TY - JOUR
AU - O'Connor, Tracy
AU - Zhou, Xiaolan
AU - Kosla, Jan
AU - Adili, Arlind
AU - Garcia Beccaria, Maria
AU - Kotsiliti, Elena
AU - Pfister, Dominik
AU - Johlke, Anna-Lena
AU - Sinha, Ankit
AU - Sankowski, Roman
AU - Schick, Markus
AU - Lewis, Richard
AU - Dokalis, Nikolaos
AU - Seubert, Bastian
AU - Höchst, Bastian
AU - Inverso, Donato
AU - Heide, Danijela
AU - Zhang, Wenlong
AU - Weihrich, Petra
AU - Manske, Katrin
AU - Wohlleber, Dirk
AU - Anton, Martina
AU - Hoellein, Alexander
AU - Seleznik, Gitta
AU - Bremer, Juliane
AU - Bleul, Sabine
AU - Augustin, Hellmut G
AU - Scherer, Florian
AU - Koedel, Uwe
AU - Weber, Achim
AU - Protzer, Ulrike
AU - Förster, Reinhold
AU - Wirth, Thomas
AU - Aguzzi, Adriano
AU - Meissner, Felix
AU - Prinz, Marco
AU - Baumann, Bernd
AU - Höpken, Uta E
AU - Knolle, Percy A
AU - von Baumgarten, Louisa
AU - Keller, Ulrich
AU - Heikenwälder, Mathias
TI - Age-Related Gliosis Promotes Central Nervous System Lymphoma through CCL19-Mediated Tumor Cell Retention.
JO - Cancer cell
VL - 36
IS - 3
SN - 1535-6108
CY - New York, NY
PB - Elsevier
M1 - DKFZ-2019-02268
SP - 250 - 267.e9
PY - 2019
N1 - DKFZ-ZMBH Alliance
AB - How lymphoma cells (LCs) invade the brain during the development of central nervous system lymphoma (CNSL) is unclear. We found that NF-κB-induced gliosis promotes CNSL in immunocompetent mice. Gliosis elevated cell-adhesion molecules, which increased LCs in the brain but was insufficient to induce CNSL. Astrocyte-derived CCL19 was required for gliosis-induced CNSL. Deleting CCL19 in mice or CCR7 from LCs abrogated CNSL development. Two-photon microscopy revealed LCs transiently entering normal brain parenchyma. Astrocytic CCL19 enhanced parenchymal CNS retention of LCs, thereby promoting CNSL formation. Aged, gliotic wild-type mice were more susceptible to forming CNSL than young wild-type mice, and astrocytic CCL19 was observed in both human gliosis and CNSL. Therefore, CCL19-CCR7 interactions may underlie an increased age-related risk for CNSL.
LB - PUB:(DE-HGF)16
C6 - pmid:31526758
DO - DOI:10.1016/j.ccell.2019.08.001
UR - https://inrepo02.dkfz.de/record/144843
ER -