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Blatner, N.R.* ; Bonertz, A.* ; Beckhove, P.* ; Cheon, E.C.* ; Krantz, S.B.* ; Strouch, M.* ; Weitz, J.* ; Koch, M.* ; Halverson, A.L.* ; Bentrem, D.J.* ; Khazaie, K.*

In colorectal cancer mast cells contribute to systemic regulatory T-cell dysfunction.

Proc. Natl. Acad. Sci. U.S.A. 107, 6430-6435 (2010)
DOI Verlagsversion bestellen
T-regulatory cells (Treg) and mast cells (MC) are abundant in colorectal cancer (CRC) tumors. Interaction between the two is known to promote immune suppression or loss of Treg functions and autoimmunity. Here, we demonstrate that in both human CRC and murine polyposis the outcome of this interaction is the generation of potently immune suppressive but proinflammatory Treg (DeltaTreg). These Treg shut down IL10, gain potential to express IL17, and switch from suppressing to promoting MC expansion and degranulation. This change is also brought about by direct coculture of MC and Treg, or culture of Treg in medium containing IL6 and IL2. IL6 deficiency in the bone marrow of mice susceptible to polyposis eliminated IL17 production by the polyp infiltrating Treg, but did not significantly affect the growth of polyps or the generation of proinflammatory Treg. IL6-deficient MC could generate proinflammatory Treg. Thus, MC induce Treg to switch function and escalate inflammation in CRC without losing T-cell-suppressive properties. IL6 and IL17 are not needed in this process.
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Publikationstyp Artikel: Journalartikel
Dokumenttyp Wissenschaftlicher Artikel
ISSN (print) / ISBN 0027-8424
e-ISSN 1091-6490
Quellenangaben Band: 107, Heft: 14, Seiten: 6430-6435 Artikelnummer: , Supplement: ,
Verlag National Academy of Sciences
Begutachtungsstatus
Institut(e) Institute for Pancreatic Beta Cell Research (IPI)