Current Transplantation Reports

, Volume 2, Issue 2, pp 202–210 | Cite as

New Tools in Experimental Cellular Therapy for the Treatment of Liver Diseases

  • Jennifer R. Ferrer
  • Attasit Chokechanachaisakul
  • Jason A. Wertheim
Cellular Transplants (A Pileggi, Section Editor)
Part of the following topical collections:
  1. Topical Collection on Cellular Transplants

Abstract

The current standard of care for end stage liver disease is orthotopic liver transplantation (OLT). Through improvement in surgical techniques, immunosuppression, and general medical care, liver transplantation has become an effective treatment over the course of the last half-century. Unfortunately, due to the limited availability of donor organs, there is a finite limit to the number of patients who will benefit from this therapy. This review will discuss current research in experimental cellular therapies for acute, chronic, and metabolic liver failure that may be appropriate when liver transplantation is not an immediate option.

Keywords

Hepatocyte transplantation Cellular therapy Alternative cell sources Stem cells 

Introduction

A healthy liver is remarkable in its intrinsic ability to regenerate and heal itself in response to a wide range of injurious stimuli. However, when liver health is compromised by viral infection, metabolic deficiency, genetic abnormality, or alcohol abuse, the regenerative capacity of the liver is diminished. For many people worldwide, this leads to development of acute liver disease (ALD), metabolic liver disease or chronic liver disease leading to end-stage liver disease (ESLD). For a patient with ESLD of any etiology, the standard of care for over 30 years has been orthotopic liver transplantation (OLT), either deceased donor liver transplant (DDLT) or living donor liver transplant (LDLT). OLT is the only curative means of treating ALD, chronic liver disease, and inborn metabolic disease by effectively replacing the failing liver with a healthy liver graft. However, the number of available liver donors limits this life-saving surgical procedure. Despite improvements in surgical technique, such as split-liver and living-related liver donor grafts, and efforts to increase the donor pool by broadening donor criteria, the number of organ transplants performed annually has remained stagnant over the last 10 years while the number of patients in need of a liver transplant continues to grow. Therefore, alternatives to liver transplantation must be considered and further developed.

Hepatocyte transplantation (HT) is one such alternative that focuses on reconstituting the liver parenchyma as opposed to outright replacing it. HT requires the isolation of human hepatocytes from livers unsuitable for OLT and subsequent transplantation of cells into patients with liver disease via portal vein injection or injection into the spleen [1, 2, 3]. Due to the high number of cells needed to achieve a therapeutic effect and high risk of portal vein thrombosis, HT generally requires multiple infusions of donor cells [4, 5]. Nonetheless, this approach is far less invasive than OLT and bypasses many of the complications associated with such an invasive surgery, such as risk of infection, biliary stricture/leak, excessive bleeding, and cardiac injury. This makes hepatocyte transplantation a potentially safer alternative, especially for high-risk patients. To date, at least 100 patients have successfully received a hepatocyte transplant worldwide [6, 7, 8]. HT is mainly used to correct enzyme deficiencies in children with inborn metabolic disease, which is a small component of liver diseases that necessitate OLT (Table 1). HT can reverse hepatic failure in acute liver disease; however, only partial correction of metabolic dysfunction is often achieved, and treating chronic liver disease with HT has not demonstrated significant success due to the more complicated nature of ESLD [10]. Numerous clinical trials validated the long-term safety of HT [11, 12, 13, 14]. However, there remains several limitations that prevent HT from becoming a widely used therapy, despite its advantage as a less invasive and potentially safer alternative to OLT. The major limitations associated with HT are the short lifespan of isolated hepatocytes, low engraftment efficiency, variable hepatocyte quality, and an inability to expand primary hepatocytes ex vivo.
Table 1

Summary of primary cause of liver disease treated by liver transplantation

Primary cause of disease

Percentage

Hepatitis C virus (HCV)

24.5

Malignancy

22.4

Alcoholic liver disease

17.2

Cholestatic disease

8

Acute hepatic necrosis

3.7

Metabolic liver disease

2.4

Other

22

Table adapted from [9]

Barriers to Successful Primary Hepatocyte Transplantation

HT generally requires multiple infusions to achieve therapeutic efficacy. However, cold storage of hepatocytes requires optimal conditions to maintain high numbers of viable, minimally damaged cells diminishing the ability to bank cells for transplantation. The standard storage condition for freshly isolated hepatocytes is below 4 °C. At this temperature, metabolism slows, but cellular damage remains inevitable. Gramignoli et al. showed that immediately following isolation, cell viability is ∼80 %. After 24 h in cold storage, viability drops to 60 % and after 72 h, less than 50 % of cells remain viable [15]. Although cell viability decreased over time, functionality appeared normal, as measured by ability to attach to an extracellular matrix cell culture substrate, metabolize ammonia, and express the CYP 1A, 3A, and 2C family of P450 enzymes. Freshly isolated hepatocytes can be cryopreserved for later use; however, cryopreservation leads to lower engraftment efficiency compared to fresh hepatocytes. Therefore, development of methods using new storage solutions and conditions to improve cold storage of hepatocytes need to be further explored and validated [16].

Engraftment efficiency is a difficult marker to assess and can only be gauged in retrospect. Roll et al. demonstrated that injection of nonviable human hepatocytes into mice led to detection of human albumin in mouse serum that remained detectable for over a week [17]. These results confound standard analysis of engraftment efficiency, as albumin production is often used as a marker of hepatocyte graft function. Other factors that may influence engraftment include duration after cell isolation, number of transplanted donor cells, health and viability of donor cells, and donor–recipient matching and compatibility. Although animal models used to assess human hepatocyte transplantation strategies are useful, many may not truly represent the engraftment process in humans [18]. Methods to improve cell engraftment, such as liver preconditioning, hepatic irradiation, and portal embolization, have been successful in animal models and are being validated for human application [19, 20, 21]. Extra-hepatic implantation sites, such as the spleen, have also been investigated as engraftment sites and many studies demonstrated that injected hepatocytes home to and colonize the spleen [22, 23•]. Often times, the ectopic transplantation site is capable of compensating for primary liver failure, but the frequency depends on the number of transplanted cells that eventually engraft into the ectopic site.

The major hurdle to successful HT is isolation of sufficient quantity of cells with high potency. For some cases of metabolic liver disease, replacing less than 10 % of the liver volume with transplanted hepatocytes may lead to a degree of clinical benefit [4, 6]. For most cases, however, at least 20–30 % of the liver volume will need to be augmented by transplanted hepatocytes [24]. Nonetheless, primary adult hepatocyte transplantation has a known benefit [8]. When compared with fetal hepatocytes and embryonic stem cell-derived endodermal cells in an ALD mouse model, adult hepatocytes had the highest survival rate and proliferative capacity at 35 days post transplantation [25]. It is possible to increase donor cell number by mixing hepatocytes isolated from livers removed during OLT for metabolic disease. Hepatocytes from these livers, aside from a deficiency in a single enzyme, are functional hepatocytes. In comparison to hepatocytes isolated from a healthy donor liver, hepatocytes from metabolic diseased livers demonstrate similar cell viability, plating efficiency, morphology, and performance in assays of liver function, such as ammonia metabolism, drug metabolism, and conjugation reactions [26]. Additionally, hepatocytes with a metabolic deficiency were able to repopulate an FRG mouse liver with 50–99 % efficiency and produced human albumin. Primary hepatocytes can also be modified to induce immortality thus allowing ex vivo expansion. Meng et al. isolated primary human hepatocytes and transduced them with a retroviral vector containing SV40T and a hygromycin resistant gene. Though SV40T induced immortality, there remain concerns over the use of viral vectors in the clinical setting due to possible expression of viral genes in transfected cells. To address this concern, the SV40T gene cDNA was excised using Cre/loxP site-specific recombination in isolated, expanded clones [27]. This method makes it possible to expand human hepatocytes ex vivo and remove their proliferative capacity before transplantation.

Although primary human hepatocytes have demonstrated clinical safety and success in a limited number of cases, the aforementioned limitations prevent their widespread use as a therapy. Hepatocyte transplantation requires large numbers of donor cells in order to be effective. Alternative cell sources, namely stem and progenitor cells, are now being investigated and address issues of expansion, variable donor quality, the requirement of immunosuppression, and longevity.

Alternative Cell Sources for Hepatocyte Transplantation

Liver Stem/Progenitor Cells

Liver progenitor cells, also called hepatic oval cells, are bipotential cells that are activated and expand in the liver parenchyma when mature hepatocytes are exposed to liver injury, thus playing a major role in liver repair and regeneration (Fig. 1). These cells are present in low numbers in a healthy liver, but are capable of differentiating into either hepatocytes or biliary cells and compensate for liver function when hepatocytes and biliary cells are impaired [28, 29]. These cells are a potential experimental cell source for HT because liver progenitor cells can be isolated and stimulated ex vivo to differentiate into mature hepatocytes [30, 31]. Alternatively, progenitor cells can be recovered from livers with chronic liver injury and potentially expanded ex vivo for cell therapy applications. Using a mouse model of oval cell activation, Tarlow et al. discovered that both human and mouse hepatocytes undergo a sort of dedifferentiation to a progenitor state that can then be reversed [32•]. However, alternative models of hepatocyte proliferation in response to injury leading to liver regeneration have been recently proposed and suggest that mature hepatocytes participate in the repair process [33, 34].
Fig. 1

Description of cell sources that have been investigated for use in hepatocyte transplantation

Mesenchymal Stem Cells

Mesenchymal stem cells (MSCs) are of extra-hepatic origin and are adherent, fibroblast-like non-hematopoietic progenitor cells. MSCs are a population of stem cells that are being explored experimentally for regenerative purposes due to their multipotency. Most research involves the use of bone marrow-derived MSCs (BM-MSCs), but MSCs can be retrieved from other tissues and organs, including the umbilical cord and subcutaneous adipose tissue [35, 36, 37, 38]. Recent evidence suggests that MSCs are capable of sensing injury and such signals promote MSC migration to injury sites and facilitate repair or regeneration. There is overlap between the ability of liver stem cells and BM-MSCs to induce liver regeneration [39, 40]. The use of MSCs as a cellular therapy for liver disease has been demonstrated in both animal models and in limited clinical studies. In one study, human umbilical cord blood-derived MSCs (hUCBMSs) were transplanted via tail vein injection into SCID mice with d-galactoasmine/LPS induced liver injury. hUCBMSCs differentiated into hepatocyte-like cells that homed to the liver and attenuated liver damage, as assessed by H&E, which demonstrated resolution of liver damage, disappearance of inflammatory cell infiltration, and decreased necrosis [41]. In a clinical setting, 40 patients with hepatitis C were divided into two groups, with one group receiving BM-MSCs either by intrasplenic or intrahepatic transplantation, while the other group received traditional supportive treatment for Hepatitis C virus. The results of this study, which followed patients for 6 months, showed improvement in MELD scores, Child-Pugh scores, and serum albumin levels in patients that received the MSC transplant, suggesting that BM-MSCs may be safe and effective for the treatment of liver failure [42].

Induced Pluripotent Stem Cells

Induced pluripotent stem (iPS) cells are derived from terminally differentiated cells, such as skin fibroblasts, and are made pluripotent by expression of specific transcription factors [43]. These cells represent a potentially ideal source of hepatocytes for transplantation in that these cells can be generated in a patient-specific manner, potentially negating the need for immunosuppression. iPS-derived hepatocytes (iPS-heps) have been generated from a range of somatic cells from various donors, and any variation in differentiated iPS-heps, interestingly, can be attributed to donor differences rather than the initial cell type used, suggesting that iPS-heps may be a more homogenous population of cells than freshly isolated hepatocytes [44, 45]. A number of studies have tested the efficacy of liver repopulation using human iPS-derived hepatocytes in mouse models. In one study, wild-type iPS cells were injected into fumarylacetoacetate hydrolase (FAH) knockout mouse blastocysts. FAH −/− mice lack the fumaryl-acetoacetate hydrolase enzyme, and this deficiency is a model for tyrosinemia type I [46]. These mice consistently develop liver disease when a protective drug that prevents tyrosine degradation, 2-(2-nitro-4-trifluoromethylbenzoyl)-1,3-cyclohexanedione (NTBC), is withdrawn. The FAH −/− blastocysts complemented with wild-type iPS cells were then transferred into foster mothers, and chimeric neonates showed growth and survival even when NTBC was withdrawn, suggesting hepatocytes derived from FAH +/+ iPS cells were functional and could compensate for the liver disease that is lethal to neonates [47]. In another study, rather than generate true iPS cells, the authors transformed human fibroblasts into multipotent progenitor cells from which hepatocyte-like cells could be generated. These induced multipotent progenitor-heps, unlike iPS-heps, proliferated extensively and demonstrated hepatocyte function similar to human adult hepatocytes when transplanted into an immune-deficient mouse model of human liver failure [48•]. These results are particularly impressive, and suggest that a large number of patient-specific hepatocyte-like cells can be generated in vitro. One limitation to this strategy, and other protocols developing iPS cells and iPS-heps, is the time scale required to generate mature hepatocytes and their limited functionality compared to primary human hepatocytes. In general, it takes at least 3 weeks to generate iPS cells and differentiate them toward a hepatocyte-like lineage [45, 49, 50]. However, Tomizawa et al. developed a protocol to differentiate iPS cells into iPS-heps in eight days. iPS cells were exposed to a combination of oncostatin M, epidermal growth factor, retinoic acid, dexamethasone, and ITS, supplemented with various growth factors. iPS cells were hepatocyte-like in their expression of GATA4, GATA6, Sox17, FoxA2, HNF4a, but did not produce albumin [51]. As albumin production is a hallmark of hepatocyte function, this strategy, though more expedient than other protocols, requires additional investigation.

Other Cell Sources

Other cell sources that have been explored as potential cellular therapies for liver disease include embryonic stem cells, a human hepatoma cell line, xenogeneic hepatocytes, and humanized mouse hepatocytes [52, 53, 54, 55, 56, 57, 58]. These cell types will not be described in detail in this review, however, it should be noted that xenogeneic tissue and humanized animal hepatocytes have the greatest potential to address the donor limitation of primary human hepatocytes, but issues regarding tissue matching and zoonosis remain.

Hepatocyte Transplantation into Animal Models of Liver Disease

In order to gauge the efficacy of hepatocytes and other cell sources for transplantation, animal models that accurately recapitulate human liver diseases are desperately needed. Small rodents, especially mice, are an attractive animal model because of their ease of handling, short life span, and broad genetic similarity. The development of numerous animal models of liver disease has led to a new understanding of the mechanism of liver repair and regeneration in recent years.

Metabolic Liver Disease

Although HT is not yet a widely used therapy, it has been most successful in treatment of inborn metabolic disorders. There are several animal models of metabolic liver disease, including the Gunn rat model of Crigler-Najjar syndrome, the Watanabe rabbit for familial hypercholesterolemia, and the FAH models of hereditary tyrosinemia [59, 60, 61, 62, 63••]. Crigler-Najjar syndrome is an autosomal recessive disorder that is characterized by low expression or absence of the enzyme uridine diphosphate glucuronosyltransferase. This mutation prevents patients with Crigler-Najjar syndrome from completely metabolizing bilirubin, resulting in jaundice and potential brain damage. The Gunn rat lacks the uridine diphosphate glucuronosyltransferase enzyme, is also jaundiced, and has been used for decades to study Crigler-Najjar syndrome. Recently, Maerckx et al. showed that transplantation of differentiated human liver progenitor cells into the Gunn rat corrects for the enzyme deficiency and lowers serum bilirubin levels [64]. In their study, hepatocytes isolated from a healthy male donor post-mortem expanded and differentiated ex vivo into mature hepatocyte-like cells with CYP3A4 activity. These cells were injected into the portal vein of Gunn rats, and serum bilirubin levels were assessed at multiple time points. Compared with rats that received a transplantation of cryopreserved hepatocytes, rats that received the differentiated progenitor cells had a similar reduction in serum bilirubin over a period of 27 weeks. Although HT has already been used to successfully treat patients with Crigler-Najjar syndrome, the Gunn rat remains a valuable tool for developing and optimizing strategies for HT as well as for testing the performance of alternative cell sources.

Hereditary tyrosinemia is an autosomal recessive disease that is caused by a deficiency in the FAH enzyme, which catalyzes the last step of tyrosine metabolism. This deficiency results in buildup of toxic metabolic byproducts that may lead to death if left untreated. The FAH knockout mouse is an excellent tool for studying hereditary tyrosinemia and for developing cellular therapies for this disease. In this model, both allogeneic BM-MSC and xenogeneic hepatocyte transplantation can successfully repopulate the mouse liver and rescue the enzyme deficiency (Fig. 2) [66, 67]. More recently, hepatic progenitor-like cells have been used as a cell source for HT into this animal model. In one study, mouse embryonic fibroblasts were reverted to a hepatic progenitor state by the transduction of two liver liver-specific transcription factors, HNF1β and Foxa3, important for liver organogenesis. When these cells were cultured in vitro on different substrates, they differentiated into both hepatocytes and cholangiocytes. When the stem cells were transplanted into the spleen of FAH knockout mice, they populated the liver and differentiated into hepatocytes and restored liver function [68]. In another study, fetal fibroblasts were isolated from pregnant FAH knockout mice and reprogrammed into iPS cells by transducing Oct4, Sox2, Klf4, and c-Myc transcription factors. The FAH mutation was corrected in these iPS cells by transfecting the cells with a viral vector expressing wild-type FAH cDNA. The genetically corrected cells were complemented with tetraploid embryos and transferred into pseudopregnant FAH knockout mothers. Almost 25 % of complemented embryos developed into viable pups [69]. The results from both of these studies are promising and exciting because iPS cells can be derived in a patient-specific manner, possibly bypassing the need for immunosuppressants. Even patients with metabolic disease can potentially benefit from self-derived iPS cells if gene correction can be done efficiently. However, testing the efficacy of gene correction of human iPS cells poses a limitation, as tetraploid embryo complementation cannot be tested in humans.
Fig. 2

Isolation of primary human hepatocytes and implantation into a FAH −/− recipient allows for repopulation and restoration of liver function. (Reproduced with permission from [65]

There are additional animal models of inborn metabolic liver diseases that have been successfully treated by HT [70, 71, 72, 73, 74]. Unlike models of acute and chronic liver disease, it is easier to recapitulate the etiology and presentation of metabolic liver disease in animals because the disease is caused by a gene mutation resulting in deficiency of a single enzyme. The FAH knockout pig by Hickey et al. is an especially important development because there are few large animal models of liver disease, and large animal models provide another layer of therapy validation in advance of human studies [63••]. The development and use of these models to validate HT has and will continue to be critical to its translation into the clinic.

Acute Liver Disease

Acute liver failure (ALF) is a severe liver disease with rapid onset and very high mortality. Only about 40 % of patients with fulminant liver failure can be treated with medical management, and in those cases, it is the regenerative ability of the liver that allows the organ to recover, avoiding the need for OLT. A barrier to treating ALF with HT is that patients require transplantation of healthy hepatocytes that function immediately to correct liver failure [75]. For this reason, Sun et al. asserts that BM-MSCs are an appropriate choice for HT [76]. In a Concanavalin A-induced mouse model of ALF, Sun et al. found that only BM-MSC injection into the spleen (and not adult hepatocytes, induced hepatocytes or fetal liver cells) were capable of partially rescuing animals with liver failure, as observed by a reduction in the inflammatory response and overall prolonged survival. However, the efficacy of a cell-based therapy seems to vary with the choice of animal model. In one study that used diphtheria toxin to induce ALF in mice, transplanted adult hepatocytes showed higher engraftment and survival rates as well as proliferation when compared to fetal liver cells and ESC-derived endodermal cells while yet another model of ALF (using LPS and D-galactosamine in rats) found that BM-MSCs homed to the liver and improved liver function [25, 77].

Another animal model, the Long-Evans Cinnamon (LEC) rat, spontaneously develops fulminant hepatitis during old age (80–120 days), and acute hepatic failure occurs due to copper accumulation from incomplete deletion of the copper transporter gene (Atp7b). This model more closely relates to Wilson’s Disease, an autosomal recessive genetic disorder characterized by a disruption of copper metabolism leading to copper accumulation in the liver. But in the context of ALF, one study used LEC rats fed with a high-copper diet to rapidly induce liver failure. These animals were transplanted with Long-Evans agouti rat wild-type hepatocytes. Even in the presence of continued oral intake of copper in the diet, multiple rounds of infusions of adult hepatocytes into the spleen were required to delay onset of hepatitis (40 % rats), normalize hepatitis-associated serum markers and prolong survival until the end of the study, while rats with one or no infusion of hepatocytes failed to survive past 22 days [78].

There are a variety of animal models that mimic the onset and symptoms of ALF that are induced surgically, pharmacologically, or through a combination of each [79, 80]. Perhaps the most promising application of BM-MSCs has been the work of Li et al. in which a porcine model of ALF was used [81•]. While small animal models are useful and can be analyzed quickly with high-throughput, large animal models hold more value in translating potential therapies. In the study by Li et al., ALF was induced by d-galactosamine, and human BM-MSCs were transplanted into pigs via the intra-portal route or peripheral vein injection immediately followed by d-galactosamine administration. Animals that did not receive HT and animals given HT via a peripheral vein died within 96 h. Animals that received intra-portal injection of human MSCs survived longer than 6 months. These results suggest that MSCs immediately begin participating in the regenerative and restorative process to overcome drug-induced ALF. Additionally, treated animals were healthy, suggesting that human BM-MSC transplantation may be safe and effective in a large animal model of ALF and may be promising as a future clinical therapy.

Chronic Liver Disease

Chronic liver disease (CLD) is generally characterized by the presence of inflammation, liver fibrosis, and cirrhosis. Treating chronic liver disease with HT is even more difficult to treat than ALD or inborn metabolic diseases due to the dysregulated architecture of the liver. Excessive extracellular matrix protein accumulation makes HT difficult because blood vessels, like the portal vein, may experience severe hypertension when a bolus of hepatocytes is infused [75]. However, extrahepatic sites, like the spleen and lymph nodes, have the potential to compensate for liver failure if the ectopic sites are colonized or engrafted with sufficient number of cells. Using this strategy, HT in animal models of cirrhosis has shown improvement in liver function, but success in humans has been suboptimal, perhaps due to an insufficient cell load needed to compensate for severely deficient liver function [82, 83, 84]. Like ALF, there are a number of surgical and pharmacological models for CLD, mostly using mice and rats [85, 86]. The most common model uses carbon tetrachloride (CCl4), though thioacetamide and dimethylnitrosamine are often used as well. Though these toxin-induced models do not necessarily replicate the etiology of CLD, they do provide useful tools for assessing the effect of HT on modulating inflammation and fibrosis.

BM-MSCs are an attractive cell source for treating CLD because of their ability to differentiate into hepatocyte-like cells, their regenerative capabilities, and their anti-inflammatory properties. In CCl4-induced mouse models of fibrosis and cirrhosis, undifferentiated and differentiated BM-MSCs engraft in the liver and effectively increase liver function and health, as measured by expression of hepatocyte-specific markers, albumin production, decreased fibrosis and total bilirubin levels. Additionally, BM-MSCs increase the survival rates of CCl4-induced mouse models of liver fibrosis and cirrhosis [87, 88]. Piryaei et al. asserts that in their work, BM-MSCs differentiated into hepatocyte-like cells and functioned better than undifferentiated cells. In an immunodeficient mouse model of non-alcoholic steatohepatitis (NASH), Winkler et al. demonstrated both the regenerative potential of MSCs as well as their anti-inflammatory properties [89]. In this study, the NASH-induced mice showed high levels of α-SMA, a marker of hepatic stellate cell activation, collagen accumulation and high levels of inflammatory markers, like TNFα. But in NASH-induced mice treated with human MSc transplantation, collagen accumulation was decreased as well as α-SMA expression, suggesting reversion of activated stellate cells to a quiescent state and a decrease in their fibrogenic potential. TNFα levels were also reduced, indicating a decrease in inflammation.

NASH is characterized by fat deposition in the liver, fibrosis, and inflammation, and is linked to metabolic syndrome and obesity. Due to the recent development of effective therapies for hepatitis C viral (HCV) infection as well as the steady increase of obesity in the Western world, it is expected that NASH will replace HCV as the most common chronic liver disease and indication for OLT within the next several years. The development of animal models of NASH, which are diet induced, is an important and crucial contribution to understanding the biology of the disease as well as the development of potential therapies [90]. Multiple studies have demonstrated the therapeutic benefit of HT in mouse and rat models of NASH [91, 92, 93]. In each of these studies, HT of either adult hepatocytes or MSCs has led to higher survival rates of animals, lower lipid stores in the liver, and improved liver function.

But perhaps the most promising and exciting development of cell therapy for CLD has been with iPS cells. In work by Liu et al., iPS cells were derived from cells from each of the three developmental germ layers (hepatocytes, fibroblasts, keratinocytes) and differentiated into hepatocyte-like cells. These cells secreted liver-specific proteins with morphology similar to adult hepatocytes. The differentiated hepatocyte-like cells were transplanted into an immunodeficient mouse model with DMN-induced liver fibrosis and were capable of engrafting into the liver (8–15 %) and regenerating the damaged liver regardless of germ layer origin. This is exciting for all the aforementioned benefits of using iPS cells as an alternative cell source for HT, but more specifically because it appears that the epigenetic differences between iPS cells derived from different developmental layers does not affect their ability to differentiate into similarly functional hepatocyte-like cells [94••].

Conclusion

Hepatocyte transplantation research and clinical application has made great strides over recent years. The investigation into various cell sources and the use of animal models of liver disease have provided tools to justify the use of cell-based therapies when whole organ transplantation is not an option. There are still many hurdles to overcome, but increased knowledge and understanding of the liver’s intrinsic ability to regenerate and discoveries harnessing the regenerative potential of hepatocytes and hepatocyte-like cells has the potential to significantly transform the practice of health care and the course of treatment of liver diseases in the near future.

Notes

Acknowledgments

We thank the support of the Zell Family Foundation. J.R.F. acknowledges support from the National Institute of General Medical Sciences of the National Institutes of Health under Award Number T32GM105538. J.A.W. acknowledges support from the Robert R. McCormick Foundation, American Association for the Study of Liver Diseases and the American Liver Foundation’s Liver Scholar Award, Society for Surgery for the Alimentary Tract’s Career Development Award, and NIDDK K08DK10175. This work was supported in part by Health Resources and Services Administration contract 234-2005-37011C. The content is the responsibility of the authors alone and does not necessarily reflect the views or policies of the Department of Health and Human Services, nor does mention of trade names, commercial products, or organizations imply endorsement by the U.S. Government.

Compliance with Ethics Guidelines

Conflict of Interest

Jennifer R. Ferrer and Attasit Chokechanachaisakul declare that they have no conflict of interest.

Jason A. Wertheim reports non-financial support from Cellular Dynamics International, unrelated to the preparation of this manuscript.

Human and Animal Rights and Informed Consent

This article does not contain any studies with human or animal subjects performed by any of the authors.

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Copyright information

© Springer International Publishing AG 2015

Authors and Affiliations

  • Jennifer R. Ferrer
    • 1
    • 2
    • 3
    • 4
    • 5
  • Attasit Chokechanachaisakul
    • 1
    • 6
  • Jason A. Wertheim
    • 1
    • 3
    • 4
    • 5
    • 6
    • 7
    • 8
  1. 1.Department of SurgeryNorthwestern University Feinberg School of MedicineChicagoUSA
  2. 2.Department of ChemistryNorthwestern UniversityEvanstonUSA
  3. 3.Chemistry of Life Processes InstituteNorthwestern UniversityEvanstonUSA
  4. 4.International Institute for NanotechnologyNorthwestern UniversityEvanstonUSA
  5. 5.Simpson Querrey Institute for BioNanotechnology in MedicineNorthwestern UniversityChicagoUSA
  6. 6.Comprehensive Transplant Center, Feinberg School of MedicineNorthwestern UniversityChicagoUSA
  7. 7.Department of SurgeryJesse Brown VA Medical CenterChicagoUSA
  8. 8.Department of Biomedical EngineeringNorthwestern UniversityEvanstonUSA

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