AI Article Synopsis

  • - MSR1, a receptor typically found in macrophages, shows significantly increased expression in peripheral blood mononuclear cells (PBMCs) of asthmatic patients, indicating its potential involvement in these conditions.
  • - The study analyzed PBMCs from healthy individuals and patients with asthma and COPD, confirming higher MSR1 expression through methods like RT-qPCR and flow cytometry.
  • - MSR1 was detected on various immune cell types, particularly B lymphocytes and monocytes, with expression levels varying based on disease type and severity, highlighting its potential role in asthma and COPD.

Article Abstract

Background: Macrophage scavenger receptor 1 (MSR1) has mostly been described in macrophages, but we previously found a significant gene expression increase in peripheral blood mononuclear cells (PBMCs) of asthmatic patients.

Objective: To confirm those results and to define its cellular origin in PBMCs.

Methods: Four groups of subjects were studied: healthy controls (C), nonallergic asthmatic (NA), allergic asthmatic (AA), and chronic obstructive pulmonary disease (COPD) patients. RNA was extracted from PBMCs. MSR1 gene expression was analyzed by RT-qPCR. The presence of MSR1 on the cellular surface of PBMC cellular subtypes was analyzed by confocal microscopy and flow cytometry.

Results: MSR1 gene expression was significantly increased in the three clinical conditions compared to the healthy control group, with substantial variations according to disease type and severity. MSR1 expression on T cells (CD4 and CD8), B cells, and monocytes was confirmed by confocal microscopy and flow cytometry. In all clinical groups, the four immune cell subtypes studied expressed MSR1, with a greater expression on B lymphocytes and monocytes, exhibiting differences according to disease and severity.

Conclusions: This is the first description of MSR1's presence on lymphocytes' surfaces and reinforces the potential role of MSR1 as a player in asthma and COPD.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC8910889PMC
http://dx.doi.org/10.3390/jcm11051439DOI Listing

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