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2017 ; 8
(49
): 84928-84944
Nephropedia Template TP
gab.com Text
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PDAC-derived exosomes enrich the microenvironment in MDSCs in a SMAD4-dependent
manner through a new calcium related axis
#MMPMID29156694
Basso D
; Gnatta E
; Padoan A
; Fogar P
; Furlanello S
; Aita A
; Bozzato D
; Zambon CF
; Arrigoni G
; Frasson C
; Franchin C
; Moz S
; Brefort T
; Laufer T
; Navaglia F
; Pedrazzoli S
; Basso G
; Plebani M
Oncotarget
2017[Oct]; 8
(49
): 84928-84944
PMID29156694
show ga
Tumor genetics and escape from immune surveillance concur in the poor prognosis
of PDAC. In this study an experimental model was set up to verify whether SMAD4,
deleted in about 55% PDAC and associated with poor prognosis, is involved in
determining immunosuppression through Exosomes (Exo). Potential mechanisms and
mediators underlying SMAD4-dependent immunosuppression were evaluated by studying
intracellular calcium (Fluo-4), Exo-miRNAs (microarray) and Exo-proteins (SILAC).
Two PDAC cell lines expressing (BxPC3-SMAD4+) or not-expressing (BxPC3) SMAD4
were used to prepare Exo-enriched conditioned media, employed in experiments with
blood donors PBMCs. Exo expanded myeloid derived suppressor cells (gMDSC and
mMDSC, flow cytometry) and altered intracellular calcium fluxes in an SMAD4
dependent manner. BxPC3-SMAD4+, but mainly BxPC3 Exo, increased calcium fluxes of
PBMCs (p = 0.007) and this increased intracellular calcium trafficking
characterized mMDSCs. The analysis of de-regulated Exo-miRNAs and transfection
experiments revealed hsa-miR-494-3p and has-miR-1260a as potential mediators of
SMAD4-associated de-regulated calcium fluxes. Eleven main biological processes
were identified by the analysis of SMAD4-associated de-regulated Exo-proteins,
including translation, cell adhesion, cell signaling and glycolysis. A reverse
Warburg effect was observed by treating PBMCs with PDAC-derived Exo: BxPC3 Exo
induced a higher glucose consumption and lactate production than BxPC3-SMAD4+
Exo. CONCLUSION: PDAC-derived Exo from cells with, but mainly from those without
SMAD4 expression, create an immunosuppressive myeloid cell background by
increasing calcium fluxes and glycolysis through the transfer of SMAD4-related
differentially expressed miRNAs and proteins.