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Forschungsdatenbank PMU-SQQUID

Circulating B-cell chronic lymphocytic leukemia cells display impaired migration to lymph nodes and bone marrow.
Hartmann, TN; Grabovsky, V; Wang, W; Desch, P; Rubenzer, G; Wollner, S; Binsky, I; Vallon-Eberhard, A; Sapoznikov, A; Burger, M; Shachar, I; Haran, M; Honczarenko, M; Greil, R; Alon, R;
Cancer Res. 2009; 69(7):3121-3130
Originalarbeiten (Zeitschrift)

PMU-Autor/inn/en

Brachtl Gabriele
Greil Richard
Hartmann Tanja

Abstract

Homing to secondary lymphoid organs and bone marrow (BM) is a central aspect of leukemic pathophysiology. We investigated the roles of the two major lymphocyte integrins LFA-1 and VLA-4 on B-cell chronic lymphocytic leukemia (CLL) cells in these processes. We found that the majority of CLL cells expressed significantly reduced LFA-1 due to low beta2 integrin transcripts. VLA-4 expression was heterogeneous but underwent rapid activation by the BM chemokine CXCL12. CLL cells failed to transmigrate across VCAM-1-expressing, ICAM-1-expressing, and CXCL12-expressing endothelium, whereas when LFA-1 expression was regained in subsets of CLL cells, these lymphocytes rapidly transmigrated the endothelium. Furthermore, when injected into tail veins of immunodeficient mice, normal B cells rapidly homed to lymph nodes (LN) in a LFA-1-dependent manner, whereas CLL cells did not. Nevertheless, only residual CLL subsets could reenter BM, whereas both normal and CLL cells homed to the mice spleen in an LFA-1-independent and VLA-4-independent manner. Our results suggest that CLL cells have a reduced capacity to adhere and transmigrate through multiple vascular endothelial beds and poorly home to lymphoid organs other than spleen. Integrin blocking could thus be an efficient strategy to prevent circulating CLL cells from reaching prosurvival niches in LNs and BM but not in spleen.


Useful keywords (using NLM MeSH Indexing)

Animals

Bone Marrow/immunology*

Bone Marrow/pathology

Cell Movement/immunology*

Chemokines/immunology

Endothelial Cells/immunology

Endothelial Cells/pathology

Humans

Integrin alpha4beta1/immunology

Leukemia, Lymphocytic, Chronic, B-Cell/blood

Leukemia, Lymphocytic, Chronic, B-Cell/immunology*

Leukemia, Lymphocytic, Chronic, B-Cell/pathology

Lymph Nodes/immunology*

Lymph Nodes/pathology

Lymphocyte Function-Associated Antigen-1/biosynthesis

Lymphocyte Function-Associated Antigen-1/immunology

Mice

Mice, Inbred NOD

Mice, SCID

Neoplastic Cells, Circulating/immunology*

Neoplastic Cells, Circulating/pathology

Spleen/immunology