Journal: International Journal of Molecular Sciences

Article Title: Regenerative Effects of Hypoxia Primed Flowable Placental Formulation in Muscle and Dermal Injury

doi: 10.3390/ijms22137151

Figure Lengend Snippet: Angiogenic and anti-inflammatory response in FPF-treated wounds. ( A ) Neovascularization in control (left panel) and FPF treated (right panel) tissue samples collected after wound closure was determined by αSMA (top panel, stained green) and CD31 (middle panel, stained red). Merged images (bottom panel) show the colocalization of αSMA and CD31. Nuclei were counterstained with DAPI (blue). White arrows indicate αSMA- and CD31-positive blood vessels. Graphs represent the vessel density and size distribution of αSMA and CD31positive blood vessels. Scale bar = 50 μm. N = 6 for saline; N = 9 for FPF group. Inflammatory cell staining was determined by ( B ) MPO (red) staining for neutrophils. Scale bar = 50 μm and ( C ) CD163 (red) staining for M2 macrophages. Scale bar = 50 μm. Nuclei were counterstained with DAPI (blue). N = 6/group. * p < 0.05, ** p < 0.01, *** p < 0.005.

Article Snippet: The following primary antibodies and concentrations were used: for α smooth muscle actin (αSMA), rabbit polyclonal anti-αSMA primary antibody for 45 min (0.33 μg/mL) (#ab5694, Abcam, Waltham, MA, USA); for CD31, mouse monoclonal (TLD-3A12) anti-CD31 primary antibody for 45 min (10 μg/mL) (#MA1-80069, Invitrogen, Waltham, MA, USA); for CD68, mouse monoclonal (ED-1) anti-CD68 primary antibody for 30 min (5 μg/mL) (#MCA341, Biorad, Hercules, CA, USA); for CD163, mouse monoclonal (ED-2) anti-CD163 primary antibody for 30 min (6.67 μg/mL) (#MCA342, Biorad, Hercules, CA, USA); for collagen IV, rabbit polyclonal anti-collagen IV primary antibody for 60 min (10 μg/mL) (Invitrogen #PA1-28534); for MPO, rabbit polyclonal anti-MPO primary antibody for 30 min (1.33 μg/mL) (#ab9535, Abcam, Waltham, MA, USA).

Techniques: Control, Staining, Saline

Journal: Veterinary Research

Article Title: Distribution of porcine monocytes in different lymphoid tissues and the lungs during experimental Actinobacillus pleuropneumoniae infection and the role of chemokines

doi: 10.1186/1297-9716-44-98

Figure Lengend Snippet: Overview of flow cytometry analyses. (A) Gating strategy for identification of monocytes and macrophages. The peripheral blood is shown. Designation of population shown within each dot-plot is indicated above the dot-plot. Leukocytes were identified as viable (a) non-doublet (b) cells with typical light scatter properties of leukocytes (c) . Then, macrophages were gated simply as CD203a hi leukocytes (d) and marked with blue color. Monocytes were gated as CD203a low/- SWC8 - (e) CD172a hi (f) leukocytes where the CD203a low/- region was defined as the complementary region to the CD203a hi region. Then, SLA-DR + monocytes were marked with red color and SLA-DR - monocytes were marked with green color (g) . SLA-DR - region was defined as the complementary region to the SLA-DR + region. Gating order is shown in the scheme (h) . (B) Representative CD163 vs. CD14 dot-plots of macrophages (blue) and monocyte subpopulations (green: SLA-DR – , red: SLA-DR + ) in various body compartments of control and APP-infected pigs.

Article Snippet: BM and PB mononuclear cells, freshly isolated from BM and PB samples by Lympholyte-H gradient (Cedarlane, Burlington, Canada) centrifugation at 800 g , were labeled with anti-CD163 antibody for 15 min at 4 °C.

Techniques: Flow Cytometry, Infection

Journal: Veterinary Research

Article Title: Distribution of porcine monocytes in different lymphoid tissues and the lungs during experimental Actinobacillus pleuropneumoniae infection and the role of chemokines

doi: 10.1186/1297-9716-44-98

Figure Lengend Snippet: Primers for chemokines, chemokine receptors, CD62L and reference gene used in quantitative real-time PCR.

Article Snippet: BM and PB mononuclear cells, freshly isolated from BM and PB samples by Lympholyte-H gradient (Cedarlane, Burlington, Canada) centrifugation at 800 g , were labeled with anti-CD163 antibody for 15 min at 4 °C.

Techniques:

Journal: Veterinary Research

Article Title: Distribution of porcine monocytes in different lymphoid tissues and the lungs during experimental Actinobacillus pleuropneumoniae infection and the role of chemokines

doi: 10.1186/1297-9716-44-98

Figure Lengend Snippet: Monocyte subpopulations in various body compartments from control and APP-infected pigs.

Article Snippet: BM and PB mononuclear cells, freshly isolated from BM and PB samples by Lympholyte-H gradient (Cedarlane, Burlington, Canada) centrifugation at 800 g , were labeled with anti-CD163 antibody for 15 min at 4 °C.

Techniques:

Journal: Veterinary Research

Article Title: Distribution of porcine monocytes in different lymphoid tissues and the lungs during experimental Actinobacillus pleuropneumoniae infection and the role of chemokines

doi: 10.1186/1297-9716-44-98

Figure Lengend Snippet: Representative pictures of immunohistochemical detection of CD163 + cells in tracheobronchial lymph node and spleen. CD163 + cells were detected in tracheobronchial lymph nodes from control (A) and APP-infected pigs (B) and in spleen from control (C) and APP-infected pigs (D) . Immunohistochemical visualization: horseradish peroxidase, brown substrate, hematoxylin counterstain; c, cortex; ca, central artery; e, ellipsoid; f, follicle; mz, marginal zone; pals, periarterial lymphatic sheath, rp, red pulp; s, subcapsular sinus.

Article Snippet: BM and PB mononuclear cells, freshly isolated from BM and PB samples by Lympholyte-H gradient (Cedarlane, Burlington, Canada) centrifugation at 800 g , were labeled with anti-CD163 antibody for 15 min at 4 °C.

Techniques: Immunohistochemical staining, Infection

Journal: Veterinary Research

Article Title: Distribution of porcine monocytes in different lymphoid tissues and the lungs during experimental Actinobacillus pleuropneumoniae infection and the role of chemokines

doi: 10.1186/1297-9716-44-98

Figure Lengend Snippet: Intensity of CD163, CD14 and SLA-DR expression by CD14 + /CD163 + monocytes in various body compartments. Data are shown as MFI (Median of fluorescence intensity) ± S.E.M. BM, bone marrow ( n = 5); PB, peripheral blood ( n = 5), UA, lungs-unaffected area ( n = 5), DZ, lungs-demarcation zone ( n = 4), NA, lungs-necrotic area ( n = 5), TBLN, tracheobronchial lymph node ( n = 5); MLN, mesenteric lymph node ( n = 4), spleen ( n = 4). The significant differences (Kruskal-Wallis test) amongst particular compartments are indicated.

Article Snippet: BM and PB mononuclear cells, freshly isolated from BM and PB samples by Lympholyte-H gradient (Cedarlane, Burlington, Canada) centrifugation at 800 g , were labeled with anti-CD163 antibody for 15 min at 4 °C.

Techniques: Expressing, Fluorescence

Journal: Veterinary Research

Article Title: Distribution of porcine monocytes in different lymphoid tissues and the lungs during experimental Actinobacillus pleuropneumoniae infection and the role of chemokines

doi: 10.1186/1297-9716-44-98

Figure Lengend Snippet: Chemokine receptor, CD62L, CD163 and TBP1 expression by bone marrow and peripheral blood CD163 + monocytes from control and APP-infected pigs.

Article Snippet: BM and PB mononuclear cells, freshly isolated from BM and PB samples by Lympholyte-H gradient (Cedarlane, Burlington, Canada) centrifugation at 800 g , were labeled with anti-CD163 antibody for 15 min at 4 °C.

Techniques: Expressing

Journal: Veterinary Research

Article Title: Distribution of porcine monocytes in different lymphoid tissues and the lungs during experimental Actinobacillus pleuropneumoniae infection and the role of chemokines

doi: 10.1186/1297-9716-44-98

Figure Lengend Snippet: Chemokine receptor, CD62L and CD163 expression in lungs from control and APP-infected pigs.

Article Snippet: BM and PB mononuclear cells, freshly isolated from BM and PB samples by Lympholyte-H gradient (Cedarlane, Burlington, Canada) centrifugation at 800 g , were labeled with anti-CD163 antibody for 15 min at 4 °C.

Techniques: Expressing

Journal: Veterinary Research

Article Title: Distribution of porcine monocytes in different lymphoid tissues and the lungs during experimental Actinobacillus pleuropneumoniae infection and the role of chemokines

doi: 10.1186/1297-9716-44-98

Figure Lengend Snippet: Scheme of chemokines and corresponding chemokine receptor mRNA expression in various organs and CD163 + monocytes. Chemokines in bone marrow, necrotic area of the lungs and tracheobronchial lymph nodes and chemokine receptors in necrotic areas of the lungs and tracheobronchial lymph nodes which were up-regulated in the APP-infected pigs compared to control are highlighted in bold. Chemokine receptors in bone marrow and peripheral blood CD163 + monocytes which were expressed at relatively lower levels are highlighted in bold. Those expressed in relatively high levels are highlighted in bold and underlined. Arrangement of the scheme was created based on the review of Bonecchi et al. .

Article Snippet: BM and PB mononuclear cells, freshly isolated from BM and PB samples by Lympholyte-H gradient (Cedarlane, Burlington, Canada) centrifugation at 800 g , were labeled with anti-CD163 antibody for 15 min at 4 °C.

Techniques: Expressing, Infection

Journal: World Journal of Surgical Oncology

Article Title: A study of the correlation between M2 macrophages and lymph node metastasis of colorectal carcinoma

doi: 10.1186/s12957-021-02195-5

Figure Lengend Snippet: Expression of M2 macrophages in lymph nodes. Detection of CD163 in lymph nodes of colorectal carcinoma patients by immunohistochemistry. The membrane and cytoplasm of M2 macrophages are stained brown. Microscopic analysis of a typical example of CD163 expression in non-metastatic lymph nodes ( a , b , c magnification × 100, × 200, × 400, respectively). d , e Location of CD163 in metastatic lymph node tissue at a magnification of × 200 and × 400 respectively. M2 macrophages are seen mainly infiltrating into the tumor stroma

Article Snippet: The tissue sections were incubated with an endogenous peroxidase blocker at room temperature for 10 min, blocked with 3% goat serum (cat. No. KIT-9710; Maixin-Bio, Fuzhou, China) for 30 min, rinsed with phosphate-buffered saline (PBS), incubated with ready-to-use mouse anti-human CD163 monoclonal antibody (cat. No. MAB-0206; Maixin-Bio) at room temperature for 60 min, followed by sequential addition of biotin-labeled IgG polymer and streptavidin peroxidase (cat. No. KIT-9710; Maixin-Bio).

Techniques: Expressing, Immunohistochemistry, Staining

Journal: International Journal of Nanomedicine

Article Title: A Macrophages-Enriched Head and Neck Tumor Spheroid Model to Study Foslip ® Behavior in Tumor Microenvironment

doi: 10.2147/IJN.S427350

Figure Lengend Snippet: Characterization of M0 macrophage polarization into M1 and M2 macrophages. ( A ) CD68 and CD163 macrophage staining by immunohistochemistry. Scale bar 10 µm. ( B ) Surface expression of CD80, CD163 and CD206 by flow cytometry analysis. Data were normalized to M0r conditions. ( C ) Gene expression of macrophages after incubation with Tumor-, M1-, and M2-conditioned media were assessed using RT-qPCR. The data were normalized to the M0r conditions. * p <0.05; *** p < 0.001 using ANOVA analysis with Tukey’s corrections.

Article Snippet: Immunological staining of CD68 (a marker for total macrophage population) and CD163 markers was performed using the Dako Omnis IHC automate (Dako Agilent, Santa Clara, US) with mouse anti-human CD68 (clone KP1, Dako Omnis Santa Clara, US) and mouse anti-human CD163 (clone 10D6, Clinisciences, Nanterre, France).

Techniques: Staining, Immunohistochemistry, Expressing, Flow Cytometry, Incubation, Quantitative RT-PCR