 Macrophages, Alveolar
"Macrophages, Alveolar" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus,
MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure,
which enables searching at various levels of specificity.
Round, granular, mononuclear phagocytes found in the alveoli of the lungs. They ingest small inhaled particles resulting in degradation and presentation of the antigen to immunocompetent cells.
| Descriptor ID |
D016676
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| MeSH Number(s) |
A11.329.372.600 A11.627.482.600 A11.733.397.600 A15.382.680.397.600 A15.382.812.522.600
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| Concept/Terms |
Macrophages, Alveolar- Macrophages, Alveolar
- Macrophages, Pulmonary
- Macrophage, Pulmonary
- Alveolar Macrophages
- Alveolar Macrophage
- Macrophage, Alveolar
- Pulmonary Macrophage
- Pulmonary Macrophages
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Below are MeSH descriptors whose meaning is more general than "Macrophages, Alveolar".
Below are MeSH descriptors whose meaning is more specific than "Macrophages, Alveolar".
This graph shows the total number of publications written about "Macrophages, Alveolar" by people in UAMS Profiles by year, and whether "Macrophages, Alveolar" was a major or minor topic of these publications.
To see the data from this visualization as text, click here.
| Year | Major Topic | Minor Topic | Total |
|---|
| 2022 | 1 | 0 | 1 | | 2021 | 2 | 1 | 3 | | 2020 | 1 | 0 | 1 | | 2019 | 0 | 1 | 1 | | 2018 | 1 | 0 | 1 | | 2013 | 1 | 0 | 1 | | 2012 | 2 | 0 | 2 | | 2007 | 1 | 0 | 1 | | 2003 | 0 | 1 | 1 | | 2002 | 1 | 0 | 1 | | 1998 | 1 | 0 | 1 | | 1994 | 0 | 1 | 1 |
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Below are the most recent publications written about "Macrophages, Alveolar" by people in Profiles over the past ten years.
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Andrews JT, Voth DE, Huang SC, Huang L. Breathe In, Breathe Out: Metabolic Regulation of Lung Macrophages in Host Defense Against Bacterial Infection. Front Cell Infect Microbiol. 2022; 12:934460.
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Puzyrenko A, Jacobs ER, Sun Y, Felix JC, Sheinin Y, Ge L, Lai S, Dai Q, Gantner BN, Nanchal R, North PE, Simpson PM, Rui H, Benjamin IJ. Pneumocytes are distinguished by highly elevated expression of the ER stress biomarker GRP78, a co-receptor for SARS-CoV-2, in COVID-19 autopsies. Cell Stress Chaperones. 2021 09; 26(5):859-868.
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Pisu D, Huang L, Narang V, Theriault M, L?-Bury G, Lee B, Lakudzala AE, Mzinza DT, Mhango DV, Mitini-Nkhoma SC, Jambo KC, Singhal A, Mwandumba HC, Russell DG. Single cell analysis of M. tuberculosis phenotype and macrophage lineages in the infected lung. J Exp Med. 2021 09 06; 218(9).
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Dragan AL, Voth DE. Take my breath away: studying pathogen invasion of the human lung using primary tissue models. Pathog Dis. 2021 03 31; 79(4).
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Xu-Vanpala S, Deerhake ME, Wheaton JD, Parker ME, Juvvadi PR, MacIver N, Ciofani M, Shinohara ML. Functional heterogeneity of alveolar macrophage population based on expression of CXCL2. Sci Immunol. 2020 08 07; 5(50).
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Banerjee SK, Huckuntod SD, Mills SD, Kurten RC, Pechous RD. Modeling Pneumonic Plague in Human Precision-Cut Lung Slices Highlights a Role for the Plasminogen Activator Protease in Facilitating Type 3 Secretion. Infect Immun. 2019 08; 87(8).
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Huang L, Nazarova EV, Tan S, Liu Y, Russell DG. Growth of Mycobacterium tuberculosis in vivo segregates with host macrophage metabolism and ontogeny. J Exp Med. 2018 04 02; 215(4):1135-1152.
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Miller M, Esnault S, Kurten RC, Kelly EA, Beppu A, Das S, Rosenthal P, Ramsdell J, Croft M, Zuraw B, Jarjour N, Hamid Q, Broide DH. Segmental allergen challenge increases levels of airway follistatin-like 1 in patients with asthma. J Allergy Clin Immunol. 2016 08; 138(2):596-599.e4.
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