Immunohistochemical assessment of Pax8 expression during pancreatic islet development and in human neuroendocrine tumors

被引:0
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作者
Petra I. Lorenzo
Carmen M. Jimenez Moreno
Irene Delgado
Nadia Cobo-Vuilleumier
Raphael Meier
Lourdes Gomez-Izquierdo
Thierry Berney
Rocio Garcia-Carbonero
Anabel Rojas
Benoit R. Gauthier
机构
[1] Department of Stem Cells,Pancreatic Islet Development and Regeneration Unit
[2] CABIMER-Andalusian Center for Molecular Biology and Regenerative Medicine,Pancreatic Islets and Stem Cells Unit
[3] Department of Stem Cells,Cell Isolation and Transplantation Center
[4] CABIMER-Andalusian Center for Molecular Biology and Regenerative Medicine,Servicio de Oncologia, Hospital Universitario Virgen del Rocio
[5] Department of Surgery,undefined
[6] Geneva University Hospitals,undefined
[7] Servicio de Anatomia Patologica,undefined
[8] Hospital Universitario Virgen del Rocio,undefined
[9] Instituto de Biomedicina de Sevilla (IBIS),undefined
来源
关键词
Pancreatic islet; Transcription factor; Pax genes; Neuroendocrine tumors; Antibody cross-reactivity;
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摘要
The paired box transcription factor Pax8 is critical for development of the eye, thyroid gland as well as the urinary and reproductive organs. In adult, Pax8 overexpression is associated with kidney, ovarian and thyroid tumors and has emerged as a specific marker for these cancers. Recently, Pax8 expression was also reported in human pancreatic islets and in neuroendocrine tumors, identifying Pax8 as a novel member of the Pax family expressed in the pancreas. Herein, we sought to provide a comprehensive analysis of Pax8 expression during pancreogenesis and in adult islets. Immunohistochemical analysis using the most employed Pax8 polyclonal antibody revealed strong nuclear staining in the developing mouse pancreas and in mature human and mouse islets. Astonishingly, Pax8 mRNA in mouse islets was undetectable while human islets exhibited low levels. These discrepancies raised the possibility of antibody cross-reactivity. This premise was confirmed by demonstrating that the polyclonal Pax8 antibody also recognized the islet-enriched Pax6 protein both by Western blotting and immunohistochemistry. Thus, in islets polyclonal Pax8 staining corresponds mainly to Pax6. In order to circumvent this caveat, a novel Pax8 monoclonal antibody was used to re-evaluate whether Pax8 was indeed expressed in islets. Surprisingly, Pax8 was not detected in neither the developing pancreas or in mature islets. Reappraisal of pancreatic neuroendocrine tumors using this Pax8 monoclonal antibody exhibited no immunostaining as compared to the Pax8 polyclonal antibody. In conclusion, Pax8 is not expressed in the pancreas and cast doubts on the value of Pax8 as a pancreatic neuroendocrine tumor marker.
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页码:595 / 607
页数:12
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