Abstract

There is growing evidence that equine papillomavirus type 2 (EcPV2) infection is etiologically associated with the development of genital squamous cell carcinoma (SCC) and precursor lesions in equids. However, the precise mechanisms underlying neoplastic progression remain unknown. To allow the study of EcPV2-induced carcinogenesis, we aimed to establish a primary equine cell culture model of EcPV2 infection. Three-dimensional (3D) raft cultures were generated from equine penile perilesional skin, plaques and SCCs. Using histological, molecular biological and immunohistochemical methods, rafts versus corresponding natural tissue sections were compared with regard to morphology, presence of EcPV2 DNA, presence and location of EcPV2 gene transcripts and expression of epithelial, mesenchymal and tumor/proliferation markers. Raft cultures from perilesional skin harboring only a few EcPV2-positive (EcPV2+) cells accurately recapitulated the differentiation process of normal skin, whilst rafts from EcPV2+ penile plaques were structurally organized but showed early hyperplasia. Rafts from EcPV2+ SCCs exhibited pronounced hyperplasia and marked dysplasia. Raft levels of EcPV2 oncogene transcription (E6/E7) and expression of tumor/proliferation markers p53, Ki67 and MCM7 expression positively correlated with neoplastic progression, again reflecting the natural situation. Three-dimensional raft cultures accurately reflected major features of corresponding ex vivo material, thus constituting a valuable new research model to study EcPV2-induced carcinogenesis.

Highlights

  • Primary equine keratinocytes from penile squamous cell carcinoma (SCC), penile plaques and/or perilesional skin from penile tumor margins of three horses were isolated and expanded in cell culture

  • DNA isolated from original tissue and derived cell culture aliquots tested positive by equine GAPDH PCR, confirming the PCR suitability and equine origin of the cultured cells

  • Raft cultures established from perilesional penile skin were clearly organized into a basal, a spinous and a cornified cell layer

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Summary

Introduction

Papillomaviruses (PVs) belong to a family of small mucocutaneous viruses that can induce benign disease or cancer in humans and a wide range of animals [1]. PVs consist of a non-enveloped capsid enclosing a relatively short (~8 kbp), circular dsDNA genome consisting of an early region (E), a late region (L) and a non-coding long control region (LCR). The E region comprises open reading frames (ORFs) encoding for regulatory proteins such as E1, E2 and E4, and transforming proteins such as E6, E7 and frequently E5. The late (L) region encodes the viral capsid proteins L1 and L2. The LCR that is located between the

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