Phagocytosis of dying tumor cells by human peritoneal mesothelial cells

Author:

Wagner Britta Janina12,Lindau Dennis1,Ripper Dagmar3,Stierhof York-Dieter3,Glatzle Jörg2,Witte Maria2,Beck Henning45,Keppeler Hildegard6,Lauber Kirsten67,Rammensee Hans-Georg1,Königsrainer Alfred2

Affiliation:

1. Department of Immunology, University of Tübingen, Tübingen 72076, Germany

2. Department of General, Visceral, and Transplantation Surgery, University Hospital Tübingen, Tübingen 72076, Germany

3. Center of Plant Molecular Biology, University of Tübingen, Tübingen 72076, Germany

4. Laboratory for NeuroRegeneration and Repair, Center for Neurology, Hertie Institute for Clinical Brain Research, University of Tübingen, Tübingen 72076, Germany

5. Graduate School for Cellular and Molecular Neurosciences, University of Tübingen, Tübingen 72076, Germany

6. Department of Internal Medicine I, University of Tübingen, Tübingen 72076, Germany

7. Department of Radiation Oncology, LMU Munich, Munich 81377, Germany

Abstract

Peritoneal carcinomatosis is an advanced form of metastatic disease characterized by cancer cell dissemination onto the peritoneum. It is commonly observed in ovarian and colorectal cancers and is associated with poor patient survival. Novel therapies consist of cytoreductive surgery in combination with intraperitoneal chemotherapy, aiming at tumor cell death induction. The resulting dying tumor cells are considered to be eliminated by professional as well as semi-professional phagocytes. In the present study, we have identified a hitherto unknown type of ‘amateur’ phagocyte in this environment: human peritoneal mesothelial cells (HMCs). We demonstrate that HMCs engulf corpses of dying ovarian and colorectal cancer cells, as well as other types of apoptotic cells. Flow cytometric, confocal and electron microscopical analyses revealed that HMCs ingest dying cell fragments in a dose- and time-dependent manner and the internalized material subsequently traffics into late phagolysosomes. Regarding the mechanisms of prey cell recognition, our results show that HMCs engulf apoptotic corpses in a serum-dependent and -independent fashion and quantitative real-time PCR (qRT-PCR) analyses revealed that diverse opsonin receptor systems orchestrating dying cell clearance are expressed in HMCs at high levels. Our data strongly suggest that HMCs contribute to dying cell removal in the peritoneum, and future studies will elucidate in what manner this influences tumor cell dissemination and the antitumor immune response.

Publisher

The Company of Biologists

Subject

Cell Biology

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