RESUMO
Previously, by employing 3D organotypic tissue culture and patient-derived xenograft (PDX) model, oral myxoma response to a MAPK/MEK inhibitor was observed. Gross examination of the tumour fragments obtained after 55 days of PDX grafting revealed increased capsule vascularization. Microscopic analyses showed blood capillaries intermixed with myxoma cells, but the origin of these capillaries, from mice or humans, was not established. This study aimed to investigate whether the endothelial cells observed in the myxoma PDX model are derived from the mouse or from the primary human tumour. Immunohistochemistry was performed on five tumour fragments from the PDX of myxoma after 55 days of implantation in mice. Immunopositivity for antibodies against human (HLA-ABC) and mouse (H2 Db/H2-D1) major histocompatibility complex class I (MHCI) was assessed in the endothelial cells. The endothelial cells in the PDX fragments revealed a membrane staining for the human MHCI protein in the PDX tumour and adjacent connective tissue capsule, indicating that capillaries were derived from the human tumour fragment. Considering the probable human origin of the endothelial cells from capillary blood vessels in the myxoma PDX, we conclude that this PDX model is an interesting model to study myxoma angiogenesis.
Assuntos
Células Endoteliais , Mixoma , Animais , Modelos Animais de Doenças , Xenoenxertos , Humanos , Camundongos , Neovascularização Patológica , Ensaios Antitumorais Modelo de XenoenxertoRESUMO
The sexual segment of the kidney (SSK) is a hypertrophied region of the nephron, which occurs in males of most squamate species that have been investigated, at least, during the active season. Many studies have shown that the SSK has a seasonal secretory cycle that could be correlated to the mating season, testicular activity, and androgen synthesis. However, to date, no study has investigated the presence of androgen receptors (AR) in cells of the SSK, nor the relation between the expression of AR, testosterone levels, and testicular condition. The SSK in Crotalus durissus corresponds to the distal segment of the nephron and presents a peak of hypertrophy during the period of testicular activity (spermatogenesis) and high testosterone levels, suggesting that seasonal variation of the SSK might be under the control of androgens. Testosterone concentrations and expression of AR varied seasonally with increased values for both parameters directly correlated to hypertrophy of the SSK. This study is, therefore, the first to target the SSK of a tropical snake and to establish a relationship between the secretory cycle of the SSK, testicular cycle, and levels of androgens. Furthermore, this study is the first to identify the presence of AR in the nucleus of the SSK cells.