Literature DB >> 1906045

Purification of hepatocyte couplets by centrifugal elutriation.

J C Wilton1, D E Williams, A J Strain, R A Parslow, J K Chipman, R Coleman.   

Abstract

An initial preparation of rat hepatocytes containing approximately 30% couplets was enriched by centrifugal elutriation. Of the couplets loaded onto the elutriator, 87% were eluted at medium flow rates of 60 to 80 ml/min at a rotor speed of 1,100 rpm; cells eluted in this range maintained a viability of more than 95%. Peak fractions were enriched in couplets to 84.5% +/- 2.5%. After elutriation, couplets retained the ability to secrete fluorescent cholephiles into sealed canalicular vacuoles. The preparation can now be used in hepatobiliary and hepatotoxicity studies not possible with preparations in which they are minor components.

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Year:  1991        PMID: 1906045     DOI: 10.1002/hep.1840140129

Source DB:  PubMed          Journal:  Hepatology        ISSN: 0270-9139            Impact factor:   17.425


  10 in total

1.  Molecular recognition of peptide and non-peptide ligands by the extracellular domains of neurohypophysial hormone receptors.

Authors:  J Howl; M Wheatley
Journal:  Biochem J       Date:  1996-07-15       Impact factor: 3.857

Review 2.  Isolated hepatocytes: use in experimental and clinical hepatology.

Authors:  A J Strain
Journal:  Gut       Date:  1994-04       Impact factor: 23.059

Review 3.  Liver cell models in in vitro toxicology.

Authors:  A Guillouzo
Journal:  Environ Health Perspect       Date:  1998-04       Impact factor: 9.031

4.  Periportal- and perivenous-enriched hepatocyte couplets: differences in canalicular activity and in response to oxidative stress.

Authors:  J C Wilton; J K Chipman; C J Lawson; A J Strain; R Coleman
Journal:  Biochem J       Date:  1993-06-15       Impact factor: 3.857

5.  Impaired localisation and transport function of canalicular Bsep in taurolithocholate induced cholestasis in the rat.

Authors:  F A Crocenzi; A D Mottino; E J Sánchez Pozzi; J M Pellegrino; E A Rodríguez Garay; P Milkiewicz; M Vore; R Coleman; M G Roma
Journal:  Gut       Date:  2003-08       Impact factor: 23.059

6.  Hepatoprotection with tauroursodeoxycholate and beta muricholate against taurolithocholate induced cholestasis: involvement of signal transduction pathways.

Authors:  P Milkiewicz; M G Roma; E Elias; R Coleman
Journal:  Gut       Date:  2002-07       Impact factor: 23.059

7.  Ca(2+)-dependent protein kinase C isoforms are critical to estradiol 17beta-D-glucuronide-induced cholestasis in the rat.

Authors:  Fernando A Crocenzi; Enrique J Sánchez Pozzi; María Laura Ruiz; Andrés E Zucchetti; Marcelo G Roma; Aldo D Mottino; Mary Vore
Journal:  Hepatology       Date:  2008-12       Impact factor: 17.425

8.  ERK1/2 and p38 MAPKs are complementarily involved in estradiol 17ß-D-glucuronide-induced cholestasis: crosstalk with cPKC and PI3K.

Authors:  Andrea C Boaglio; Andrés E Zucchetti; Flavia D Toledo; Ismael R Barosso; Enrique J Sánchez Pozzi; Fernando A Crocenzi; Marcelo G Roma
Journal:  PLoS One       Date:  2012-11-14       Impact factor: 3.240

9.  Prevention of estradiol 17beta-D-glucuronide-induced canalicular transporter internalization by hormonal modulation of cAMP in rat hepatocytes.

Authors:  Andrés E Zucchetti; Ismael R Barosso; Andrea Boaglio; José M Pellegrino; Elena J Ochoa; Marcelo G Roma; Fernando A Crocenzi; Enrique J Sánchez Pozzi
Journal:  Mol Biol Cell       Date:  2011-08-24       Impact factor: 4.138

10.  Sequential activation of classic PKC and estrogen receptor α is involved in estradiol 17ß-D-glucuronide-induced cholestasis.

Authors:  Ismael R Barosso; Andrés E Zucchetti; Andrea C Boaglio; M Cecilia Larocca; Diego R Taborda; Marcelo G Luquita; Marcelo G Roma; Fernando A Crocenzi; Enrique J Sánchez Pozzi
Journal:  PLoS One       Date:  2012-11-27       Impact factor: 3.240

  10 in total

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