DocumentCode
1299252
Title
Hepatocyte growth factor incorporated chitosan nanoparticles differentiate murine bone marrow mesenchymal stem cell into hepatocytes in vitro
Author
Pulavendran, S. ; Rajam, M. ; Rose, C. ; Mandal, A.B.
Author_Institution
Dept. of Biotechnol., Central Leather Res. Inst., Chennai, India
Volume
4
Issue
3
fYear
2010
fDate
9/1/2010 12:00:00 AM
Firstpage
51
Lastpage
60
Abstract
Delivery of growth factor for the differentiation of stem cells into lineage specific cells holds great potential in regenerative medicine. Stem cell differentiation is governed by cytokines and growth factors secreted upon the organelle injury and, however, their short half-life necessitates exogenous supply. Development of suitable nanodevices using biodegradable polymers to deliver therapeutic proteins to the targeted site in a sustainable manner attracts scientists and clinicians. Here, for the first time, hepatocyte growth factor (HGF) was incorporated into chitosan nanoparticles (CNP) by ionotrophic gelation method. An average size of nanoparticles prepared was 100 nm, showing sustainable release of HGF. Cytotoxicity study did not reveal any adverse effect on bone marrow mesenchymal stem cells (MSC) up to 4 mg CNP/ml culture medium. To evaluate the effect of HGF incorporated CNP (HGF-CNP) on hepatic differentiation in in vitro, MSC were incubated with HGF-CNP and other supplements. After 21 days, fibroblast-like morphology of MSC became round-shape, a typical characteristic of hepatocyte cell. Immunofluorescence study for albumin expression confirmed the hepatic differentiation. In conclusion, HGF released from the HGF-CNP can differentiate MSC into hepatocytes, and this novel technique could also be extended to deliver therapeutic proteins for a variety of tissue regeneration.
Keywords
biodegradable materials; biomedical materials; cellular biophysics; nanobiotechnology; nanoparticles; patient treatment; polymers; tissue engineering; HGF incorporated CNP; biodegradable polymers; chitosan nanoparticles; cytokines; cytotoxicity; hepatocyte growth factor; ionotrophic gelation method; lineage specific cells; murine bone marrow mesenchymal stem cell; organelle injury; regenerative medicine; stem cell differentiation; therapeutic protein delivery; tissue regeneration;
fLanguage
English
Journal_Title
Nanobiotechnology, IET
Publisher
iet
ISSN
1751-8741
Type
jour
DOI
10.1049/iet-nbt.2009.0014
Filename
5551074
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