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dc.creatorSiapati E.K., Roubelakis M.G., Vassilopoulos G.en
dc.date.accessioned2023-01-31T09:55:48Z
dc.date.available2023-01-31T09:55:48Z
dc.date.issued2022
dc.identifier10.3390/cells11152312
dc.identifier.issn20734409
dc.identifier.urihttp://hdl.handle.net/11615/78953
dc.description.abstractThe liver is the organ with the highest regenerative capacity in the human body. However, various insults, including viral infections, alcohol or drug abuse, and metabolic overload, may cause chronic inflammation and fibrosis, leading to irreversible liver dysfunction. Despite advances in surgery and pharmacological treatments, liver diseases remain a leading cause of death worldwide. To address the shortage of donor liver organs for orthotopic liver transplantation, cell therapy in liver disease has emerged as a promising regenerative treatment. Sources include primary hepatocytes or functional hepatocytes generated from the reprogramming of induced pluripotent stem cells (iPSC). Different types of stem cells have also been employed for transplantation to trigger regeneration, including hematopoietic stem cells (HSCs), mesenchymal stromal cells (MSCs), endothelial progenitor cells (EPCs) as well as adult and fetal liver progenitor cells. HSCs, usually defined by the expression of CD34 and CD133, and MSCs, defined by the expression of CD105, CD73, and CD90, are attractive sources due to their autologous nature, ease of isolation and cryopreservation. The present review focuses on the use of bone marrow HSCs for liver regeneration, presenting evidence for an ongoing crosstalk between the hematopoietic and the hepatic system. This relationship commences during embryogenesis when the fetal liver emerges as the crossroads between the two systems converging the presence of different origins of cells (mesoderm and endoderm) in the same organ. Ample evidence indicates that the fetal liver supports the maturation and expansion of HSCs during development but also later on in life. Moreover, the fact that the adult liver remains one of the few sites for extramedullary hematopoiesis—albeit pathological—suggests that this relationship between the two systems is ongoing. Can, however, the hematopoietic system offer similar support to the liver? The majority of clinical studies using hematopoietic cell transplantation in patients with liver disease report favourable observations. The underlying mechanism—whether paracrine, fusion or transdifferentiation or a combination of the three—remains to be confirmed. © 2022 by the authors.en
dc.language.isoenen
dc.sourceCellsen
dc.source.urihttps://www.scopus.com/inward/record.uri?eid=2-s2.0-85136343178&doi=10.3390%2fcells11152312&partnerID=40&md5=d2b99301e49bb9a363b7bb4750c098a1
dc.subjectalanine aminotransferaseen
dc.subjectalbuminen
dc.subjectalpha fetoproteinen
dc.subjectaspartate aminotransferaseen
dc.subjectbilirubinen
dc.subjectcarrier proteinen
dc.subjectcolony stimulating factor 1en
dc.subjectcytokineen
dc.subjectfibroblast growth factoren
dc.subjectfms related receptor tyrosine kinase 3 liganden
dc.subjectfusion proteinen
dc.subjectgranulocyte macrophage colony stimulating factoren
dc.subjectinterleukin 6en
dc.subjectscatter factoren
dc.subjectsomatomedin Cen
dc.subjectstem cell factoren
dc.subjectstromal cell derived factor 1en
dc.subjectthrombocyte factor 4en
dc.subjectthrombopoietinen
dc.subjecttransforming growth factor betaen
dc.subjecttumor necrosis factoren
dc.subjectunclassified drugen
dc.subjectvasculotropinen
dc.subjectWnt proteinen
dc.subjectarterioleen
dc.subjectbone marrowen
dc.subjectcell transdifferentiationen
dc.subjectChild Pugh scoreen
dc.subjectclinical trial (topic)en
dc.subjectcolony forming unit GMen
dc.subjectdendritic cellen
dc.subjectembryo developmenten
dc.subjectend stage liver diseaseen
dc.subjectendodermen
dc.subjectendothelium cellen
dc.subjectextramedullary hematopoiesisen
dc.subjectfetus liveren
dc.subjecthematopoietic stem cellen
dc.subjecthepatic stellate cellen
dc.subjecthepatobiliary systemen
dc.subjecthepatocyte transplantationen
dc.subjecthumanen
dc.subjecthuman cellen
dc.subjecthuman embryonic stem cellen
dc.subjectinternational normalized ratioen
dc.subjectKupffer cellen
dc.subjectliveren
dc.subjectliver cirrhosisen
dc.subjectliver diseaseen
dc.subjectliver regenerationen
dc.subjectliver sinusoiden
dc.subjectlymphoid progenitor cellen
dc.subjectmacrophageen
dc.subjectmegakaryocyte erythroid progenitoren
dc.subjectmesodermal cellen
dc.subjectmobilizationen
dc.subjectModel For End Stage Liver Disease Scoreen
dc.subjectmyeloid progenitor cellen
dc.subjectparacrine signalingen
dc.subjectprothrombin timeen
dc.subjectrandomized controlled trial (topic)en
dc.subjectReviewen
dc.subjectstem cell nicheen
dc.subjectstem cell transplantationen
dc.subjectadulten
dc.subjecthematopoietic stem cellen
dc.subjectliver diseaseen
dc.subjectliver regenerationen
dc.subjectliver transplantationen
dc.subjectliving donoren
dc.subjectAdulten
dc.subjectHematopoietic Stem Cellsen
dc.subjectHumansen
dc.subjectLiver Diseasesen
dc.subjectLiver Regenerationen
dc.subjectLiver Transplantationen
dc.subjectLiving Donorsen
dc.subjectMDPIen
dc.titleLiver Regeneration by Hematopoietic Stem Cells: Have We Reached the End of the Road?en
dc.typeotheren


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