Figure 2.
Skin, immune cell, and serum Ig changes in MYD88L265Pmice. (A) Representative gross pathology photographs of submandibular skin showing dermatitis and alopecia in MYD88L265P but not MYD88WT mice. (B) H&E, Giemsa, and IHC stains of indicated cell markers on serial submandibular skin sections from representative MYD88WT and MYD88L265P mice. Giemsa stain was used to identify mast cells; F4/80, macrophages. Scale bars: white, 10 µm; black, 100 µm. Percentage of T cells (C), macrophages (D), and mast cells (E) or number of mast cells relative to the tissue area (F) per field in the submandibular skin of MYD88WT and MYD88L265P mice. Measurements were made with inForm Cell Analysis Software analyzing 8 fields per genotype. Graphs depict the mean ± SD. P values were calculated by using Welch’s t test. (G) Histologic (H&E) analysis of representative cervical LNs demonstrating cyst development in MYD88L265P but not in AIDCre or MYD88WT mice. Scale bars: white, 50 µm; black, 500 µm. Representative density plots (H) and graphs (I) depicting the mean ± SD of flow cytometric analysis of splenic lymphoid cell subpopulations from AIDCre (n = 6), MYD88WT (n = 7), and MYD88L265P (n = 6) mice immunized with SRBCs. (J) Serum Ig concentrations assessed using multiplex immunoassay in MYD88L265P mice grouped according to severity of submandibular skin lesions. Graphs depict the median ± 25th to 75th percentile. P values were calculated by using Mann-Whitney U test. (K) Percentage of MYD88L265P mice classified by the severity of submandibular skin lesions with serum IL-6 concentrations >49 pg/mL assessed using multiplex immunoassay. P value was calculated by using Fisher’s exact test. (L) IHC stains of indicated cytokines on serial submandibular skin sections from representative MYD88WT and MYD88L265P mice. Scale bars: white, 10 µm; black, 100 µm.

Skin, immune cell, and serum Ig changes in MYD88L265Pmice. (A) Representative gross pathology photographs of submandibular skin showing dermatitis and alopecia in MYD88L265P but not MYD88WT mice. (B) H&E, Giemsa, and IHC stains of indicated cell markers on serial submandibular skin sections from representative MYD88WT and MYD88L265P mice. Giemsa stain was used to identify mast cells; F4/80, macrophages. Scale bars: white, 10 µm; black, 100 µm. Percentage of T cells (C), macrophages (D), and mast cells (E) or number of mast cells relative to the tissue area (F) per field in the submandibular skin of MYD88WT and MYD88L265P mice. Measurements were made with inForm Cell Analysis Software analyzing 8 fields per genotype. Graphs depict the mean ± SD. P values were calculated by using Welch’s t test. (G) Histologic (H&E) analysis of representative cervical LNs demonstrating cyst development in MYD88L265P but not in AIDCre or MYD88WT mice. Scale bars: white, 50 µm; black, 500 µm. Representative density plots (H) and graphs (I) depicting the mean ± SD of flow cytometric analysis of splenic lymphoid cell subpopulations from AIDCre (n = 6), MYD88WT (n = 7), and MYD88L265P (n = 6) mice immunized with SRBCs. (J) Serum Ig concentrations assessed using multiplex immunoassay in MYD88L265P mice grouped according to severity of submandibular skin lesions. Graphs depict the median ± 25th to 75th percentile. P values were calculated by using Mann-Whitney U test. (K) Percentage of MYD88L265P mice classified by the severity of submandibular skin lesions with serum IL-6 concentrations >49 pg/mL assessed using multiplex immunoassay. P value was calculated by using Fisher’s exact test. (L) IHC stains of indicated cytokines on serial submandibular skin sections from representative MYD88WT and MYD88L265P mice. Scale bars: white, 10 µm; black, 100 µm.

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