Sistema FMUSP-HC: Faculdade de Medicina da Universidade de São Paulo (FMUSP) e Hospital das Clínicas da FMUSPARAUJO, Thais L. S.FERNANDES, Carolina G.LAURINDO, Francisco R. M.2017-08-172017-08-172017REDOX BIOLOGY, v.12, p.1004-1010, 20172213-2317https://observatorio.fm.usp.br/handle/OPI/21542Extracellular pools of intracellular molecular chaperones are increasingly evident. The peri/epicellular(pec) pool of the endoplasmic reticulum redox chaperone protein disulfide isomerase-A1(PDI) is involved in thrombosis and vascular remodeling, while PDI externalization routes remain elusive. In endothelial cells, vesicular-type PDI secretion involves classical and unconventional pathways, while in platelets PDI exocytosis involves actin cytoskeleton. However, little is known about pecPDI in vascular smooth muscle cells(VSMC). Here, we showed that VSMC display a robust cell-surface(cs) PDI pool, which binds to cs independently of electrostatic forces. However, contrarily to other cells, soluble secreted PDI pool was undetectable in VSMC. Calcium ionophore A23187 and TNF alpha enhanced VSMC csPDI. Furthermore, VSMC PDI externalization occurred via Golgi-bypass unconventional route, which was independent of cytoskeleton or lysosomes. Secreted PDI was absent in ex vivo wild-type mice aortas but markedly enhanced in PDI-overexpressing mice. Such characterization of VSMC pecPDI reinforces cell-type and context specific routes of PDI externalization.engopenAccessProtein disulfide isomeraseVascular smooth muscle cellUnconventional protein trafficEndoplasmic reticulumCell-surface chaperonesthiol isomerasesactivated plateletsthrombus formationsecretionexpressionmigrationsurfaceendotheliuminhibitorsentryarticleCopyright ELSEVIER SCIENCE BV10.1016/j.redox.2017.04.034Biochemistry & Molecular Biology