Human Stem Cells Promote Liver Regeneration After Partial Hepatectomy in BALB/C Nude Mice

被引:11
|
作者
Wabitsch, Simon [1 ,2 ]
Benzing, Christian [1 ,2 ]
Krenzien, Felix [1 ,2 ]
Splith, Katrin [1 ,2 ]
Haber, Philipp Konstantin [1 ,2 ]
Arnold, Alexander [2 ,3 ]
Noesser, Maximilian [1 ,2 ]
Kamali, Can [1 ,2 ]
Hermann, Felix [4 ]
Guenther, Christiane [4 ]
Hirsch, Daniela [4 ]
Sauer, Igor M. [1 ,2 ]
Pratschke, Johann [1 ,2 ]
Schmelzle, Moritz [1 ,2 ]
机构
[1] Charite, Campus Charite Mitte, Dept Surg, Augustenburger Pl 1, D-13353 Berlin, Germany
[2] Charite, Campus Virchow Klinikum, Augustenburger Pl 1, D-13353 Berlin, Germany
[3] Charite, Campus Charite Mitte, Dept Pathol, Berlin, Germany
[4] Apceth Biopharma GmbH, Munich, Germany
关键词
Partial hepatectomy; Liver regeneration; Hepatocyte proliferation; Stem cells; Mesenchymal stem cells; PORTAL-VEIN EMBOLIZATION; HEPATIC-FAILURE; STROMAL CELLS; INFUSION; INCREASE; ADULT; MOUSE; MOBILIZATION; DYSFUNCTION; INHIBITION;
D O I
10.1016/j.jss.2019.02.010
中图分类号
R61 [外科手术学];
学科分类号
摘要
Background: Mesenchymal stem cells (MSCs) have been suggested to augment liver regeneration after surgically and pharmacologically induced liver failure. To further investigate this we processed human bone marrow-derived MSC according to good manufacturing practice (GMP) and tested those cells for their modulatory capacities of metabolic alterations and liver regeneration after partial hepatectomy in BALB/c nude mice. Methods: Human MSCs were obtained by bone marrow aspiration of healthy donors as in a previously described GMP process. Transgenic GFP-MSCs were administered i.p. 24 h after 70% hepatectomy in BALB/c nude mice, whereas control mice received phosphate-buffered saline. Mice were sacrificed 2, 3, and 5 d after partial hepatectomy. Blood and organs were harvested and metabolic alterations as well as liver regeneration subsequently assessed by liver function tests, multianalyte profiling immunoassays, histology, and immunostaining. Results: Hepatocyte and sinusoidal endothelial cell proliferation were significantly increased after partial hepatectomy in mice receiving MSC compared to control mice (Hepatocyte postoperative day 3, P < 0.01; endothelial cell postoperative day 5, P < 0.05). Hepatocyte fat accumulation correlated inversely with hepatocyte proliferation (r(2) = 0.4064, P < 0.01) 2 d after partial hepatectomy, with mice receiving MSC being protected from severe fat accumulation. No GFP-positive cells could be detected in the samples. Serum levels of IL-6, HGF, and IL-10 were significantly decreased at day 3 in mice receiving MSC when compared to control mice (P < 0.05). Relative body weight loss was significantly attenuated after partial hepatectomy in mice receiving MSC (2 d and 3 d, both P < 0.001) with a trend toward a faster relative restoration of liver weight, when compared to control mice. Conclusions: Human bone marrow-derived MSC attenuate metabolic alterations and improve liver regeneration after partial hepatectomy in BALB/c nude mice. Obtained results using GMP-processed human MSC suggest functional links between fat accumulation and hepatocyte proliferation, without any evidence for cellular homing. This study using GMP-proceeded MSC has important regulatory implications for an urgently needed translation into a clinical trial. (C) 2019 Elsevier Inc. All rights reserved.
引用
收藏
页码:191 / 200
页数:10
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