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Liver Regeneration by Hematopoietic Stem Cells: Have We Reached the End of the Road?

Thumbnail
Auteur
Siapati E.K., Roubelakis M.G., Vassilopoulos G.
Date
2022
Language
en
DOI
10.3390/cells11152312
Sujet
alanine aminotransferase
albumin
alpha fetoprotein
aspartate aminotransferase
bilirubin
carrier protein
colony stimulating factor 1
cytokine
fibroblast growth factor
fms related receptor tyrosine kinase 3 ligand
fusion protein
granulocyte macrophage colony stimulating factor
interleukin 6
scatter factor
somatomedin C
stem cell factor
stromal cell derived factor 1
thrombocyte factor 4
thrombopoietin
transforming growth factor beta
tumor necrosis factor
unclassified drug
vasculotropin
Wnt protein
arteriole
bone marrow
cell transdifferentiation
Child Pugh score
clinical trial (topic)
colony forming unit GM
dendritic cell
embryo development
end stage liver disease
endoderm
endothelium cell
extramedullary hematopoiesis
fetus liver
hematopoietic stem cell
hepatic stellate cell
hepatobiliary system
hepatocyte transplantation
human
human cell
human embryonic stem cell
international normalized ratio
Kupffer cell
liver
liver cirrhosis
liver disease
liver regeneration
liver sinusoid
lymphoid progenitor cell
macrophage
megakaryocyte erythroid progenitor
mesodermal cell
mobilization
Model For End Stage Liver Disease Score
myeloid progenitor cell
paracrine signaling
prothrombin time
randomized controlled trial (topic)
Review
stem cell niche
stem cell transplantation
adult
hematopoietic stem cell
liver disease
liver regeneration
liver transplantation
living donor
Adult
Hematopoietic Stem Cells
Humans
Liver Diseases
Liver Regeneration
Liver Transplantation
Living Donors
MDPI
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Résumé
The 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.
URI
http://hdl.handle.net/11615/78953
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  • Δημοσιεύσεις σε περιοδικά, συνέδρια, κεφάλαια βιβλίων κλπ. [19735]

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