TSH receptor interaction with the extracellular matrix: role on constitutive activity and sensitivity to hormonal stimulation
N Ghinea, C Baratti-Elbaz… - Molecular …, 2002 - academic.oup.com
N Ghinea, C Baratti-Elbaz, A De Jesus-Lucas, E Milgrom
Molecular Endocrinology, 2002•academic.oup.comUsing immunocytochemistry, we have observed that the TSH receptor (TSHR) is
concentrated at the leading edge of lamellipodia in both cultured human thyroid cells and in
various transfected cells. This segregation of the receptor is due to its interaction with
extracellular matrix (ECM) and specially with fibronectin. The TSHR, which interacts with the
ECM, is known to undergo cleavage by a matrix metalloprotease. The homologous LH
receptor, which does not interact with ECM, is not cleaved. The attachment to the ECM …
concentrated at the leading edge of lamellipodia in both cultured human thyroid cells and in
various transfected cells. This segregation of the receptor is due to its interaction with
extracellular matrix (ECM) and specially with fibronectin. The TSHR, which interacts with the
ECM, is known to undergo cleavage by a matrix metalloprotease. The homologous LH
receptor, which does not interact with ECM, is not cleaved. The attachment to the ECM …
Abstract
Using immunocytochemistry, we have observed that the TSH receptor (TSHR) is concentrated at the leading edge of lamellipodia in both cultured human thyroid cells and in various transfected cells. This segregation of the receptor is due to its interaction with extracellular matrix (ECM) and specially with fibronectin. The TSHR, which interacts with the ECM, is known to undergo cleavage by a matrix metalloprotease. The homologous LH receptor, which does not interact with ECM, is not cleaved.
The attachment to the ECM modifies the functional properties of the receptor: it increases adenylate cyclase stimulation by hormone, whereas PLC stimulation is not modified. Furthermore, the constitutive activity of the TSHR is only observed in attached cells, suggesting that it is dependent on TSHR interaction with the ECM. Thus, aside from its classical properties of hormone binding and signalization through G proteins, the TSHR is also involved in cell-matrix interactions, which modulate its functional properties.
Oxford University Press