Deriving new sources of hepatocytes is critical for further advancement of liver-directed cell therapies, bioartificial liver-assist devices and toxicology studies. The need for new sources of hepatocytes stems from the overall shortage of human hepatocytes, suboptimal condition of human cells available for experiments and potential hazards associated with employing xenogenic (murine or porcine) liver cells. An ideal source of hepatocytes should be capable of population expansion;therefore, emphasis is being placed on investigating progenitor cells or human embryonic stem cells (hESC), cells that could first be expanded and then induced to express liver-specific function. However, success in driving hESC toward hepatic lineage has been limited so far, with attempts to induce liver-specific differentiation in vitro leading to only a small percentage of stem cells expressing such liver-specific markers as albumin and 11-antitrypsin. Traditional cell culture approaches employed in stem cell differentiation studies vary biological inducers one-at-a-time, requiring large numbers of cells and considerable time investment for thorough analysis. In addition, these culture techniques are not well-suited for engineering the precise composition of the microenvironment (e.g. intercellular contacts and cell-surface interactions) required to induce the hepatic phenotype in stem cells. The goal of the present proposal is to design a microenvironment niche conducive to in vitro differentiation of stem cells toward the liver phenotype. In order to converge on the composition of liver-specific stem cell niche, we propose to develop microfabricated cell culture surfaces where the interactions of hESC with extracellular matrix (ECM) proteins, growth factors and other cells (e.g. adult hepatocytes or nonparenchymal liver cells) will be precisely defined and tested in both rational and "combinatorial" fashion. In addition, we will develop growth factor- containing scaffolds as a way of bridging in vitro hESC differentiation studies and stem cell transplantation experiments. Stem cell-carrying heparin hydrogel microstructures will be implanted in immunodeficient mice and survival/function of cells within these constructs will be characterized. Successful completion of this proposal will lead to better understanding of the exogenous cues required for the liver-specific differentiation of hESC, improved efficiency in driving stem cells towards the hepatic phenotype and development of novel biomimetic scaffolds for stem cell transplantation. Overall, the proposed project will enable future applications of hESCs in the development of liver-related therapies.

Public Health Relevance

The liver is an important organ because it removes wastes from the body and plays a significant role in metabolism. Therefore, inherited or acquired liver disorders represent a major health problem. Currently, the only established successful treatment for end-stage liver disease is liver transplantation. However, the number of donor livers is severely inadequate and a large fraction of patients with liver failure do not receive a donor organ. Therefore, it will be greatly beneficial for scientists to identify a cell source that could create an unlimited supply of functional human liver cells. These cells would have the potential to be applied in liver-assist devices or to be transplanted into a patient. Embryonic stem cells (ESC) do not age and have the potential to become most cell types. However, success in driving ESC toward becoming liver cells has been limited so far and only a small percentage of stem cells can be directed to become functional liver cells. We propose to develop novel cell culture tools to precisely control the environment directly surrounding the ESCs or stem cell "niche" that will encourage them to become functional liver cells. Because our platform will be miniature in scale, we will be able to complete many experiments at once to define an optimal liver-specific microenvironment without needing an abundance of cells or proteins.

Agency
National Institute of Health (NIH)
Institute
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
Type
Research Project (R01)
Project #
5R01DK079977-03
Application #
8247791
Study Section
Bioengineering, Technology and Surgical Sciences Study Section (BTSS)
Program Officer
Serrano, Jose
Project Start
2010-05-01
Project End
2015-03-31
Budget Start
2012-04-01
Budget End
2013-03-31
Support Year
3
Fiscal Year
2012
Total Cost
$353,680
Indirect Cost
$103,408
Name
University of California Davis
Department
Biomedical Engineering
Type
Schools of Engineering
DUNS #
047120084
City
Davis
State
CA
Country
United States
Zip Code
95618
Patel, Dipali; Haque, Amranul; Jones, Caroline N et al. (2014) Local control of hepatic phenotype with growth factor-encoded surfaces. Integr Biol (Camb) 6:44-52
Gao, Wei; Zhou, Ping; Ma, Xiaocui et al. (2014) Ethanol negatively regulates hepatic differentiation of hESC by inhibition of the MAPK/ERK signaling pathway in vitro. PLoS One 9:e112698
Shah, Sunny S; Kim, Mihye; Foster, Elena et al. (2012) Electrochemical release of hepatocyte-on-hydrogel microstructures from ITO substrates. Anal Bioanal Chem 402:1847-56
Seo, Jeong Hyun; Chen, Li-Jung; Verkhoturov, Stanislav V et al. (2011) The use of glass substrates with bi-functional silanes for designing micropatterned cell-secreted cytokine immunoassays. Biomaterials 32:5478-88
Ghaedi, Mahboobe; Tuleuova, Nazgul; Zern, Mark A et al. (2011) Bottom-up signaling from HGF-containing surfaces promotes hepatic differentiation of mesenchymal stem cells. Biochem Biophys Res Commun 407:295-300
Tuleuova, Nazgul; Lee, Ji Youn; Lee, Jennifer et al. (2010) Using growth factor arrays and micropatterned co-cultures to induce hepatic differentiation of embryonic stem cells. Biomaterials 31:9221-31