Fig. 6.
Fig. 6. Immunohistochemical demonstration of the presence of inflammatory cells in muscles of WT and Plg-deficient mice after glycerol-induced injury. / Detection of neutrophils (Gr-1+) (A), macrophages (Mac-1+) (B), and T cells (T11+) (C) in transverse sections of control and injured skeletal muscles of WT and Plg-deficient mice at the indicated times AI. (D) Quantitative analysis of Gr-1+, Mac-1+, and T11+ cells in regenerating muscles of WT and Plg-deficient mice. Gr-1+, Mac-1+, and T11+ cells were counted in 10 random fields per section, and data from 12 sections per muscle were pooled. The mean values for both limbs were to provide a mean value for each animal (3 animals were studied at each time point). Histograms show the percentage of reduction of Mac-1+ and T11+ cells (50% and 30%, respectively) in Plg−/− mice (gray bars) with respect to WT mice (black bars); statistical significant (P < .05) is denoted. Gr-1–expressing cells were maximal 12 hours AI in both WT and Plg-deficient mice. Mac-1– and T11-expressing cells increased 2 days AI in muscle of WT and Plg-deficient mice; however, the number of Mac-1+ and T11+ cells was lower in Plg−/− mouse muscle. Original magnifications × 400.

Immunohistochemical demonstration of the presence of inflammatory cells in muscles of WT and Plg-deficient mice after glycerol-induced injury.

Detection of neutrophils (Gr-1+) (A), macrophages (Mac-1+) (B), and T cells (T11+) (C) in transverse sections of control and injured skeletal muscles of WT and Plg-deficient mice at the indicated times AI. (D) Quantitative analysis of Gr-1+, Mac-1+, and T11+ cells in regenerating muscles of WT and Plg-deficient mice. Gr-1+, Mac-1+, and T11+ cells were counted in 10 random fields per section, and data from 12 sections per muscle were pooled. The mean values for both limbs were to provide a mean value for each animal (3 animals were studied at each time point). Histograms show the percentage of reduction of Mac-1+ and T11+ cells (50% and 30%, respectively) in Plg−/− mice (gray bars) with respect to WT mice (black bars); statistical significant (P < .05) is denoted. Gr-1–expressing cells were maximal 12 hours AI in both WT and Plg-deficient mice. Mac-1– and T11-expressing cells increased 2 days AI in muscle of WT and Plg-deficient mice; however, the number of Mac-1+ and T11+ cells was lower in Plg−/− mouse muscle. Original magnifications × 400.

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