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In This Article

  • Summary
  • Abstract
  • Introduction
  • Protocol
  • Representative Results
  • Discussion
  • Acknowledgements
  • Materials
  • References
  • Reprints and Permissions

Summary

Here we present a non-genetic method to generate human autologous liver spheroids using mononuclear cells isolated from steady-state peripheral blood.

Abstract

Human liver cells can form a three-dimensional (3D) structure capable of growing in culture for some weeks, preserving their functional capacity. Due to their nature to cluster in the culture dishes with low or no adhesive characteristics, they form aggregates of multiple liver cells that are called human liver spheroids. The forming of 3D liver spheroids relies on the natural tendency of hepatic cells to aggregate in the absence of an adhesive substrate. These 3D structures possess better physiological responses than cells, which are closer to an in vivo environment. Using 3D hepatocyte cultures has numerous advantages when compared with classical two-dimensional (2D) cultures, including a more biologically relevant microenvironment, architectural morphology that reassembles natural organs as well as a better prediction regarding disease state and in vivo-like responses to drugs. Various sources can be used to generate spheroids, like primary liver tissue or immortalized cell lines. The 3D liver tissue can also be engineered by using human embryonic stem cells (hESCs) or induced pluripotent stem cells (hiPSCs) to derive hepatocytes. We have obtained human liver spheroids using blood-derived pluripotent stem cells (BD-PSCs) generated from unmanipulated peripheral blood by activation of human membrane-bound GPI-linked protein and differentiated to human hepatocytes. The BD-PSCs-derived human liver cells and human liver spheroids were analyzed by light microscopy and immunophenotyping using human hepatocyte markers.

Introduction

In recent years three-dimensional (3D) spheroid culture systems have become an important tool to study various areas of cancer research, drug discovery, and toxicology. Such cultures raise great interest because they bridge the gap between two-dimensional (2D) cell culture monolayers and complex organs1.

In the absence of an adhesive surface, compared to the 2D cell culture, the formation of spheroids is based on the natural affinity of these cells to cluster in 3D form. These cells organize themselves into groups consisting of one or more types of mature cells. Free of foreign materials, these cells interact with ea....

Protocol

Ethical approval was obtained (ACA CELL Biotech GmbH/25b-5482.2-64-1) for performing these experiments and informed consent was signed by all donors before blood extraction in compliance with institutional guidelines.

1. Preparation of mononuclear cells (MNCs) from human peripheral blood (PB)

  1. Extract 30 mL of blood from healthy donors with the help of trained medical personnel according to the standard protocol.
  2. Isolate PBMNCs using density gradient media.......

Representative Results

We successfully differentiated human BD-PSCs into endoderm/hepatic progenitor cells and hepatocytes by applying a two-step protocol. Morphological changes during the hepatic differentiation process are shown in Figure 1. BD-PSCs differentiate into hepatocytes going through three different stages. The first stage represents the differentiation into endodermal cells L4, the second, differentiation to hepatic progenitor cells (hepatoblast) L8, exhibiting a typical polygonal morphology, and the .......

Discussion

The liver is a major organ in the human body with many essential biological functions, such as the detoxification of metabolites. Due to severe liver failures like cirrhosis and/or viral hepatitis, there are nearly 2 million deaths per year worldwide. Liver transplantations rank second in solid organ transplantations worldwide, but only about 10% of the current need is met22.

Primary human hepatocytes (PHH) are often used to study liver toxicity. These cells can be main.......

Acknowledgements

The authors are especially grateful for the technical assistance provided by Oksana and John Greenacre. This work was supported by ACA CELL Biotech GmbH Heidelberg, Germany.

....

Materials

NameCompanyCatalog NumberComments
Albumin antibodySigma-AldrichSAB3500217produced in chicken
Albumin Fraction VCarl Roth GmbH+Co. KGT8444.4
Alpha-1 FetoproteinProteintech Germany GmbH14550-1-APrabbit polyclonal IgG
Biolaminin 111 LNBioLamina LN111-02human recombinant
CD45 MicroBeadsMiltenyi130-045-801nano-sized magnetic beads
Cell StrainerpluriSelect43-10040-40
CellSens Olympusimaging software
Centrifuge tubes 50 mL Greiner Bio-One210270
CEROplate 96 wellOLS OMNI Life Science2800-109-96
CKX53 Olympus
Commercially available detergentProcter & Gamblenonionic detergent
CYP2E1-specific antibodyProteintech Germany GmbH19937-1-APrabbit polyclonal antibody IgG
CYP3A4 Proteintech Germany GmbH67110-1-lgmouse monoclonal antibody IgG1
Cytokeratin 18DakoCytomationM7010mouse monoclonal antibody IgG1
DMSOSigma-AldrichD8418-50ML
DPBSThermo Fisher Scientific14040091
FBSMerck MilliporeS0115/1030BDiscontinued. Available under: TMS-013-B
Glass cover slips 14 mmR. Langenbrinck01-0014/1
GlutaMax 100x GibcoThermo Fisher Scientific35050038L-glutamine
Glutaraldehyde 25%Sigma-AldrichG588.2-50ML
Goat anti-mouse IgG Cy3Antibodies onlineABIN1673767polyclonal
Goat anti-mouse IgG DyLight 488Antibodies onlineABIN1889284polyclonal
Goat anti-rabbit IgG Alexa Fluor 488Life TechnologiesA-11008
HClSigma-Aldrich30721-1LGL
HepatoZYME-SFM Thermo Fisher Scientific17705021hepatocyte maturation medium
HGFThermo Fisher ScientificPHG0324human recombinant
HNF4α antibodySigma-AldrichZRB1457-25ULclone 4C19 ZooMAb Rbmono
Hydrocortisone 21-hemisuccinate (sodium salt)BiomolCay18226-100
Knock out Serum Replacement - Multi Species GibcoFisher ScientificA3181501KSR
KnockOut DMEM/F-12Thermo Fisher Scientific12660012Discontinued. Available under Catalog No. 10-828-010
MACS BufferMiltenyi130-091-221
MACS MultiStandMiltenyi130-042-303magnetic stand
MEM NEAA 100x GibcoThermo Fisher Scientific11140035
MercaptoethanolThermo Fisher Scientific3135001050mM
MiniMACS columnsMiltenyi130-042-201
Nunclon MultidishesSigma-AldrichD67894 well plates
Oncostatin MThermo Fisher ScientificPHC5015human recombinant
ParaformaldehydeSigma-Aldrich158127
PBS sterileCarl Roth GmbH+Co. KG9143.2
Penicillin/StreptomycinBiochrom GmbHA221310000 U/ml
PS 15ml tubes sterileGreiner Bio-One188171
Rabbit anti-chicken IgG Texas redAntibodies onlineABIN637943
Roti Cell Iscoves MDMCarl Roth GmbH+Co. KG9033.1
Roti Mount FluorCare DAPICarl Roth GmbH+Co. KGHP20.1
Roti Sep 1077 humanCarl Roth GmbH+Co. KG0642.2
Transthyretin antibody Sigma-AldrichSAB3500378produced in chicken
Triton X-100Thermo Fisher ScientificHFH101%

References

  1. Fennema, E., Rivron, N., Rouwkema, J., van Blitterswijk, C., de Boer, J. Spheroid culture as a tool for creating 3D complex tissues. Trends in Biotechnology. 31 (2), 108-115 (2013).
  2. Ryu, N. E., Lee, S. H., Park, H. Sph....

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