“…Recent studies have shown that extracellular N-terminus within adhesive GPCRs can act as an anchor mechanism to the extracellular matrix (ECM), playing key roles in response to mechanical tension and in the control of their activity [ 37 , 38 ]. A recent revision approaches the different GPCRs which can be directly modulated by mechanical forces, highlighting the critical role of specific GPCRs in mechanotransduction such as adhesion GPCRs, APJ/apelin, AT 1 R, B 2 AR, B 2 R, ET 1 AR, GPR68, H 1 R, M 5 R PTH 1 R, all of them very relevant at vascular level [ 35 , 36 , 39 , 40 , 41 ]. Since most GPCRs contain at least one N-glycan chain in their extracellular domain, further investigation will be required to address their patho-physiological functions.…”