دورية أكاديمية

Macrophage Ontogeny Underlies Differences in Tumor-Specific Education in Brain Malignancies.

التفاصيل البيبلوغرافية
العنوان: Macrophage Ontogeny Underlies Differences in Tumor-Specific Education in Brain Malignancies.
المؤلفون: Bowman, R.L., Klemm, F., Akkari, L., Pyonteck, S.M., Sevenich, L., Quail, D.F., Dhara, S., Simpson, K., Gardner, E.E., Iacobuzio-Donahue, C.A., Brennan, C.W., Tabar, V., Gutin, P.H., Joyce, J.A.
المصدر: Cell reports, vol. 17, no. 9, pp. 2445-2459
سنة النشر: 2016
المجموعة: Université de Lausanne (UNIL): Serval - Serveur académique lausannois
مصطلحات موضوعية: Animals, Base Sequence, Bone Marrow Cells/pathology, Brain Neoplasms/genetics, Brain Neoplasms/pathology, Cell Lineage, Disease Models, Animal, Gene Expression Regulation, Neoplastic, Gene Regulatory Networks, Glioma/genetics, Glioma/pathology, Humans, Integrin alpha4/metabolism, Macrophage Activation, Macrophages/metabolism, Macrophages/pathology, Mice, Microglia/metabolism, Microglia/pathology, Sequence Analysis, RNA, Transcription Factors/metabolism, CD49D, Macrophage, brain metastasis, glioma, microglia, tumor-associated macrophages
الوصف: Extensive transcriptional and ontogenetic diversity exists among normal tissue-resident macrophages, with unique transcriptional profiles endowing the cells with tissue-specific functions. However, it is unknown whether the origins of different macrophage populations affect their roles in malignancy. Given potential artifacts associated with irradiation-based lineage tracing, it remains unclear if bone-marrow-derived macrophages (BMDMs) are present in tumors of the brain, a tissue with no homeostatic involvement of BMDMs. Here, we employed multiple models of murine brain malignancy and genetic lineage tracing to demonstrate that BMDMs are abundant in primary and metastatic brain tumors. Our data indicate that distinct transcriptional networks in brain-resident microglia and recruited BMDMs are associated with tumor-mediated education yet are also influenced by chromatin landscapes established before tumor initiation. Furthermore, we demonstrate that microglia specifically repress Itga4 (CD49D), enabling its utility as a discriminatory marker between microglia and BMDMs in primary and metastatic disease in mouse and human.
نوع الوثيقة: article in journal/newspaper
وصف الملف: application/pdf
اللغة: English
العلاقة: info:eu-repo/semantics/altIdentifier/pmid/27840052; info:eu-repo/semantics/altIdentifier/eissn/2211-1247; info:eu-repo/semantics/altIdentifier/urn/urn:nbn:ch:serval-BIB_D0474EC65CDA8; https://serval.unil.ch/notice/serval:BIB_D0474EC65CDATest; https://serval.unil.ch/resource/serval:BIB_D0474EC65CDA.P003/REF.pdfTest; http://nbn-resolving.org/urn/resolver.pl?urn=urn:nbn:ch:serval-BIB_D0474EC65CDA8Test
DOI: 10.1016/j.celrep.2016.10.052
الإتاحة: https://doi.org/10.1016/j.celrep.2016.10.052Test
https://serval.unil.ch/notice/serval:BIB_D0474EC65CDATest
https://serval.unil.ch/resource/serval:BIB_D0474EC65CDA.P003/REF.pdfTest
http://nbn-resolving.org/urn/resolver.pl?urn=urn:nbn:ch:serval-BIB_D0474EC65CDA8Test
حقوق: info:eu-repo/semantics/openAccess ; Copying allowed only for non-profit organizations ; https://serval.unil.ch/disclaimerTest
رقم الانضمام: edsbas.21386A48
قاعدة البيانات: BASE