Gene expression and functional analyses of primary rat hepatocytes on nanofiber matrices

Colleen M. Brophy, Jennifer L. Luebke-Wheeler, Bruce P. Amiot, Rory P Remmel, Piero Rinaldo, Scott L. Nyberg

Research output: Contribution to journalArticle

6 Citations (Scopus)

Abstract

Long term culture of primary hepatocytes is valuable for diagnostic and therapeutic applications. However, standard monolayer culture of primary hepatocytes on tissue culture plastic (TCP) - either uncoated or coated with a biological material such as collagen or laminin - is problematic. Thus, novel support matrices are under development to better maintain gene expression and differentiated function of primary hepatocytes in vitro. In this study, a fabricated nanofiber matrix was compared to control conditions of uncoated and laminin-coated TCP. Gene expression and biochemical analyses were performed to compare functional abilities of the hepatocytes in the different conditions. Hepatocytes cultured on nanofibers maintained higher cytochrome P450 1A activity (0.49 ± 0.08 ng resorufin/ml/min) compared to hepatocytes on laminin (0.11 ± 0.05 ng resorufin/ml/min). In addition, albumin production of hepatocytes on nanofibers was greater than twice the production of hepatocytes on laminin (day 14, 34.4 ± 1.8 vs. 15.9 ± 4.5 μg albumin/ml/day). Hepatocytes demonstrated the ability to generate urea from ammonia in all conditions; however, hepatocytes performed ureagenesis more effectively on nanofibers than on laminin (0.55 ± 0.25 μM vs. 0.36 ± 0.24 μM urea, day 14). Gene expression of hepatocytes cultured on nanofiber and laminin conditions were similar on a per cell basis determined by analysis using a custom microarray of 250 genes expressed in hepatocytes. Similar cell attachment data between conditions and similar numbers of cells expressing the hepatocyte marker hepatocyte nuclear factor 4α indicates that hepatocytes grown on nanofibers only marginally display improved hepatic functions compared to laminin control conditions.

Original languageEnglish (US)
Pages (from-to)129-140
Number of pages12
JournalCells Tissues Organs
Volume191
Issue number2
DOIs
StatePublished - Jan 1 2010

Fingerprint

Nanofibers
Hepatocytes
Gene Expression
Laminin
Plastics
Urea
Albumins
Hepatocyte Nuclear Factor 4
Ammonia

Keywords

  • Cell culture
  • Differentiation
  • Extracellular matrix
  • Hepatocytes
  • Liver
  • Tissue engineering

Cite this

Brophy, C. M., Luebke-Wheeler, J. L., Amiot, B. P., Remmel, R. P., Rinaldo, P., & Nyberg, S. L. (2010). Gene expression and functional analyses of primary rat hepatocytes on nanofiber matrices. Cells Tissues Organs, 191(2), 129-140. https://doi.org/10.1159/000223235

Gene expression and functional analyses of primary rat hepatocytes on nanofiber matrices. / Brophy, Colleen M.; Luebke-Wheeler, Jennifer L.; Amiot, Bruce P.; Remmel, Rory P; Rinaldo, Piero; Nyberg, Scott L.

In: Cells Tissues Organs, Vol. 191, No. 2, 01.01.2010, p. 129-140.

Research output: Contribution to journalArticle

Brophy, CM, Luebke-Wheeler, JL, Amiot, BP, Remmel, RP, Rinaldo, P & Nyberg, SL 2010, 'Gene expression and functional analyses of primary rat hepatocytes on nanofiber matrices', Cells Tissues Organs, vol. 191, no. 2, pp. 129-140. https://doi.org/10.1159/000223235
Brophy, Colleen M. ; Luebke-Wheeler, Jennifer L. ; Amiot, Bruce P. ; Remmel, Rory P ; Rinaldo, Piero ; Nyberg, Scott L. / Gene expression and functional analyses of primary rat hepatocytes on nanofiber matrices. In: Cells Tissues Organs. 2010 ; Vol. 191, No. 2. pp. 129-140.
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