Abstract

Merkel cell polyomavirus (MCPyV) is a human polyomavirus causally linked to the development of Merkel cell carcinoma (MCC), an aggressive malignancy that largely arises within the dermis of the skin. In this study, we recapitulate the histopathology of human MCC tumors in vitro using an organotypic (raft) culture system that is traditionally used to recapitulate the dermal and epidermal equivalents of skin in three dimensions (3D). In the optimal culture condition, MCPyV+ MCC cells were embedded in collagen between the epidermal equivalent comprising human keratinocytes and a dermal equivalent containing fibroblasts, resulting in MCC-like lesions arising within the dermal equivalent. The presence and organization of MCC cells within these dermal lesions were characterized through biomarker analyses. Interestingly, co-culture of MCPyV+ MCC together with keratinocytes specifically within the epidermal equivalent of the raft did not reproduce human MCC morphology, nor were any keratinocytes necessary for MCC-like lesions to develop in the dermal equivalent. This 3D tissue culture system provides a novel in vitro platform for studying the role of MCPyV T antigens in MCC oncogenesis, identifying additional factors involved in this process, and for screening potential MCPyV+ MCC therapeutic strategies.

Highlights

  • Merkel cell polyomavirus (MCPyV) was discovered in 2008 in the context of a rare but highly lethal form of skin cancer, Merkel cell carcinoma (MCC) [1]

  • The MCPyV+ MCC cell line included in rafts was MKL-1, a classical MCC cell line derived from a metastatic MCC tumor isolated from a 26-year-old male [31]

  • We describe the establishment of a three-dimensional in vitro model system that recapitulates the histopathology of MCPyV+ MCC in human skin

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Summary

Introduction

Merkel cell polyomavirus (MCPyV) was discovered in 2008 in the context of a rare but highly lethal form of skin cancer, Merkel cell carcinoma (MCC) [1]. MCPyV is one of multiple recently identified human polyomaviruses (reviewed in [4,5]). MCPyV has a double-stranded, circular DNA genome encoding “early” and “late” genes [1]. Studies suggest that the most likely tropism of MCPyV is either epithelial cells and/or dermal fibroblasts [6,11,12]. Only dermal fibroblasts [8] and HEK293 cells [13] have been reported to support the viral life cycle of MCPyV in vitro and result in the production of infectious progeny virions capable of serial transmission. The development of in vitro tissue culture conditions that recapitulate the histopathology of MCC could help scientists study the role of MCPyV in the genesis of this deadly disease

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