Human Alveolar and Splenic Macrophage Populations Display a Distinct Transcriptomic Response to Infection With Mycobacterium tuberculosis

Front Immunol. 2020 Apr 21:11:630. doi: 10.3389/fimmu.2020.00630. eCollection 2020.

Abstract

Mycobacterium tuberculosis (Mtb) infects alveolar macrophages (AMs), causing pulmonary tuberculosis (PTB), the most common form of the disease. Less frequently, Mtb is disseminated to many other organs and tissues, resulting in different extrapulmonary forms of TB. Nevertheless, very few studies have addressed the global mRNA response of human AMs, particularly from humans with the active form of the disease. Strikingly, almost no studies have addressed the response of human extrapulmonary macrophages to Mtb infection. In this pilot study, using microarray technology, we examined the transcriptomic ex vivo response of AMs from PTB patients (AMTBs) and AMs from control subjects (AMCTs) infected with two clinical isolates of Mtb. Furthermore, we also studied the infection response of human splenic macrophages (SMs) to Mtb isolates, as a model for extrapulmonary infection, and compared the transcriptomic response between AMs and SMs. Our results showed a striking difference in global mRNA profiles in response to infection between AMs and SMs, implicating a tissue-specific macrophage response to Mtb.

Keywords: M. tuberculosis; clinical isolates; human alveolar macrophages; microarray; splenic macrophages; transcriptome.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Case-Control Studies
  • Female
  • Gene Expression Profiling / methods
  • Gene Regulatory Networks
  • Host Microbial Interactions / genetics
  • Humans
  • Macrophages, Alveolar / immunology*
  • Male
  • Middle Aged
  • Mycobacterium tuberculosis / immunology*
  • Pilot Projects
  • RNA, Messenger / genetics
  • Spleen / immunology*
  • Spleen / pathology
  • Transcriptome*
  • Tuberculosis, Pulmonary / immunology*
  • Tuberculosis, Pulmonary / microbiology
  • Young Adult

Substances

  • RNA, Messenger