Limits...
Expression pattern of thyroid hormone transporters in the postnatal mouse brain.

Müller J, Heuer H - Front Endocrinol (Lausanne) (2014)

Bottom Line: Whereas Mct8 and Lat2 showed an overlapping neuronal mRNA expression pattern in the cerebral cortex, hippocampus, and in the hypothalamus, Oatp1c1 and Lat1 specific signals were most prominent in capillary endothelial cells throughout the CNS.In the choroid plexus, expression of three transporters (Mct8, Lat2, and Oatp1c1) could be detected, whereas in other brain areas (e.g., striatum, thalamus, and brain stem nuclei) only one of the transporter candidates appeared to be present.Overall, our study revealed a distinct mRNA distribution pattern for each of the TH transporter candidates.

View Article: PubMed Central - PubMed

Affiliation: Leibniz Institute for Age Research - Fritz Lipmann Institute , Jena , Germany.

ABSTRACT
For a comprehensive description of the tissue-specific thyroidal state under normal as well as under pathophysiological conditions it is of utmost importance to include thyroid hormone (TH) transporters in the analysis as well. The current knowledge of the cell-specific repertoire of TH transporters, however, is still rather limited, although several TH transporting proteins have been identified. Here, we describe the temporal and spatial distribution pattern of the most prominent TH transporters in the postnatal mouse brain. For that purpose, we performed radioactive in situ hybridization studies in order to analyze the cellular mRNA expression pattern of the monocarboxylate transporters Mct8 and Mct10, the L-type amino acid transporters Lat1 and Lat2 as well as the organic anion transporting peptide Oatp1c1 at different postnatal time points. Highest TH transporter expression levels in the CNS were observed at postnatal day 6 and 12, while hybridization signal intensities visibly declined after the second postnatal week. The only exception was Mct10 for which the strongest signals could be observed in white matter regions at postnatal day 21 indicating that this transporter is preferentially expressed in mature oligodendrocytes. Whereas Mct8 and Lat2 showed an overlapping neuronal mRNA expression pattern in the cerebral cortex, hippocampus, and in the hypothalamus, Oatp1c1 and Lat1 specific signals were most prominent in capillary endothelial cells throughout the CNS. In the choroid plexus, expression of three transporters (Mct8, Lat2, and Oatp1c1) could be detected, whereas in other brain areas (e.g., striatum, thalamus, and brain stem nuclei) only one of the transporter candidates appeared to be present. Overall, our study revealed a distinct mRNA distribution pattern for each of the TH transporter candidates. Further studies will reveal to which extent these transporters contribute to the cell-specific TH uptake and efflux in the mouse CNS.

No MeSH data available.


Illustration of TH transporter mRNA expression in the murine forebrain. Coronal cryosections of mouse brains collected at different postnatal days were hybridized with radioactively labeled riboprobes specific for Mct8 (A1–A4), Lat2 (B1–B4), Oatp1c1 (C1–C4), Lat1 (D1–D4), and Mct10 (E1–E4). Dark-field autoradiograms illustrate the mRNA expression patterns at the level of the striatum (CPu, caudate–putamen) around Bregma 0.5 mm. VI, layer 6 of the cerebral cortex; cc, corpus callosum; Cg, cingulate cortex, LV, lateral ventricle; Pir, piriform cortex; SP, subplate neurons (cerebral cortex).
© Copyright Policy - open-access
Related In: Results  -  Collection

License
getmorefigures.php?uid=PMC4061481&req=5

Figure 1: Illustration of TH transporter mRNA expression in the murine forebrain. Coronal cryosections of mouse brains collected at different postnatal days were hybridized with radioactively labeled riboprobes specific for Mct8 (A1–A4), Lat2 (B1–B4), Oatp1c1 (C1–C4), Lat1 (D1–D4), and Mct10 (E1–E4). Dark-field autoradiograms illustrate the mRNA expression patterns at the level of the striatum (CPu, caudate–putamen) around Bregma 0.5 mm. VI, layer 6 of the cerebral cortex; cc, corpus callosum; Cg, cingulate cortex, LV, lateral ventricle; Pir, piriform cortex; SP, subplate neurons (cerebral cortex).

Mentions: The aim of the current study was to perform a comparative analysis of TH transporter expression patterns in the murine CNS at different postnatal time point. In particular, we aimed to determine the cellular distribution pattern of the transporters Mct8 (Slc16a2), Mct10 (Slc16a10), Lat1 (Slc7a5), Lat2 (Slc7a8), and Oatp1c1 (Slco1c1) that have all been described to facilitate the cellular transport of TH (25). Since only for a subset of these proteins specific antibodies are available, we employed a highly sensitive ISH technique using 35S-labeled RNA probes. Brains were collected from C57/Bl6 male mice at postnatal day 6 (P6), P12, P21, and P84 and consecutive frozen brain sections were subjected to the ISH procedure as described previously (24). For the description of the mRNA distribution at a cellular resolution, nuclear emulsion coated slides were examined under dark-field illumination using a light-microscope. Each antisense probe indeed produced a positive hybridization signal with a highly distinct cellular distribution pattern as visualized exemplarily in Figures 1–4 for four different anatomical regions. In particular, Figure 1 illustrates cortical and striatal expression at around Bregma 0.50 mm; Figure 2 (between Bregma −1.8 and −2.2 mm) shows mRNA expression patterns in the cortex, hippocampus, thalamus, and hypothalamus; Figure 3 depicts TH transporter expression between Bregma −3.4 and −4.4 including mesencephalic areas; Figure 4 shows cerebellar and brainstem expression pattern around Bregma −6.2 [according to Franklin and Paxinos (26)].


Expression pattern of thyroid hormone transporters in the postnatal mouse brain.

Müller J, Heuer H - Front Endocrinol (Lausanne) (2014)

Illustration of TH transporter mRNA expression in the murine forebrain. Coronal cryosections of mouse brains collected at different postnatal days were hybridized with radioactively labeled riboprobes specific for Mct8 (A1–A4), Lat2 (B1–B4), Oatp1c1 (C1–C4), Lat1 (D1–D4), and Mct10 (E1–E4). Dark-field autoradiograms illustrate the mRNA expression patterns at the level of the striatum (CPu, caudate–putamen) around Bregma 0.5 mm. VI, layer 6 of the cerebral cortex; cc, corpus callosum; Cg, cingulate cortex, LV, lateral ventricle; Pir, piriform cortex; SP, subplate neurons (cerebral cortex).
© Copyright Policy - open-access
Related In: Results  -  Collection

License
Show All Figures
getmorefigures.php?uid=PMC4061481&req=5

Figure 1: Illustration of TH transporter mRNA expression in the murine forebrain. Coronal cryosections of mouse brains collected at different postnatal days were hybridized with radioactively labeled riboprobes specific for Mct8 (A1–A4), Lat2 (B1–B4), Oatp1c1 (C1–C4), Lat1 (D1–D4), and Mct10 (E1–E4). Dark-field autoradiograms illustrate the mRNA expression patterns at the level of the striatum (CPu, caudate–putamen) around Bregma 0.5 mm. VI, layer 6 of the cerebral cortex; cc, corpus callosum; Cg, cingulate cortex, LV, lateral ventricle; Pir, piriform cortex; SP, subplate neurons (cerebral cortex).
Mentions: The aim of the current study was to perform a comparative analysis of TH transporter expression patterns in the murine CNS at different postnatal time point. In particular, we aimed to determine the cellular distribution pattern of the transporters Mct8 (Slc16a2), Mct10 (Slc16a10), Lat1 (Slc7a5), Lat2 (Slc7a8), and Oatp1c1 (Slco1c1) that have all been described to facilitate the cellular transport of TH (25). Since only for a subset of these proteins specific antibodies are available, we employed a highly sensitive ISH technique using 35S-labeled RNA probes. Brains were collected from C57/Bl6 male mice at postnatal day 6 (P6), P12, P21, and P84 and consecutive frozen brain sections were subjected to the ISH procedure as described previously (24). For the description of the mRNA distribution at a cellular resolution, nuclear emulsion coated slides were examined under dark-field illumination using a light-microscope. Each antisense probe indeed produced a positive hybridization signal with a highly distinct cellular distribution pattern as visualized exemplarily in Figures 1–4 for four different anatomical regions. In particular, Figure 1 illustrates cortical and striatal expression at around Bregma 0.50 mm; Figure 2 (between Bregma −1.8 and −2.2 mm) shows mRNA expression patterns in the cortex, hippocampus, thalamus, and hypothalamus; Figure 3 depicts TH transporter expression between Bregma −3.4 and −4.4 including mesencephalic areas; Figure 4 shows cerebellar and brainstem expression pattern around Bregma −6.2 [according to Franklin and Paxinos (26)].

Bottom Line: Whereas Mct8 and Lat2 showed an overlapping neuronal mRNA expression pattern in the cerebral cortex, hippocampus, and in the hypothalamus, Oatp1c1 and Lat1 specific signals were most prominent in capillary endothelial cells throughout the CNS.In the choroid plexus, expression of three transporters (Mct8, Lat2, and Oatp1c1) could be detected, whereas in other brain areas (e.g., striatum, thalamus, and brain stem nuclei) only one of the transporter candidates appeared to be present.Overall, our study revealed a distinct mRNA distribution pattern for each of the TH transporter candidates.

View Article: PubMed Central - PubMed

Affiliation: Leibniz Institute for Age Research - Fritz Lipmann Institute , Jena , Germany.

ABSTRACT
For a comprehensive description of the tissue-specific thyroidal state under normal as well as under pathophysiological conditions it is of utmost importance to include thyroid hormone (TH) transporters in the analysis as well. The current knowledge of the cell-specific repertoire of TH transporters, however, is still rather limited, although several TH transporting proteins have been identified. Here, we describe the temporal and spatial distribution pattern of the most prominent TH transporters in the postnatal mouse brain. For that purpose, we performed radioactive in situ hybridization studies in order to analyze the cellular mRNA expression pattern of the monocarboxylate transporters Mct8 and Mct10, the L-type amino acid transporters Lat1 and Lat2 as well as the organic anion transporting peptide Oatp1c1 at different postnatal time points. Highest TH transporter expression levels in the CNS were observed at postnatal day 6 and 12, while hybridization signal intensities visibly declined after the second postnatal week. The only exception was Mct10 for which the strongest signals could be observed in white matter regions at postnatal day 21 indicating that this transporter is preferentially expressed in mature oligodendrocytes. Whereas Mct8 and Lat2 showed an overlapping neuronal mRNA expression pattern in the cerebral cortex, hippocampus, and in the hypothalamus, Oatp1c1 and Lat1 specific signals were most prominent in capillary endothelial cells throughout the CNS. In the choroid plexus, expression of three transporters (Mct8, Lat2, and Oatp1c1) could be detected, whereas in other brain areas (e.g., striatum, thalamus, and brain stem nuclei) only one of the transporter candidates appeared to be present. Overall, our study revealed a distinct mRNA distribution pattern for each of the TH transporter candidates. Further studies will reveal to which extent these transporters contribute to the cell-specific TH uptake and efflux in the mouse CNS.

No MeSH data available.