Eto H, Aoi N, Kato H, Araki J, Doi Okay, et al. Adipose tissue transforming beneath ischemia: loss of life of adipocytes and activation of stem/progenitor cells. Plast Reconstr Surg. 2010;126(6):1911–23.
Deniz IA, Karbanova J, Wobus M, Bornhauser M, Wimberger P, Kuhlmann JD, et al. Mesenchymal stromal cell-associated migrasomes: a brand new supply of chemoattractant for cells of hematopoietic origin. Cell Commun Sign. 2023;21(1):36.
McIntosh Okay, Zvonic S, Garrett S, Mitchell JB, Floyd ZE, Hammill L, et al. The immunogenicity of human adipose-derived cells: temporal modifications in vitro. Stem Cells. 2006;24(5):1246–53.