Ere removed, and the inner side was whipped with cotton swaps and stained with Harris hematoxylin solution (Sigma-Aldrich). After washing, filters were cut out, mounted on microscope slides. Four images covering the majority of the sample were collected from each filter, then cells were counted using ImageJ software. Migrated B cells were counted by flow cytometry. For CFDA-SE labeling (Invitrogen), 56105 B16 tumor-primed B cells were stained with CFSE (0.5 mM, final concentration) for 15 min at 37uC and plated in 2 FBS-RPMI 1640 with or without additional 10 TCM in the transwell chamber. After 24 hrs, B cell migration and proliferation were determined by flow cytometry.RNA Isolation and Quantitative Real-time PCRTotal RNA was extracted using the RNeasy kit (Qiagen) or RNA queous-Micro Scale RNA Isolation kit (Ambion) according to the manufacturer’s instruction. RNA (0.5 to 1 mg) was 58-49-1 reversetranscribed to cDNA using iScript cDNA Synthesis Kit (Bio-Rad), and real-time PCR reactions were performed using iQ SYBR Green supermix (Bio-Rad) on a DNA Engine thermal cycler equipped with Chromo4 detector (Bio-Rad). Gene specific primer sets were purchased from SA Bioscience. The 18S rRNA housekeeping gene was used as an internal control to normalize mRNA DprE1-IN-2 expression.B Cells Induce Endothelial Cell Tube Formation via StatTo further substantiate the importance of B cells with activated Stat3 in stimulating tumor angiogenesis, we performed in vivo Matrigel assays using B cells with or without intact Stat3 signaling. Matrigel plugs containing both tumor cells and Stat3+/+ B cells exhibited markedly increased tumor vascularization in vivo, compared to those with only B16 tumor cells or B cells (Fig. 2A and 2B). Although addition of Stat32/2 B cells to B16 tumor cells increased blood vessel formation somewhat, it was highly significantly less compared to that by adding Stat3+/+ B cells to B16 tumor cells (Fig. 2A, 2B and Figure S2A). Immunofluorescent staining of sections prepared from Matrigel plugs also showed the promoting effect of Stat3+/+ B cells on tumor angiogenesis (Figure S2B). Next, we assessed whether B cells and their intrinsic Stat3 signaling would affect endothelial cells’ ability in forming blood ?vessels. Co-culturing endothelial cells with naive splenic B cells significantly enhanced endothelial cell tube formation, indicating that B cells can upregulate the angiogenic potential of endothelialProtein Preparation and Western Blot AnalysisCells or tissues were lysed in a modified RIPA buffer containing 50 mM Tris, pH 7.4, 1 NP-40, 150 mM NaCl, 1 mM EDTA, 1 mM Na3VO4 and protease inhibitor cocktail (Roche). Tissue lysates were prepared by FastPrep homogenizor (MP Biomedicals). The lysates were clarified by centrifugation, and protein concentrations were determined by Bio-Rad protein assay. Equivalent amounts of total cellular proteins were separated by SDS plus 8?15 PAGE according to protein molecular weight, transferred onto nitrocellulose membranes, probed with the respective antibodies, and detected for signals using horseradish peroxiSTAT3-High B Cells Crucial for Tumor AngiogenesisFigure 1. B cells with activated Stat3 accelerate tumor progression and increase blood vessel formation in tumors. (A and B) Left, Growth curve of B16 (A) or LLC (B) tumors in Rag12/2 mice, without or with Stat3+/+or Stat32/2 B cells. B cells were enriched from splenocytes of B16 or LLC tumor-bearing mice with or without Stat3 ablated in hematopoietic c.Ere removed, and the inner side was whipped with cotton swaps and stained with Harris hematoxylin solution (Sigma-Aldrich). After washing, filters were cut out, mounted on microscope slides. Four images covering the majority of the sample were collected from each filter, then cells were counted using ImageJ software. Migrated B cells were counted by flow cytometry. For CFDA-SE labeling (Invitrogen), 56105 B16 tumor-primed B cells were stained with CFSE (0.5 mM, final concentration) for 15 min at 37uC and plated in 2 FBS-RPMI 1640 with or without additional 10 TCM in the transwell chamber. After 24 hrs, B cell migration and proliferation were determined by flow cytometry.RNA Isolation and Quantitative Real-time PCRTotal RNA was extracted using the RNeasy kit (Qiagen) or RNA queous-Micro Scale RNA Isolation kit (Ambion) according to the manufacturer’s instruction. RNA (0.5 to 1 mg) was reversetranscribed to cDNA using iScript cDNA Synthesis Kit (Bio-Rad), and real-time PCR reactions were performed using iQ SYBR Green supermix (Bio-Rad) on a DNA Engine thermal cycler equipped with Chromo4 detector (Bio-Rad). Gene specific primer sets were purchased from SA Bioscience. The 18S rRNA housekeeping gene was used as an internal control to normalize mRNA expression.B Cells Induce Endothelial Cell Tube Formation via StatTo further substantiate the importance of B cells with activated Stat3 in stimulating tumor angiogenesis, we performed in vivo Matrigel assays using B cells with or without intact Stat3 signaling. Matrigel plugs containing both tumor cells and Stat3+/+ B cells exhibited markedly increased tumor vascularization in vivo, compared to those with only B16 tumor cells or B cells (Fig. 2A and 2B). Although addition of Stat32/2 B cells to B16 tumor cells increased blood vessel formation somewhat, it was highly significantly less compared to that by adding Stat3+/+ B cells to B16 tumor cells (Fig. 2A, 2B and Figure S2A). Immunofluorescent staining of sections prepared from Matrigel plugs also showed the promoting effect of Stat3+/+ B cells on tumor angiogenesis (Figure S2B). Next, we assessed whether B cells and their intrinsic Stat3 signaling would affect endothelial cells’ ability in forming blood ?vessels. Co-culturing endothelial cells with naive splenic B cells significantly enhanced endothelial cell tube formation, indicating that B cells can upregulate the angiogenic potential of endothelialProtein Preparation and Western Blot AnalysisCells or tissues were lysed in a modified RIPA buffer containing 50 mM Tris, pH 7.4, 1 NP-40, 150 mM NaCl, 1 mM EDTA, 1 mM Na3VO4 and protease inhibitor cocktail (Roche). Tissue lysates were prepared by FastPrep homogenizor (MP Biomedicals). The lysates were clarified by centrifugation, and protein concentrations were determined by Bio-Rad protein assay. Equivalent amounts of total cellular proteins were separated by SDS plus 8?15 PAGE according to protein molecular weight, transferred onto nitrocellulose membranes, probed with the respective antibodies, and detected for signals using horseradish peroxiSTAT3-High B Cells Crucial for Tumor AngiogenesisFigure 1. B cells with activated Stat3 accelerate tumor progression and increase blood vessel formation in tumors. (A and B) Left, Growth curve of B16 (A) or LLC (B) tumors in Rag12/2 mice, without or with Stat3+/+or Stat32/2 B cells. B cells were enriched from splenocytes of B16 or LLC tumor-bearing mice with or without Stat3 ablated in hematopoietic c.