Literature DB >> 23397443

A feeder-cell independent subpopulation of the PICM-19 pig liver stem cell line capable of long-term growth and extensive expansion.

Neil C Talbot1, Thomas J Caperna.   

Abstract

A method for the feeder-independent culture of PICM-19 pig liver stem cell line was recently devised, but the cell line's growth was finite and the cells essentially ceased dividing after approximately 20 passages over a 1 year culture period. Here we report the isolation, continuous culture, and initial characterization of a spontaneously arising feeder-independent PICM-19 subpopulation, PICM-19FF, that maintained replication rate and hepatocyte functions over an extended culture period. PICM-19FF cells grew to 90-98 % confluency after each passage at 2 week intervals, and the cells maintained a high cell density after 2 years and 48 passages in culture (average of 2.6 × 10(6) cells/T25 flask or 1 × 10(5) cells/cm(2)). Morphologically, the PICM-FF cells closely resembled the finite feeder-independent PICM-19 cultures previously reported, and, as before, no spontaneous formation of 3D multicellular ductules occurred in the cells' monolayer. Their bipotent stem cell nature was therefore not evident. Over extensive passage, cytochrome P450 (EROD) activity was maintained, although urea production was reduced on a per mg protein basis at later passages. Two other attributes of fetal hepatocytes, γ-glutamyl transpeptidase activity and serum-protein secretion, were also shown to be maintained by the PICM-19FF cells. The PICM-19FF cells therefore appear to have indefinite growth potential as a feeder-independent cell line and this should enhance the experimental usefulness of the cell line, in general, and may also improve its application to toxicological/pharmacological assays and artificial liver devices.

Entities:  

Year:  2013        PMID: 23397443      PMCID: PMC3886535          DOI: 10.1007/s10616-013-9541-y

Source DB:  PubMed          Journal:  Cytotechnology        ISSN: 0920-9069            Impact factor:   2.058


  13 in total

1.  Characterization of two subpopulations of the PICM-19 porcine liver stem cell line for use in cell-based extracorporeal liver assistance devices.

Authors:  Neil C Talbot; Thomas J Caperna; Ryan R Willard; John H Meekin; Wesley M Garrett
Journal:  Int J Artif Organs       Date:  2010-06       Impact factor: 1.595

2.  Feeder-independent continuous culture of the PICM-19 pig liver stem cell line.

Authors:  Neil C Talbot; Le Ann Blomberg; Wesley M Garrett; Thomas J Caperna
Journal:  In Vitro Cell Dev Biol Anim       Date:  2010-07-07       Impact factor: 2.416

3.  Ultrastructure, enzymatic, and transport properties of the PICM-19 bipotent liver cell line.

Authors:  N C Talbot; T J Caperna; L T Lebow; D Moscioni; V G Pursel; C E Rexroad
Journal:  Exp Cell Res       Date:  1996-05-25       Impact factor: 3.905

4.  Selective and organotypic culture of intrahepatic bile duct cells from adult pig liver.

Authors:  N C Talbot; T J Caperna
Journal:  In Vitro Cell Dev Biol Anim       Date:  1998 Nov-Dec       Impact factor: 2.416

5.  Culture of porcine hepatocytes or bile duct epithelial cells by inductive serum-free media.

Authors:  Thomas J Caperna; Le Ann Blomberg; Wesley M Garrett; Neil C Talbot
Journal:  In Vitro Cell Dev Biol Anim       Date:  2011-02-07       Impact factor: 2.416

6.  Histochemical and ultrastructural demonstration of gamma-glutamyl transpeptidase activity.

Authors:  A M Rutenburg; H Kim; J W Fischbein; J S Hanker; H L Wasserkrug; A M Seligman
Journal:  J Histochem Cytochem       Date:  1969-08       Impact factor: 2.479

Review 7.  Ammonia toxicity and its prevention in inherited defects of the urea cycle.

Authors:  V Walker
Journal:  Diabetes Obes Metab       Date:  2009-06-16       Impact factor: 6.577

8.  The PICM-19 cell line as an in vitro model of liver bile ductules: effects of cAMP inducers, biopeptides and pH.

Authors:  Neil C Talbot; Thomas J Caperna; Kevin D Wells
Journal:  Cells Tissues Organs       Date:  2002       Impact factor: 2.481

9.  A continuous culture of pluripotent fetal hepatocytes derived from the 8-day epiblast of the pig.

Authors:  N C Talbot; C E Rexroad; A M Powell; V G Pursel; T J Caperna; S L Ogg; N D Nel
Journal:  In Vitro Cell Dev Biol Anim       Date:  1994-12       Impact factor: 2.416

10.  Colony isolation and secondary culture of fetal porcine hepatocytes on STO feeder cells.

Authors:  N C Talbot; V G Pursel; C E Rexroad; T J Caperna; A M Powell; R T Stone
Journal:  In Vitro Cell Dev Biol Anim       Date:  1994-12       Impact factor: 2.416

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  3 in total

Review 1.  Stages based molecular mechanisms for generating cholangiocytes from liver stem/progenitor cells.

Authors:  Wei-Hui Liu; Li-Na Ren; Tao Chen; Li-Ye Liu; Li-Jun Tang
Journal:  World J Gastroenterol       Date:  2013-11-07       Impact factor: 5.742

2.  Magnetic cell labeling of primary and stem cell-derived pig hepatocytes for MRI-based cell tracking of hepatocyte transplantation.

Authors:  Dwayne R Roach; Wesley M Garrett; Glenn Welch; Thomas J Caperna; Neil C Talbot; Erik M Shapiro
Journal:  PLoS One       Date:  2015-04-09       Impact factor: 3.240

Review 3.  Unbalanced distribution of materials: the art of giving rise to hepatocytes from liver stem/progenitor cells.

Authors:  Wei-Hui Liu; Li-Na Ren; Tao Chen; Nan You; Li-Ye Liu; Tao Wang; Hong-Tao Yan; Hao Luo; Li-Jun Tang
Journal:  J Cell Mol Med       Date:  2013-11-28       Impact factor: 5.310

  3 in total

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