Dokumentenart: | Artikel | ||||||
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Titel eines Journals oder einer Zeitschrift: | Mol Oncol | ||||||
Verlag: | Wiley | ||||||
Ort der Veröffentlichung: | HOBOKEN | ||||||
Datum: | Dezember 2019 | ||||||
Institutionen: | Medizin > Institut für Funktionelle Genomik > Lehrstuhl für Funktionelle Genomik (Prof. Oefner) Medizin > Lehrstuhl für Innere Medizin III (Hämatologie und Internistische Onkologie) Medizin > Institut für Funktionelle Genomik > Lehrstuhl für Statistische Bioinformatik (Prof. Spang) Informatik und Data Science > Fachbereich Bioinformatik > Lehrstuhl für Statistische Bioinformatik (Prof. Spang) | ||||||
Identifikationsnummer: |
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Stichwörter / Keywords: | TUMOR-ASSOCIATED MACROPHAGES; REED-STERNBERG CELLS; MANNOSE RECEPTOR; GENE-EXPRESSION; MICROENVIRONMENT; INTERLEUKIN-13; POLARIZATION; INHIBITOR; CYTOKINE; STRATEGY; CD206; lymphoma; macrophages; tumor microenvironment | ||||||
Dewey-Dezimal-Klassifikation: | 600 Technik, Medizin, angewandte Wissenschaften > 610 Medizin | ||||||
Status: | Veröffentlicht | ||||||
Begutachtet: | Ja, diese Version wurde begutachtet | ||||||
An der Universität Regensburg entstanden: | Zum Teil | ||||||
Dokumenten-ID: | 41288 |
Zusammenfassung
Macrophages (M phi) are abundantly present in the tumor microenvironment and may predict outcome in solid tumors and defined lymphoma subtypes. M phi heterogeneity, the mechanisms of their recruitment, and their differentiation into lymphoma-promoting, alternatively activated M2-like phenotypes are still not fully understood. Therefore, further functional studies are required to understand ...
Zusammenfassung
Macrophages (M phi) are abundantly present in the tumor microenvironment and may predict outcome in solid tumors and defined lymphoma subtypes. M phi heterogeneity, the mechanisms of their recruitment, and their differentiation into lymphoma-promoting, alternatively activated M2-like phenotypes are still not fully understood. Therefore, further functional studies are required to understand biological mechanisms associated with human tumor-associated M phi (TAM). Here, we show that the global mRNA expression and protein abundance of human M phi differentiated in Hodgkin lymphoma (HL)-conditioned medium (CM) differ from those of M phi educated by conditioned media from diffuse large B-cell lymphoma (DLBCL) cells or, classically, by macrophage colony-stimulating factor (M-CSF). Conditioned media from HL cells support TAM differentiation through upregulation of surface antigens such as CD40, CD163, CD206, and PD-L1. In particular, RNA and cell surface protein expression of mannose receptor 1 (MRC1)/CD206 significantly exceed the levels induced by classical M-CSF stimulation in M2-like M phi; this is regulated by interleukin 13 to a large extent. Functionally, high CD206 enhances mannose-dependent endocytosis and uptake of type I collagen. Together with high matrix metalloprotease9 secretion, HL-TAMs appear to be active modulators of the tumor matrix. Preclinical in ovo models show that co-cultures of HL cells with monocytes or M phi support dissemination of lymphoma cells via lymphatic vessels, while tumor size and vessel destruction are decreased in comparison with lymphoma-only tumors. Immunohistology of human HL tissues reveals a fraction of cases feature large numbers of CD206-positive cells, with high MRC1 expression being characteristic of HL-stage IV. In summary, the lymphoma-TAM interaction contributes to matrix-remodeling and lymphoma cell dissemination.
Metadaten zuletzt geändert: 29 Sep 2021 07:41