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Expression and Localization of TREK-1 K+ Channels in Human Odontoblasts
H. Magloire1,*,
F. Lesage2,
M.L. Couble1,
M. Lazdunski2 and
F. Bleicher1
1 Laboratoire du Développement des Tissus Dentaires, EA 1892, IFR 62, Faculté dOdontologie, Rue G. Paradin, 69372, Lyon cedex 08, France; and
2 Institut de Pharmacologie Moléculaire et Cellulaire, CNRS UPR 441, Sophia Antipolis, 06560 Valbonne, France;

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Figure 1. Analysis of the RT-PCR product of TREK-1 channel mRNAs from cultured odontoblasts (O) and pulp cells (Pc) in vitro. Lane 1 contains the molecular-weight markers (standard VIII, Roche Molecular Biochemicals). The TREK-1 and GAPDH products migrate to a position in good agreement with their respectively predicted sizes of 356 bp and 450 bp.
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Figure 3. In situ hybridization (a,b,c) of a dental pulp section with TREK-1 probe. (a) Note the relative overexpression of transcripts in the coronal odontoblast layer (od) in contrast to pulp cells. (b) In the root region, no significant signal could be identified. (c) TREK-1 mRNA is also detected in the arterioles (ar).
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Journal of Dental Research, Vol. 82, No. 7,
542-545 (2003)
DOI: 10.1177/154405910308200711

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