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Expression of the transcription factor ZBTB46 distinguishes human histiocytic disorders of classical dendritic cell origin
Distinguishing classical dendritic cells from other myeloid cell types is complicated by the shared expression of cell surface markers. ZBTB46 is a zinc finger and BTB domain-containing transcription factor, which is expressed by dendritic cells and committed dendritic cell precursors, but not by pl...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6138663/ https://www.ncbi.nlm.nih.gov/pubmed/29743654 http://dx.doi.org/10.1038/s41379-018-0052-4 |
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author | Satpathy, Ansuman T. Brown, Ryanne A. Gomulia, Ellen Briseno, Carlos G. Mumbach, Maxwell R. Pan, Zenggang Murphy, Kenneth M. Natkunam, Yasodha Chang, Howard Y. Kim, Jinah |
author_facet | Satpathy, Ansuman T. Brown, Ryanne A. Gomulia, Ellen Briseno, Carlos G. Mumbach, Maxwell R. Pan, Zenggang Murphy, Kenneth M. Natkunam, Yasodha Chang, Howard Y. Kim, Jinah |
author_sort | Satpathy, Ansuman T. |
collection | PubMed |
description | Distinguishing classical dendritic cells from other myeloid cell types is complicated by the shared expression of cell surface markers. ZBTB46 is a zinc finger and BTB domain-containing transcription factor, which is expressed by dendritic cells and committed dendritic cell precursors, but not by plasmacytoid dendritic cells, monocytes, macrophages, or other immune cell populations. In this study, we demonstrate that expression of ZBTB46 identifies human dendritic cell neoplasms. We examined ZBTB46 expression in a range of benign and malignant histiocytic disorders and found that ZBTB46 is able to clearly define the dendritic cell identity of many previously unclassified histiocytic disease subtypes. In particular, all examined cases of Langerhans cell histiocytosis and histiocytic sarcoma expressed ZBTB46, while all cases of blastic plasmacytoid dendritic cell neoplasm, chronic myelomonocytic leukemia, juvenile xanthogranuloma, Rosai-Dorfman disease, and Erdheim-Chester disease failed to demonstrate expression of ZBTB46. Moreover, ZBTB46 expression clarified the identity of diagnostically challenging neoplasms, such as cases of indeterminate cell histiocytosis, classifying a fraction of these entities as dendritic cell malignancies. These findings clarify the lineage origins of human histiocytic disorders and distinguish dendritic cell disorders from all other myeloid neoplasms. |
format | Online Article Text |
id | pubmed-6138663 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
record_format | MEDLINE/PubMed |
spelling | pubmed-61386632018-11-09 Expression of the transcription factor ZBTB46 distinguishes human histiocytic disorders of classical dendritic cell origin Satpathy, Ansuman T. Brown, Ryanne A. Gomulia, Ellen Briseno, Carlos G. Mumbach, Maxwell R. Pan, Zenggang Murphy, Kenneth M. Natkunam, Yasodha Chang, Howard Y. Kim, Jinah Mod Pathol Article Distinguishing classical dendritic cells from other myeloid cell types is complicated by the shared expression of cell surface markers. ZBTB46 is a zinc finger and BTB domain-containing transcription factor, which is expressed by dendritic cells and committed dendritic cell precursors, but not by plasmacytoid dendritic cells, monocytes, macrophages, or other immune cell populations. In this study, we demonstrate that expression of ZBTB46 identifies human dendritic cell neoplasms. We examined ZBTB46 expression in a range of benign and malignant histiocytic disorders and found that ZBTB46 is able to clearly define the dendritic cell identity of many previously unclassified histiocytic disease subtypes. In particular, all examined cases of Langerhans cell histiocytosis and histiocytic sarcoma expressed ZBTB46, while all cases of blastic plasmacytoid dendritic cell neoplasm, chronic myelomonocytic leukemia, juvenile xanthogranuloma, Rosai-Dorfman disease, and Erdheim-Chester disease failed to demonstrate expression of ZBTB46. Moreover, ZBTB46 expression clarified the identity of diagnostically challenging neoplasms, such as cases of indeterminate cell histiocytosis, classifying a fraction of these entities as dendritic cell malignancies. These findings clarify the lineage origins of human histiocytic disorders and distinguish dendritic cell disorders from all other myeloid neoplasms. 2018-05-09 2018-09 /pmc/articles/PMC6138663/ /pubmed/29743654 http://dx.doi.org/10.1038/s41379-018-0052-4 Text en Users may view, print, copy, and download text and data-mine the content in such documents, for the purposes of academic research, subject always to the full Conditions of use: http://www.nature.com/authors/editorial_policies/license.html#terms |
spellingShingle | Article Satpathy, Ansuman T. Brown, Ryanne A. Gomulia, Ellen Briseno, Carlos G. Mumbach, Maxwell R. Pan, Zenggang Murphy, Kenneth M. Natkunam, Yasodha Chang, Howard Y. Kim, Jinah Expression of the transcription factor ZBTB46 distinguishes human histiocytic disorders of classical dendritic cell origin |
title | Expression of the transcription factor ZBTB46 distinguishes human histiocytic disorders of classical dendritic cell origin |
title_full | Expression of the transcription factor ZBTB46 distinguishes human histiocytic disorders of classical dendritic cell origin |
title_fullStr | Expression of the transcription factor ZBTB46 distinguishes human histiocytic disorders of classical dendritic cell origin |
title_full_unstemmed | Expression of the transcription factor ZBTB46 distinguishes human histiocytic disorders of classical dendritic cell origin |
title_short | Expression of the transcription factor ZBTB46 distinguishes human histiocytic disorders of classical dendritic cell origin |
title_sort | expression of the transcription factor zbtb46 distinguishes human histiocytic disorders of classical dendritic cell origin |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6138663/ https://www.ncbi.nlm.nih.gov/pubmed/29743654 http://dx.doi.org/10.1038/s41379-018-0052-4 |
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