| Literature DB >> 32207982 |
Shivanthan Shanthikumar1,2,3, Matthew Burton4, Richard Saffery5,6, Sarath C Ranganathan7,2,6, Melanie R Neeland8,6.
Abstract
Childhood pulmonary diseases not only cause childhood morbidity and mortality, but can also cause long term pulmonary impairment. The clinical management of many childhood pulmonary diseases is hampered by a limited understanding of the underlying pathophysiological mechanisms. Flow cytometry, which can be used to phenotype individual cell populations or isolate cells for downstream analysis, represents a crucial technology which can help to elucidate the pathophysiology of these conditions. Here, we describe a flow cytometry-based method for purification and characterisation of cell populations in bronchoalveolar lavage (BAL) from children. This includes assessment of the effect of cryopreservation on cell phenotype and frequency, a knowledge gap recently identified by an American Thoracic Society report on flow cytometry in lung samples. To our knowledge, this is the first study to simultaneously quantify alveolar macrophages, T cells (CD4 and CD8), B cells, NK cells, dendritic cells, granulocytes and monocytes (CD16+/CD16-) in the BAL of children. The protocols described can be used to advance investigation of the pathophysiology of childhood pulmonary diseases.Entities:
Keywords: Bronchoalveolar Lavage; Cryopreservation; Flow Cytometry; Pediatrics; cystic fibrosis
Year: 2020 PMID: 32207982 DOI: 10.1165/rcmb.2019-0453MA
Source DB: PubMed Journal: Am J Respir Cell Mol Biol ISSN: 1044-1549 Impact factor: 6.914