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An improved cell culture model based on 2/4/A1 cell monolayers for studies of intestinal drug transport : characterization of transport routes

Tavelin, Staffan (author)
Uppsala universitet,Institutionen för farmaci
Taipalensuu, Jan (author)
Uppsala universitet,Institutionen för farmaci
Hallböök, Finn (author)
Uppsala universitet,Medicinsk utvecklingsbiologi
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Vellonen, Kati-Sisko (author)
Uppsala universitet,Institutionen för farmaci
Moore, Vanessa (author)
Artursson, Per (author)
Uppsala universitet,Institutionen för farmaci
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 (creator_code:org_t)
2003
2003
English.
In: Pharmaceutical research. - 0724-8741 .- 1573-904X. ; 20:3, s. 373-381
  • Journal article (peer-reviewed)
Abstract Subject headings
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  • Purpose. To improve the viability of the 2/4/A1 cell culture model and to investigate different routes of drug transport in this cell line. Methods. Two approaches were taken to decrease apoptosis. First, rat intestinal 2/4/A1 cells were transfected to overexpress the antiapoptotic protein Bcl-2. Second, normal 2/4/A1 cells were cultivated under conditions that stimulate differentiation and limit apoptosis. The monolayer integrity was investigated by transepithelial electrical resistance, permeability, and microscopy. The expression of drug transporters was investigated by RT-PCR, and transport function was assessed using specific markers. Results. Normal 2/4/A1 cells died by apoptosis at 39°C. Bcl-2-expressing 2/4/A1 cells were viable but adopted a morphology of less-differentiated epithelial cells. Optimization of the culture conditions for 2/4/A1 cells inhibited cell death. The integrity was comparable to that of the human jejunum (50 Ω × cm2), making this approach preferable to Bcl-2 overexpression. Transcriptional analysis showed that some (e.g., MDR1), but not all (e.g., PepT1), transporters were found in 2/4/A1 cells. Studies using substrates for PepT1, P-gp, MRP2, and BCRP showed that none of the transporters were functional in 2/4/A1. Conclusions. The improved culture procedure will facilitate the use of 2/4/A1 cells. 2/4/A1 lack several transporters, which makes them a promising alternative to Caco-2 cells and artificial membranes in studies of passive drug transport.

Subject headings

MEDICIN OCH HÄLSOVETENSKAP  -- Medicinska och farmaceutiska grundvetenskaper -- Neurovetenskaper (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Basic Medicine -- Neurosciences (hsv//eng)
MEDICIN OCH HÄLSOVETENSKAP  -- Medicinska och farmaceutiska grundvetenskaper -- Cell- och molekylärbiologi (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Basic Medicine -- Cell and Molecular Biology (hsv//eng)

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Tavelin, Staffan
Taipalensuu, Jan
Hallböök, Finn
Vellonen, Kati-S ...
Moore, Vanessa
Artursson, Per
About the subject
MEDICAL AND HEALTH SCIENCES
MEDICAL AND HEAL ...
and Basic Medicine
and Neurosciences
MEDICAL AND HEALTH SCIENCES
MEDICAL AND HEAL ...
and Basic Medicine
and Cell and Molecul ...
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Pharmaceutical r ...
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Uppsala University

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