Skip to main content
Erschienen in: Langenbeck's Archives of Surgery 5/2016

19.04.2016 | ORIGINAL ARTICLE

Effects of mesenchymal stem cells and VEGF on liver regeneration following major resection

Erschienen in: Langenbeck's Archives of Surgery | Ausgabe 5/2016

Einloggen, um Zugang zu erhalten

Abstract

Purpose

The study aims to determine the effects of mesenchymal stem cell (MSC) therapy and a combination therapy of MSCs transfected with vascular endothelial growth factor (VEGF) for liver regeneration after major resection.

Methods

Thirty-eight rats were divided into four groups: group 1: control (sham operation); group 2: control (70 % hepatic resection); group 3: 70 % hepatic resection + systemically transplanted MSCs; and group 4: 70 % hepatic resection + systemically transplanted MSCs transfected with the VEGF gene. MSCs were injected via the portal vein route in study groups 3 and 4. Expression levels of VEGF, fibroblast growth factor (FGF), platelet-derived growth factor (PDGF), epidermal growth factor (EGF), transforming growth factor (TGF), hepatocyte growth factor (HGF), and augmenter of liver regeneration (ALR) were analyzed in the remnant liver tissue. We investigated the levels of angiogenic factors, VEGF-receptor, angiopoietin-1 (Angpt1) and Angpt2. Biochemical parameters of liver function in blood samples were measured and a histologic assessment of the livers was performed. The postoperative liver weight and volume of each rat were measured 14 days after surgery.

Results

The expression levels of all measured growth factors were significantly increased in groups 3 and 4 compared to the control groups. The levels of Angpt1 and Angpt2 correlated with levels of VEGF and thus were also significantly higher in the study groups. There were significant differences between the estimated liver weights and volumes of group 4 and the resected controls in group 2. With the exception of portal inflammation, levels of all histological parameters were observed to be higher in MSC-treated groups when compared with the resected controls in group 2.

Conclusions

Transplanted stem cells and MSCs transfected with VEGF significantly accelerated many parameters of the healing process following major hepatic resection. After the injection of MSCs and VEGF-transfected MSCs into the portal vein following liver resection, they were engrafted in the liver. They increased bile duct and liver hepatocyte proliferation, and secreted many growth factors including HGF, TGFβ, VEGF, PDGF, EGF, and FGF via paracrine effects. These effects support liver function, regeneration, and liver volume/weight.
Literatur
1.
Zurück zum Zitat Makino H, Shimizu H, Ito H, Kimura F, Ambiru S, Togawa A, Ohtsuka M, Yoshidome H, Kato A, Yoshitomi H, Sawada S, Miyazaki M (2006) Changes in growth factor and cytokine expression in biliary obstructed rat liver and their relationship with delayed liver regeneration after partial hepatectomy. World J Gastroenterol 13:2053–2059CrossRef Makino H, Shimizu H, Ito H, Kimura F, Ambiru S, Togawa A, Ohtsuka M, Yoshidome H, Kato A, Yoshitomi H, Sawada S, Miyazaki M (2006) Changes in growth factor and cytokine expression in biliary obstructed rat liver and their relationship with delayed liver regeneration after partial hepatectomy. World J Gastroenterol 13:2053–2059CrossRef
2.
Zurück zum Zitat Blumgart LH (2007) Surgery of the liver, biliary tract, and pancreas. In: Blumgart LH, Belghiti J (eds) Liver resection for benign disease and for liver and biliary tumors. Fourth Edition, Vol:2, Philadelphia. 1341–1405 Blumgart LH (2007) Surgery of the liver, biliary tract, and pancreas. In: Blumgart LH, Belghiti J (eds) Liver resection for benign disease and for liver and biliary tumors. Fourth Edition, Vol:2, Philadelphia. 1341–1405
3.
Zurück zum Zitat Puglisi MA, Tesori V, Lattanzi W, Piscaglia AC, Gasbarrini GB, D’Ugo DM, Gasbarrini A (2011) Therapeutic implications of mesenchymal stem cells in liver injury. J Biomed Biotechnol 2011:860578 Puglisi MA, Tesori V, Lattanzi W, Piscaglia AC, Gasbarrini GB, D’Ugo DM, Gasbarrini A (2011) Therapeutic implications of mesenchymal stem cells in liver injury. J Biomed Biotechnol 2011:860578
4.
Zurück zum Zitat Ghaedi M, Tuleuova N, Zern AM, Wu J, Revzin A (2011) Bottom-up signaling from HGF-containing surfaces promoteshepatic differentiation of mesenchymal stem cells. Biochem Biophys Res Commun 2:295–300CrossRef Ghaedi M, Tuleuova N, Zern AM, Wu J, Revzin A (2011) Bottom-up signaling from HGF-containing surfaces promoteshepatic differentiation of mesenchymal stem cells. Biochem Biophys Res Commun 2:295–300CrossRef
5.
Zurück zum Zitat Wu BX, Tao R (2012) Hepatocyte differentiation of mesenchymal stem cells. Hepatobiliary Pancreat Dis Int 11:360–371CrossRefPubMed Wu BX, Tao R (2012) Hepatocyte differentiation of mesenchymal stem cells. Hepatobiliary Pancreat Dis Int 11:360–371CrossRefPubMed
6.
Zurück zum Zitat Shimizu H, Mitsuhashi N, Ohtsuka M, Ito H, Kimura F, Ambiru S, Togawa A, Yoshidome H, Kato A, Miyazaki M (2005) Vascular endothelial growth factor and angiopoietins regulate sinusoidal regeneration and remodeling after partial hepatectomy in rats. World J Gastroenterol 46:7254–7260CrossRef Shimizu H, Mitsuhashi N, Ohtsuka M, Ito H, Kimura F, Ambiru S, Togawa A, Yoshidome H, Kato A, Miyazaki M (2005) Vascular endothelial growth factor and angiopoietins regulate sinusoidal regeneration and remodeling after partial hepatectomy in rats. World J Gastroenterol 46:7254–7260CrossRef
8.
Zurück zum Zitat Duncan WA, Dorrell C, Grompe M (2009) Stem cells and liver regeneration. Gastroenterology 2:466–481CrossRef Duncan WA, Dorrell C, Grompe M (2009) Stem cells and liver regeneration. Gastroenterology 2:466–481CrossRef
9.
Zurück zum Zitat Burra P, Debora B, Ciccocippo R, Marra F, Piscaglia CA, Porretti L, Gasbarrini A, Russo PF (2011) Therapeutic application of stem cells in gastroenterology: an up-date. World J Gastroenterol 34:3870–3880CrossRef Burra P, Debora B, Ciccocippo R, Marra F, Piscaglia CA, Porretti L, Gasbarrini A, Russo PF (2011) Therapeutic application of stem cells in gastroenterology: an up-date. World J Gastroenterol 34:3870–3880CrossRef
10.
Zurück zum Zitat Hayashi Y, Tsujii S, Tsujii M, Nishida T, Ishii S, Lijima H, Nakamura T, Eguchi H, Miyoshi E, Hayashi N, Kawano S (2008) Topical implantation of mesenchymal stem cells has beneficial effects on healing of experimental colitis in rats. J Pharmacol Exp Ther 326:523–531CrossRefPubMed Hayashi Y, Tsujii S, Tsujii M, Nishida T, Ishii S, Lijima H, Nakamura T, Eguchi H, Miyoshi E, Hayashi N, Kawano S (2008) Topical implantation of mesenchymal stem cells has beneficial effects on healing of experimental colitis in rats. J Pharmacol Exp Ther 326:523–531CrossRefPubMed
11.
Zurück zum Zitat Chan PB, Hui YT, Yeung WC, Li J, Mo I, Chan GF (2007) Self-assembled collagen-human mesenchymal stem cell microspheres for regenerative medicine. Biomaterials 28:4652–4666CrossRefPubMed Chan PB, Hui YT, Yeung WC, Li J, Mo I, Chan GF (2007) Self-assembled collagen-human mesenchymal stem cell microspheres for regenerative medicine. Biomaterials 28:4652–4666CrossRefPubMed
12.
Zurück zum Zitat Markel AT, Crisostomo RP, Lahm T, Novotny MN, Rescoria JF, Tector JA, Meldrum RD (2008) Stem cells as a potential future treatment of pediatric intestinal disorders. J Pediatr Surg 11:1953–1963CrossRef Markel AT, Crisostomo RP, Lahm T, Novotny MN, Rescoria JF, Tector JA, Meldrum RD (2008) Stem cells as a potential future treatment of pediatric intestinal disorders. J Pediatr Surg 11:1953–1963CrossRef
13.
Zurück zum Zitat Enestvedt KC, Hosack L, Winn RS, Diggs SB, Uchida B, O’Rourke WR, Jobe AB (2008) VEGF gene therapy augments localized angiogenesis and promotes anastomic wound healing: a pilot study in a clinically relevant animal model. J Gastrointest Surg 12:1762–1772CrossRefPubMed Enestvedt KC, Hosack L, Winn RS, Diggs SB, Uchida B, O’Rourke WR, Jobe AB (2008) VEGF gene therapy augments localized angiogenesis and promotes anastomic wound healing: a pilot study in a clinically relevant animal model. J Gastrointest Surg 12:1762–1772CrossRefPubMed
14.
15.
Zurück zum Zitat Werner S, Grose R (2003) Regulation of wound healing by growth factors and cytokines. Physiol Rev 83:835–860PubMed Werner S, Grose R (2003) Regulation of wound healing by growth factors and cytokines. Physiol Rev 83:835–860PubMed
16.
Zurück zum Zitat Shimuzu H, Miyazaki M, Wakabayashi Y, Mitsuhashi N, Kato A, Ito H, Nakagawa K, Yoshidome H, Kataoka M, Nakajima N (2001) Vascular endothelial growth factor secreted by replicating hepatocytes induces sinusoidal endothelial cell proliferation during regeneration after partial hepatectomy in rats. J Hepatol 34:683–689CrossRef Shimuzu H, Miyazaki M, Wakabayashi Y, Mitsuhashi N, Kato A, Ito H, Nakagawa K, Yoshidome H, Kataoka M, Nakajima N (2001) Vascular endothelial growth factor secreted by replicating hepatocytes induces sinusoidal endothelial cell proliferation during regeneration after partial hepatectomy in rats. J Hepatol 34:683–689CrossRef
17.
Zurück zum Zitat Martins PN, Theruvath PT, Neuhaus P (2007) Rodent models of partial hepatectomies. Liver Int 3–11 Martins PN, Theruvath PT, Neuhaus P (2007) Rodent models of partial hepatectomies. Liver Int 3–11
18.
Zurück zum Zitat Greene AK, Puder M (2003) Partial hepatectomy in the mouse: technique and perioperative management. J Investig Surg 16:99–102CrossRef Greene AK, Puder M (2003) Partial hepatectomy in the mouse: technique and perioperative management. J Investig Surg 16:99–102CrossRef
19.
Zurück zum Zitat Best J, Dolle L, Manka P, Coombes J, Grunsven AL, Syn W (2013) Role of liver progenitors in acute liver injury. Front Physiol 4:1–8CrossRef Best J, Dolle L, Manka P, Coombes J, Grunsven AL, Syn W (2013) Role of liver progenitors in acute liver injury. Front Physiol 4:1–8CrossRef
20.
Zurück zum Zitat Cantz T, Manns PM, Ott M (2008) Stem cells in liver regeneration and therapy. Cell Tissue Res 331:271–282CrossRefPubMed Cantz T, Manns PM, Ott M (2008) Stem cells in liver regeneration and therapy. Cell Tissue Res 331:271–282CrossRefPubMed
21.
Zurück zum Zitat Chen WX, Zhu JD, Ju LY, Zhou FS (2012) Therapeutic effect of transplanting magnetically labeled bone marrow stromal stem cells in a liver injury rat model with 70%-hepatectomy. Med Sci Monit 10:375–382 Chen WX, Zhu JD, Ju LY, Zhou FS (2012) Therapeutic effect of transplanting magnetically labeled bone marrow stromal stem cells in a liver injury rat model with 70%-hepatectomy. Med Sci Monit 10:375–382
24.
Zurück zum Zitat Tanimuzu N, Miyajima A (2007) A molecular mechanism of liver development and regeneration. Int Rev Cytol 259:1–48CrossRef Tanimuzu N, Miyajima A (2007) A molecular mechanism of liver development and regeneration. Int Rev Cytol 259:1–48CrossRef
25.
Zurück zum Zitat Ding SB, Nolan JD, Butler MJ et al (2010) Inductive angiocrine signals from sinusoidal endothelium are required for liver regeneration. Nature 468(7321):310–315CrossRefPubMedPubMedCentral Ding SB, Nolan JD, Butler MJ et al (2010) Inductive angiocrine signals from sinusoidal endothelium are required for liver regeneration. Nature 468(7321):310–315CrossRefPubMedPubMedCentral
26.
Zurück zum Zitat Fausto N (2004) Liver regeneration and repair: hepatocytes, progenitor cells, and stem cells. Hepatology 39:1477–1487CrossRefPubMed Fausto N (2004) Liver regeneration and repair: hepatocytes, progenitor cells, and stem cells. Hepatology 39:1477–1487CrossRefPubMed
27.
Zurück zum Zitat Kallis YN, Alison MR, Forbes SJ (2007) Bone marrow stem cells and liver disease. Gut England 716–724 Kallis YN, Alison MR, Forbes SJ (2007) Bone marrow stem cells and liver disease. Gut England 716–724
28.
Zurück zum Zitat Ren G, Chen X, Dong F, Li W, Ren X, Zhang Y, Shi Y (2012) Concise review: mesenchymal stem cells and translational medicine: emerging issues. Stem Cells Transl Med 1:51–58CrossRefPubMed Ren G, Chen X, Dong F, Li W, Ren X, Zhang Y, Shi Y (2012) Concise review: mesenchymal stem cells and translational medicine: emerging issues. Stem Cells Transl Med 1:51–58CrossRefPubMed
29.
Zurück zum Zitat Crisostomo PR, Wang Y, Merkel TA et al (2008) Human mesenchymal stem cells stimulated by TNF-α, LPS, or hypoxia produce growth factors by NF-kB but not JNK-dependent mechanism. Am J Physiol Cell Physiol 294:675–682CrossRef Crisostomo PR, Wang Y, Merkel TA et al (2008) Human mesenchymal stem cells stimulated by TNF-α, LPS, or hypoxia produce growth factors by NF-kB but not JNK-dependent mechanism. Am J Physiol Cell Physiol 294:675–682CrossRef
30.
Zurück zum Zitat Caplan AI, Dennis JE (2006) Mesenchymal stem cells as trophic mediators. J Cell Biochem 98:1076–1084CrossRefPubMed Caplan AI, Dennis JE (2006) Mesenchymal stem cells as trophic mediators. J Cell Biochem 98:1076–1084CrossRefPubMed
31.
Zurück zum Zitat Shibuya M (2013) VEGF-VEGFR signals in health and disease. Biomol Ther 22(1):1–9CrossRef Shibuya M (2013) VEGF-VEGFR signals in health and disease. Biomol Ther 22(1):1–9CrossRef
32.
Zurück zum Zitat Shibuya M (2013) Vascular endothelial growth factor and its receptor system: physiological functions in angiogenesis and pathological roles in various diseases. J Biochem 153(1):13–19CrossRefPubMed Shibuya M (2013) Vascular endothelial growth factor and its receptor system: physiological functions in angiogenesis and pathological roles in various diseases. J Biochem 153(1):13–19CrossRefPubMed
33.
Zurück zum Zitat Karkkainen MJ, Petrova TV (2000) Vascular endothelial growth factor receptors in the regulation of angiogenesis and lymphangiogenesis. Oncogene 19(49):5598–5605CrossRefPubMed Karkkainen MJ, Petrova TV (2000) Vascular endothelial growth factor receptors in the regulation of angiogenesis and lymphangiogenesis. Oncogene 19(49):5598–5605CrossRefPubMed
34.
Zurück zum Zitat Heidaran MA, Pierce JH, Jensen RA et al (1990) Chimeric alpha- and - beta platelet derived growth factor receptors define three immunoglobulin-like domains of the alpha-PDGF receptor that determine PDGF-AA binding specificity. J Biol Chem 265(31):18741–4PubMed Heidaran MA, Pierce JH, Jensen RA et al (1990) Chimeric alpha- and - beta platelet derived growth factor receptors define three immunoglobulin-like domains of the alpha-PDGF receptor that determine PDGF-AA binding specificity. J Biol Chem 265(31):18741–4PubMed
35.
Zurück zum Zitat Michalopoulos KG (2010) Liver regeneration after partial hepatectomy: critical analysis of mechanistic dilemmas. AJP 176(1):2–13PubMedPubMedCentral Michalopoulos KG (2010) Liver regeneration after partial hepatectomy: critical analysis of mechanistic dilemmas. AJP 176(1):2–13PubMedPubMedCentral
36.
Zurück zum Zitat Francavilla A, Hagiya M, Porter KA, Polimeno L, Ihara I, Starzl TE (1994) Augmenter of liver regeneration: its place in the universe of hepatic growth factors. Hepatology 20:747–757CrossRefPubMed Francavilla A, Hagiya M, Porter KA, Polimeno L, Ihara I, Starzl TE (1994) Augmenter of liver regeneration: its place in the universe of hepatic growth factors. Hepatology 20:747–757CrossRefPubMed
37.
Zurück zum Zitat Gandhi CR, Kuddus R, Subbotin VM, Prelich J, Murase N, Rao AS, Nalesnik MA, Watkins SC, Deleo A, Trucco M, Starzl TE (1999) A fresh look at augmenter of liver regeneration in rats. Hepatology 29:1435–1445CrossRefPubMedPubMedCentral Gandhi CR, Kuddus R, Subbotin VM, Prelich J, Murase N, Rao AS, Nalesnik MA, Watkins SC, Deleo A, Trucco M, Starzl TE (1999) A fresh look at augmenter of liver regeneration in rats. Hepatology 29:1435–1445CrossRefPubMedPubMedCentral
38.
Zurück zum Zitat Gandhi CR, Murase N, Starzl TE (2010) Cholera toxin-sensitive GTP-binding protein-coupled activation of augmenter of liver regeneration (ALR) receptor and its function in rat Kupffer cells. J Cell Physiol 222:365–373CrossRefPubMedPubMedCentral Gandhi CR, Murase N, Starzl TE (2010) Cholera toxin-sensitive GTP-binding protein-coupled activation of augmenter of liver regeneration (ALR) receptor and its function in rat Kupffer cells. J Cell Physiol 222:365–373CrossRefPubMedPubMedCentral
39.
Zurück zum Zitat Balber AE (2011) Concise review: aldehyde dehydrogenase bright stem and progenitor cell populations from normal tissues: characteristics, activities, and emerging uses in regenerative medicine. Stem Cells 29(4):570–575CrossRefPubMed Balber AE (2011) Concise review: aldehyde dehydrogenase bright stem and progenitor cell populations from normal tissues: characteristics, activities, and emerging uses in regenerative medicine. Stem Cells 29(4):570–575CrossRefPubMed
40.
Zurück zum Zitat Hematti P (2008) Role of mesenchymal stromal cells in solid organ transplantation. Transplant Rev 22(4):262–273CrossRef Hematti P (2008) Role of mesenchymal stromal cells in solid organ transplantation. Transplant Rev 22(4):262–273CrossRef
41.
Zurück zum Zitat Kuo TK, Hung SP, Chuang CH et al (2008) Stem cell therapy for liver disease: parameters governing the success of using bone marrow mesenchymal stem cells. Gastroenterology 134:2111–2121CrossRefPubMedPubMedCentral Kuo TK, Hung SP, Chuang CH et al (2008) Stem cell therapy for liver disease: parameters governing the success of using bone marrow mesenchymal stem cells. Gastroenterology 134:2111–2121CrossRefPubMedPubMedCentral
42.
Zurück zum Zitat Banas A, Teratani T, Yamamoto Y et al (2009) Rapid hepatic fate specification of adipose-derived stem cells and their therapeutic potential for liver failure. J Gastroenterol Hepatol 24:70–77CrossRefPubMed Banas A, Teratani T, Yamamoto Y et al (2009) Rapid hepatic fate specification of adipose-derived stem cells and their therapeutic potential for liver failure. J Gastroenterol Hepatol 24:70–77CrossRefPubMed
43.
Zurück zum Zitat Carvelho AB, Quintanilha LF, Dias JV et al (2008) Bone marrow multipotent mesenchymal stromal cells do not reduce fibrosis or improve function in a rat model of severe chronic liver injury. Stem Cells 26:1307–1314CrossRef Carvelho AB, Quintanilha LF, Dias JV et al (2008) Bone marrow multipotent mesenchymal stromal cells do not reduce fibrosis or improve function in a rat model of severe chronic liver injury. Stem Cells 26:1307–1314CrossRef
Metadaten
Titel
Effects of mesenchymal stem cells and VEGF on liver regeneration following major resection
Publikationsdatum
19.04.2016
Erschienen in
Langenbeck's Archives of Surgery / Ausgabe 5/2016
Print ISSN: 1435-2443
Elektronische ISSN: 1435-2451
DOI
https://doi.org/10.1007/s00423-016-1380-9

Weitere Artikel der Ausgabe 5/2016

Langenbeck's Archives of Surgery 5/2016 Zur Ausgabe

Update Chirurgie

Bestellen Sie unseren Fach-Newsletter und bleiben Sie gut informiert.

S3-Leitlinie „Diagnostik und Therapie des Karpaltunnelsyndroms“

CME: 2 Punkte

Prof. Dr. med. Gregor Antoniadis Das Karpaltunnelsyndrom ist die häufigste Kompressionsneuropathie peripherer Nerven. Obwohl die Anamnese mit dem nächtlichen Einschlafen der Hand (Brachialgia parästhetica nocturna) sehr typisch ist, ist eine klinisch-neurologische Untersuchung und Elektroneurografie in manchen Fällen auch eine Neurosonografie erforderlich. Im Anfangsstadium sind konservative Maßnahmen (Handgelenksschiene, Ergotherapie) empfehlenswert. Bei nicht Ansprechen der konservativen Therapie oder Auftreten von neurologischen Ausfällen ist eine Dekompression des N. medianus am Karpaltunnel indiziert.

Prof. Dr. med. Gregor Antoniadis
Berufsverband der Deutschen Chirurgie e.V.

S2e-Leitlinie „Distale Radiusfraktur“

CME: 2 Punkte

Dr. med. Benjamin Meyknecht, PD Dr. med. Oliver Pieske Das Webinar S2e-Leitlinie „Distale Radiusfraktur“ beschäftigt sich mit Fragen und Antworten zu Diagnostik und Klassifikation sowie Möglichkeiten des Ausschlusses von Zusatzverletzungen. Die Referenten erläutern, welche Frakturen konservativ behandelt werden können und wie. Das Webinar beantwortet die Frage nach aktuellen operativen Therapiekonzepten: Welcher Zugang, welches Osteosynthesematerial? Auf was muss bei der Nachbehandlung der distalen Radiusfraktur geachtet werden?

PD Dr. med. Oliver Pieske
Dr. med. Benjamin Meyknecht
Berufsverband der Deutschen Chirurgie e.V.

S1-Leitlinie „Empfehlungen zur Therapie der akuten Appendizitis bei Erwachsenen“

CME: 2 Punkte

Dr. med. Mihailo Andric
Inhalte des Webinars zur S1-Leitlinie „Empfehlungen zur Therapie der akuten Appendizitis bei Erwachsenen“ sind die Darstellung des Projektes und des Erstellungswegs zur S1-Leitlinie, die Erläuterung der klinischen Relevanz der Klassifikation EAES 2015, die wissenschaftliche Begründung der wichtigsten Empfehlungen und die Darstellung stadiengerechter Therapieoptionen.

Dr. med. Mihailo Andric
Berufsverband der Deutschen Chirurgie e.V.