دورية أكاديمية

The Lymphangioleiomyomatosis Lung Cell and Its Human Cell Models

التفاصيل البيبلوغرافية
العنوان: The Lymphangioleiomyomatosis Lung Cell and Its Human Cell Models
المؤلفون: Steagall, Wendy K, Pacheco-Rodriguez, Gustavo, Darling, Thomas N, Torre, Olga, Harari, Sergio, Moss, Joel
المساهمون: W.K. Steagall, G. Pacheco-Rodriguez, T.N. Darling, O. Torre, S. Harari, J. Moss
سنة النشر: 2018
المجموعة: The University of Milan: Archivio Istituzionale della Ricerca (AIR)
مصطلحات موضوعية: TSC2, loss of heterozygosity, lymphangioleiomyomatosi, tuberous sclerosi, Female, Gene Expression Regulation, Neoplastic, Human, Lung Neoplasm, Mutation, Skin, Tumor Cells, Cultured, Settore MED/11 - Malattie dell'Apparato Cardiovascolare
الوصف: Lymphangioleiomyomatosis (LAM) is a multisystem disease of women, affecting lungs, kidneys, and lymphatics. It is caused by the proliferation of abnormal smooth muscle-like LAM cells, with mutations and loss of heterozygosity in the TSC1 or, more frequently, TSC2 genes. Isolated pulmonary LAM cells have been difficult to maintain in culture, and most studies of LAM lung cells involve mixtures of TSC2 wild-type and TSC2-null cells. A clonal population of LAM lung cells has not been established, making analysis of the cells challenging. Cell lines have been established from angiomyolipomas, a common manifestation of LAM, and from tumors from patients with TSC. Circulating LAM cells have also been isolated from blood and other body fluids. LAM cells may also be identified in clusters apparently derived from lymphatic vessels. Genetics, patterns of antigen expression, and signaling pathways have been studied in LAM lung tissue and in LAM cell models, although rarely all in the same study. We show here that LAM cells manifest differences in these characteristics, depending on the source investigated, suggesting further studies.
نوع الوثيقة: article in journal/newspaper
اللغة: English
العلاقة: info:eu-repo/semantics/altIdentifier/pmid/29406787; info:eu-repo/semantics/altIdentifier/wos/WOS:000433972100005; volume:58; issue:6; firstpage:678; lastpage:683; numberofpages:6; journal:AMERICAN JOURNAL OF RESPIRATORY CELL AND MOLECULAR BIOLOGY; http://hdl.handle.net/2434/748541Test; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-85048227924
DOI: 10.1165/rcmb.2017-0403TR
الإتاحة: https://doi.org/10.1165/rcmb.2017-0403TRTest
http://hdl.handle.net/2434/748541Test
حقوق: info:eu-repo/semantics/openAccess
رقم الانضمام: edsbas.2D232C92
قاعدة البيانات: BASE