tetano
Editor, Senior Moderator
Am J Physiol Lung Cell Mol Physiol
. 2024 Jan 30.
doi: 10.1152/ajplung.00236.2023. Online ahead of print. Aryl hydrocarbon receptor activation alters immune cell populations in the lung and bone marrow during coronavirus infection
Alicia M Healey[SUP] 1 [/SUP], Kristina N Fenner[SUP] 2 [/SUP], Colleen T O'Dell[SUP] 3 [/SUP], B Paige Lawrence[SUP] 2 [/SUP]
Affiliations
Respiratory viral infections are one of the major causes of illness and death worldwide. Symptoms associated with respiratory infections can range from mild to severe, and there is limited understanding of why there is large variation in severity. Environmental exposures are a potential causative factor. The aryl hydrocarbon receptor (AHR) is an environment sensing molecule expressed in all immune cells. While there is considerable evidence that AHR signaling influences immune responses to other immune challenges, including respiratory pathogens, less is known about the impact of AHR signaling on immune responses during coronavirus (CoV) infection. In this study, we report that AHR activation significantly altered immune cells in the lungs and bone marrow of mice infected with a mouse coronavirus. AHR activation transiently reduced the frequency of multiple cells in the mononuclear phagocyte system, including monocytes, interstitial macrophages, and dendritic cells in the lung. In the bone marrow, AHR activation altered myelopoiesis, as evidenced by a reduction in granulocyte-monocyte progenitor cells and an increased frequency of myeloid-biased progenitor cells. Moreover, AHR activation significantly affected multiple stages of the megakaryocyte lineage. Overall, these findings indicate that AHR activation modulates multiple aspects of the immune response to a CoV infection. Given the significant burden of respiratory viruses on human health, understanding how environmental exposures shape immune responses to infection advances our knowledge of factors that contribute to variability in disease severity and provides insight into novel approaches to prevent or treat disease.
Keywords: Respiratory virus infection; emergency hematopoiesis; environmental exposure; hematopoietic stem and progenitor cells; myeloid cells.
. 2024 Jan 30.
doi: 10.1152/ajplung.00236.2023. Online ahead of print. Aryl hydrocarbon receptor activation alters immune cell populations in the lung and bone marrow during coronavirus infection
Alicia M Healey[SUP] 1 [/SUP], Kristina N Fenner[SUP] 2 [/SUP], Colleen T O'Dell[SUP] 3 [/SUP], B Paige Lawrence[SUP] 2 [/SUP]
Affiliations
- PMID: 38290163
- DOI: 10.1152/ajplung.00236.2023
Respiratory viral infections are one of the major causes of illness and death worldwide. Symptoms associated with respiratory infections can range from mild to severe, and there is limited understanding of why there is large variation in severity. Environmental exposures are a potential causative factor. The aryl hydrocarbon receptor (AHR) is an environment sensing molecule expressed in all immune cells. While there is considerable evidence that AHR signaling influences immune responses to other immune challenges, including respiratory pathogens, less is known about the impact of AHR signaling on immune responses during coronavirus (CoV) infection. In this study, we report that AHR activation significantly altered immune cells in the lungs and bone marrow of mice infected with a mouse coronavirus. AHR activation transiently reduced the frequency of multiple cells in the mononuclear phagocyte system, including monocytes, interstitial macrophages, and dendritic cells in the lung. In the bone marrow, AHR activation altered myelopoiesis, as evidenced by a reduction in granulocyte-monocyte progenitor cells and an increased frequency of myeloid-biased progenitor cells. Moreover, AHR activation significantly affected multiple stages of the megakaryocyte lineage. Overall, these findings indicate that AHR activation modulates multiple aspects of the immune response to a CoV infection. Given the significant burden of respiratory viruses on human health, understanding how environmental exposures shape immune responses to infection advances our knowledge of factors that contribute to variability in disease severity and provides insight into novel approaches to prevent or treat disease.
Keywords: Respiratory virus infection; emergency hematopoiesis; environmental exposure; hematopoietic stem and progenitor cells; myeloid cells.