TY - JOUR
T1 - Human female hair follicles are a direct, nonclassical target for thyroid-stimulating hormone
AU - Bodó, Enikö
AU - Kromminga, Arno
AU - Bíró, Tamás
AU - Borbíró, István
AU - Gáspár, Erzsébet
AU - Zmijewski, Michal A.
AU - Van Beek, Nina
AU - Langbein, Lutz
AU - Slominski, Andrzej T.
AU - Paus, Ralf
N1 - Funding Information:
We thank U. Duske and A. Becker for excellent technical assistance. This study was supported in part by a grant from Deutsche Forschungsgemeinschaft to RP. The support of Dr W. Funk (Klinik Dr Kozlowski, Munich, Germany), Dr W. Moser (Moser-Klinik, Augsburg, Germany), and Dr Bräutigam (Holstentor Klinik, Lübeck, Germany) for supplying us with facelift skin samples is most gratefully acknowledged. We are grateful to Dr J. Klöpper and N. Dörwald (Department of Dermatology, University Hospital Schleswig-Holstein, University of Lübeck, Lübeck, Germany) for supplying telogen skin and to Dr B. Czarnocka (Department of Biochemistry, Medical Centre of postgraduate Education, Warsaw, Poland) for supplying TPO antibody. Finally, we thank Dr Björn E. Wenzel for most helpful expert advice throughout this study and for valuable suggestions for improving the paper.
PY - 2009/5
Y1 - 2009/5
N2 - Pituitary thyroid-stimulating hormone (TSH) regulates thyroid hormone synthesis via receptors (TSH-R) expressed on thyroid epithelial cells. As the hair follicle (HF) is uniquely hormone-sensitive and, hypothyroidism with its associated, increased TSH serum levels clinically can lead to hair loss, we asked whether human HFs are a direct target for TSH. Here, we report that normal human scalp skin and microdissected human HFs express TSH-R mRNA. TSH-R-like immunoreactivity is limited to the mesenchymal skin compartments in situ. TSH may alter HF mesenchymal functions, as it upregulates α-smooth muscle actin expression in HF fibroblasts. TSH-R stimulation by its natural ligand in organ culture changes the expression of several genes of human scalp HFs (for example keratin K5), upregulates the transcription of classical TSH target genes and enhances cAMP production. Although the functional role of TSH in human HF biology awaits further dissection, these findings document that intracutaneous TSH-Rs are fully functional in situ and that HFs of female individuals are direct targets for nonclassical, extrathyroidal TSH bioregulation. This suggests that organ-cultured scalp HFs provide an instructive and physiologically relevant human model for exploring nonclassical functions of TSH, in and beyond the skin.
AB - Pituitary thyroid-stimulating hormone (TSH) regulates thyroid hormone synthesis via receptors (TSH-R) expressed on thyroid epithelial cells. As the hair follicle (HF) is uniquely hormone-sensitive and, hypothyroidism with its associated, increased TSH serum levels clinically can lead to hair loss, we asked whether human HFs are a direct target for TSH. Here, we report that normal human scalp skin and microdissected human HFs express TSH-R mRNA. TSH-R-like immunoreactivity is limited to the mesenchymal skin compartments in situ. TSH may alter HF mesenchymal functions, as it upregulates α-smooth muscle actin expression in HF fibroblasts. TSH-R stimulation by its natural ligand in organ culture changes the expression of several genes of human scalp HFs (for example keratin K5), upregulates the transcription of classical TSH target genes and enhances cAMP production. Although the functional role of TSH in human HF biology awaits further dissection, these findings document that intracutaneous TSH-Rs are fully functional in situ and that HFs of female individuals are direct targets for nonclassical, extrathyroidal TSH bioregulation. This suggests that organ-cultured scalp HFs provide an instructive and physiologically relevant human model for exploring nonclassical functions of TSH, in and beyond the skin.
UR - http://www.scopus.com/inward/record.url?scp=65049087930&partnerID=8YFLogxK
U2 - 10.1038/jid.2008.361
DO - 10.1038/jid.2008.361
M3 - Journal articles
C2 - 19052559
AN - SCOPUS:65049087930
SN - 0022-202X
VL - 129
SP - 1126
EP - 1139
JO - Journal of Investigative Dermatology
JF - Journal of Investigative Dermatology
IS - 5
ER -