mortality/aging
• in a model of pneumococcal pneumonia, exhibit 100% lethality compared to 40% in wild-type
|
immune system
• microarchitecture of the spleen marginal zone is altered
• marginal zones have fewer numbers of SIGNR1+ cells that do not tightly adhere to each other resulting in a gap between the marginal zone and the sinus
|
• alveolar macrophages exhibit impaired in vitro binding of Streptococcus pneumoniae
|
• alveolar macrophages exhibit impaired in vivo uptake of unopsonized particles
|
• homozygous mice treated with the inert environmental particle TiO2 show enhanced inflammation and chemokine expression compared to wild-type
|
• in a model of pneumococcal pneumonia, homozygotes show an impaired ability to clear bacteria from the lungs, increased pulmonary inflammation and cytokine release, and diminished survival
(J:115081)
• following immunization with pneumoccocal bacterial serotype, mice have a decreased anti-polysaccharide IgM response
(J:122271)
|
hematopoietic system
• microarchitecture of the spleen marginal zone is altered
• marginal zones have fewer numbers of SIGNR1+ cells that do not tightly adhere to each other resulting in a gap between the marginal zone and the sinus
|
• alveolar macrophages exhibit impaired in vitro binding of Streptococcus pneumoniae
|
• alveolar macrophages exhibit impaired in vivo uptake of unopsonized particles
|
cellular
• alveolar macrophages exhibit impaired in vivo uptake of unopsonized particles
|