Literature DB >> 16726889

Influence of feeder layer type on the efficiency of isolation of porcine embryo-derived cell lines.

J A Piedrahita1, G B Anderson, R H Bondurant.   

Abstract

Experiments were conducted to determine the effects of feeder layers composed of different cell types on the efficiency of isolation and the behavior of porcine embryo-derived cell lines. Inner cell masses (ICM) isolated from 7- to 8-d-old embryos were plated on feeder layers composed of Buffalo rat liver cells (BRL), a continuous cell line of murine embryonic fibroblasts (STO), STO combined with BRL at a 9:1 and 1:1 ratio, STO with BRL-conditioned medium (STO + CM), porcine embryonic fibroblasts (PEF), PEF combined with BRL at a 9:1 and 1:1 ratio, porcine uterine epithelial cells (PUE), murine embryonic fibroblasts (MEF), or an epithelial-like porcine embryo-derived cell line (PH3A). It was found that embryo-derived cell lines could be isolated only from the STO and the STO with BRL-conditioned medium treatments. The isolated cell lines were of epithelial-like and embryonic stem cell-like (ES-like) morphology. The feeders tested had an effect on the behavior of plated ICM. Some feeders, represented by PUE, BRL, STO:BRL (1:1), PEF:BRL (1:1), and PH3A, did not promote attachment of the ICM to the feeder layer; others, represented by STO and MEF, allowed attachment, differentiation and proliferation. On PEF feeders the ICM spread onto the feeder layer after attachment without apparent signs of proliferation or differentiation. None of the feeders tested increased the efficiency of isolation or the growth characteristics of embryo-derived (both ES-like and epithelial-like) cell lines over that of STO feeders.

Entities:  

Year:  1990        PMID: 16726889     DOI: 10.1016/0093-691x(90)90558-b

Source DB:  PubMed          Journal:  Theriogenology        ISSN: 0093-691X            Impact factor:   2.740


  16 in total

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Authors:  Neil C Talbot; Le Ann Blomberg
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Review 2.  Porcine embryonic stem cells: a possible source for cell replacement therapy.

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Journal:  Stem Cell Rev       Date:  2008-12       Impact factor: 5.739

3.  Derivation of buffalo embryonic stem-like cells from in vitro-produced blastocysts on homologous and heterologous feeder cells.

Authors:  Dharmendra Kumar; T Anand; K P Singh; M K Singh; R A Shah; M S Chauhan; P Palta; S K Singla; R S Manik
Journal:  J Assist Reprod Genet       Date:  2011-05-04       Impact factor: 3.412

4.  Reprogramming of pig dermal fibroblast into insulin secreting cells by a brief exposure to 5-aza-cytidine.

Authors:  G Pennarossa; S Maffei; M Campagnol; M M Rahman; T A L Brevini; F Gandolfi
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5.  Studies on the establishment of a co-culture system of lung stage Schistosoma japonicum with host cells.

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6.  Culture conditions and signalling networks promoting the establishment of cell lines from parthenogenetic and biparental pig embryos.

Authors:  Tiziana A L Brevini; Georgia Pennarossa; Laura Attanasio; Arianna Vanelli; Bianca Gasparrini; Fulvio Gandolfi
Journal:  Stem Cell Rev Rep       Date:  2010-09       Impact factor: 5.739

7.  The effects of human leukemia inhibitory factor (hLIF) and culture medium on in vitro differentiation of cultured porcine inner cell mass (pICM).

Authors:  K Moore; J A Piedrahita
Journal:  In Vitro Cell Dev Biol Anim       Date:  1997-01       Impact factor: 2.416

8.  Bovine embryonic stem cell-like cell lines cultured over several passages.

Authors:  S Saito; N Strelchenko; H Niemann
Journal:  Rouxs Arch Dev Biol       Date:  1992-05

Review 9.  The promise of stem cell research in pigs and other ungulate species.

Authors:  Bhanu Prakash V L Telugu; Toshihiko Ezashi; R Michael Roberts
Journal:  Stem Cell Rev Rep       Date:  2010-03       Impact factor: 5.739

10.  Production of calves by transfer of nuclei from cultured inner cell mass cells.

Authors:  M Sims; N L First
Journal:  Proc Natl Acad Sci U S A       Date:  1994-06-21       Impact factor: 11.205

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