pβCD induce alveolar
macrophage depletion and pulmonary apoptosis.
(A) BALB/c mice received one i.n. administration of pβCD (150
mg/mL, 50 μL) and were euthanized at indicated time points postadministration
to evaluate the number of different cell populations in lungs by flow
cytometry. The following cell types were analyzed: alveolar macrophages
(CD11c+ F4/80+ SiglecF+), interstitial
macrophages (F4/80+ CD11cint SiglecF–), neutrophils (CD11b+ LY6G+), eosinophils
(SiglecF+ CD11c–), T cells (CD3+), and B cells (B220+ MHCII+). (B) BALB/c mice
were inoculated via the i.n. route with Mtb H37Rv
(105 CFU). At days 7, 9, 11, 14, 16, and 18 postchallenge,
mice received administrations of 50 μL of pβCD (150 mg/mL) via the e.t. route. At day 21 postchallenge, 50 μL
of NucView 488 caspase-3 substrate (diluted in PBS) was administered
i.n. to each mouse for 1 h before lung harvesting and subsequent fluorescence
histology analysis. Data are presented as mean ± SEM and are
representative of two independent experiments. Symbols *, **, and
*** denote p < 0.05, p < 0.01,
and p < 0.001, respectively.