التفاصيل البيبلوغرافية
| العنوان: |
DataSheet_1_Role of CCR2+ Myeloid Cells in Inflammation Responses Driven by Expression of a Surfactant Protein-C Mutant in the Alveolar Epithelium.pdf |
| المؤلفون: |
Alessandro Venosa (10686315), Sophie Cowman (6553691), Jeremy Katzen (10686318), Yaniv Tomer (10686321), Brittnie S. Armstrong (10686324), Surafel Mulugeta (1373886), Michael F. Beers (10686327) |
| سنة النشر: |
2021 |
| المجموعة: |
Smithsonian Institution: Digital Repository |
| مصطلحات موضوعية: |
Immunology, Applied Immunology (incl. Antibody Engineering, Xenotransplantation and T-cell Therapies), Autoimmunity, Cellular Immunology, Humoural Immunology and Immunochemistry, Immunogenetics (incl. Genetic Immunology), Innate Immunity, Transplantation Immunology, Tumour Immunology, Immunology not elsewhere classified, Genetic Immunology, Animal Immunology, Veterinary Immunology, alveolar type-2 cell, Sftpc I73T surfactant protein-C I73T mutant, idiopathic pulmonary fibrosis, chemokine receptor-2, monocyte-derived alveolar macrophages, acute exacerbation of PF |
| الوصف: |
Acute inflammatory exacerbations (AIE) represent precipitous deteriorations of a number of chronic lung conditions, including pulmonary fibrosis (PF), chronic obstructive pulmonary disease and asthma. AIEs are marked by diffuse and persistent polycellular alveolitis that profoundly accelerate lung function decline and mortality. In particular, excess monocyte mobilization during AIE and their persistence in the lung have been linked to poor disease outcome. The etiology of AIEs remains quite uncertain, but environmental exposure and genetic predisposition/mutations have been identified as two contributing factors. Guided by clinical evidence, we have developed a mutant model of pulmonary fibrosis leveraging the PF-linked missense isoleucine to threonine substitution at position 73 [I73T] in the alveolar type-2 cell-restricted Surfactant Protein-C [SP-C] gene [SFTPC]. With this toolbox at hand, the present work investigates the role of peripheral monocytes during the initiation and progression of AIE-PF. Genetic ablation of CCR2 + monocytes (SP-C I73T CCR2 KO ) resulted in improved lung histology, mouse survival, and reduced inflammation compared to SP-C I73T CCR2 WT cohorts. FACS analysis of CD11b + CD64 - Ly6C hi monocytes isolated 3 d and 14 d after SP-C I73T induced injury reveals dynamic transcriptional changes associated with “Innate Immunity’ and ‘Extracellular Matrix Organization’ signaling. While immunohistochemical and in situ hybridization analysis revealed comparable levels of tgfb1 mRNA expression localized primarily in parenchymal cells found nearby foci of injury we found reduced effector cell activation (C1q, iNOS, Arg1) in SP-C I73T CCR2 KO lungs as well as partial colocalization of tgfb1 mRNA expression in Arg1 + cells. These results provide a detailed picture of the role of resident macrophages and recruited monocytes in the context of AIE-PF driven by alveolar epithelial dysfunction. |
| نوع الوثيقة: |
dataset |
| اللغة: |
unknown |
| Relation: |
https://figshare.com/articles/dataset/DataSheet_1_Role_of_CCR2_Myeloid_Cells_in_Inflammation_Responses_Driven_by_Expression_of_a_Surfactant_Protein-C_Mutant_in_the_Alveolar_Epithelium_pdf/14465817 |
| DOI: |
10.3389/fimmu.2021.665818.s001 |
| الاتاحة: |
https://doi.org/10.3389/fimmu.2021.665818.s001 |
| Rights: |
CC BY 4.0 |
| رقم الانضمام: |
edsbas.F23C148B |
| قاعدة البيانات: |
BASE |