Is remained at the vehicle control level.DiscussionAngiogenesis in the lung

Is remained at the vehicle control level.DiscussionGulated and 25 probesets (16 genes) were downregulated in the high CINGEC group. angiogenesis in the lung is triggered by inflammatory conditions and specifically by up-regulation of the CXC chemokines [3,22?25]. Their pro-angiogenic effect has been demonstrated in many studies [26?8] and work from our laboratory has shown that the cytokine CXCL2 and its high-affinity receptor CXCR2 are involved in the overall process of bronchial angiogenesis following pulmonary ischemia. This past study demonstrated an increase in total lung CXCL2 within the first day after the onset of ischemia and an inhibitory effect of anti-CXCR2 on bronchial angiogenesis [12,29]. Yet the localization within the lung and the temporal regulation of the CXC chemokines that lead to bronchial arteriogenesis are unknown. Moreover, it is unclear how lung parenchymal growth factors can activate upstream bronchial angiogenesis. Thus, the present study was designed to examine the early expression of CXC chemokines following pulmonary ischemia (0?4 h), specifically focusing on the timing and local expression of CXCL1 and CXCL2 in BAL fluid and airway tissue. Additionally, we studied the effectiveness of anti-inflammatory therapy in limiting local cytokine levels (BAL and airway tissue), and to correlate this effect with the magnitude of bronchial angiogenesis. Our data demonstrate the presence of bothNegative modulation of the inflammatory response is not sufficient to reduce bronchial angiogenesisTo determine if dexamethasone affected bronchial neovascularization after pulmonary ischemia, we measured proliferative status of bronchial vascular endothelium early (3 d, n = 3? lungs/ group) and functional neovascularization later (14 d n = 4?/ group) after LPAL. Figure 7A shows a representative image (2006 original magnification) of an airway wall showing bronchial vessels and associated positive PCNA staining. An average of 2563 airways/lung were studied which were associated with an average of 205620 bronchial vessels that were evaluated for bronchial endothelial cell proliferation. Control lungs represent left lungs from rats undergoing sham surgery (thoracotomy with no LPAL) and since they did not differ, were grouped with the right lungs of sham and LPAL rats. LPAL caused a significant increase in the fraction of PCNA+ vessels (P,0.008, Figure 7B). Treatment of rats with dexamethasone had no significant effect on the fraction of proliferating bronchial vessels Title Loaded From File assessed 3 d after LPAL (p.0.05 LPAL vs LPAL + dex). Functional blood vesselsAcute Ischemia and CXC ChemokinesFigure 4. CXCL1 and CXCL2 cytokines mRNA (A, B), protein levels in the left bronchus (C), and (D) frozen section of left bronchus 6 h after LPAL with double staining for CXCL2 (red) and the epithelial cell marker Epcam (green;1006 original magnification and inset: 6006original magnification). CXCL1 (A) and CXCL2 (B) mRNA and CXCL1 and CXCL2 protein levels (C) increased at 6 h LPAL (*P,0.05) and returned to baseline by 24 h LPAL (3? rats/time point). Co-localization of stain for epithelial cells (Epcam,;green) and anti-CXCL2 (red) suggest the airway epithelium is a prominent source for CXCL2. doi:10.1371/journal.pone.0066432.gFigure 5. CXCR1(A) and CXCR2 (B) mRNA in left and right bronchi, and (C) co-localization of CXCR2 with RECA-1+ subepithelial blood vessel. Significant changes in CXCR2 were measured only in the left bronchus (*P,0.05 from 0 h and ##P,0.01 from right bronchus). Frozen sections of left bronchus 6 h after LPAL show co-l.Is remained at the vehicle control level.DiscussionAngiogenesis in the lung is triggered by inflammatory conditions and specifically by up-regulation of the CXC chemokines [3,22?25]. Their pro-angiogenic effect has been demonstrated in many studies [26?8] and work from our laboratory has shown that the cytokine CXCL2 and its high-affinity receptor CXCR2 are involved in the overall process of bronchial angiogenesis following pulmonary ischemia. This past study demonstrated an increase in total lung CXCL2 within the first day after the onset of ischemia and an inhibitory effect of anti-CXCR2 on bronchial angiogenesis [12,29]. Yet the localization within the lung and the temporal regulation of the CXC chemokines that lead to bronchial arteriogenesis are unknown. Moreover, it is unclear how lung parenchymal growth factors can activate upstream bronchial angiogenesis. Thus, the present study was designed to examine the early expression of CXC chemokines following pulmonary ischemia (0?4 h), specifically focusing on the timing and local expression of CXCL1 and CXCL2 in BAL fluid and airway tissue. Additionally, we studied the effectiveness of anti-inflammatory therapy in limiting local cytokine levels (BAL and airway tissue), and to correlate this effect with the magnitude of bronchial angiogenesis. Our data demonstrate the presence of bothNegative modulation of the inflammatory response is not sufficient to reduce bronchial angiogenesisTo determine if dexamethasone affected bronchial neovascularization after pulmonary ischemia, we measured proliferative status of bronchial vascular endothelium early (3 d, n = 3? lungs/ group) and functional neovascularization later (14 d n = 4?/ group) after LPAL. Figure 7A shows a representative image (2006 original magnification) of an airway wall showing bronchial vessels and associated positive PCNA staining. An average of 2563 airways/lung were studied which were associated with an average of 205620 bronchial vessels that were evaluated for bronchial endothelial cell proliferation. Control lungs represent left lungs from rats undergoing sham surgery (thoracotomy with no LPAL) and since they did not differ, were grouped with the right lungs of sham and LPAL rats. LPAL caused a significant increase in the fraction of PCNA+ vessels (P,0.008, Figure 7B). Treatment of rats with dexamethasone had no significant effect on the fraction of proliferating bronchial vessels assessed 3 d after LPAL (p.0.05 LPAL vs LPAL + dex). Functional blood vesselsAcute Ischemia and CXC ChemokinesFigure 4. CXCL1 and CXCL2 cytokines mRNA (A, B), protein levels in the left bronchus (C), and (D) frozen section of left bronchus 6 h after LPAL with double staining for CXCL2 (red) and the epithelial cell marker Epcam (green;1006 original magnification and inset: 6006original magnification). CXCL1 (A) and CXCL2 (B) mRNA and CXCL1 and CXCL2 protein levels (C) increased at 6 h LPAL (*P,0.05) and returned to baseline by 24 h LPAL (3? rats/time point). Co-localization of stain for epithelial cells (Epcam,;green) and anti-CXCL2 (red) suggest the airway epithelium is a prominent source for CXCL2. doi:10.1371/journal.pone.0066432.gFigure 5. CXCR1(A) and CXCR2 (B) mRNA in left and right bronchi, and (C) co-localization of CXCR2 with RECA-1+ subepithelial blood vessel. Significant changes in CXCR2 were measured only in the left bronchus (*P,0.05 from 0 h and ##P,0.01 from right bronchus). Frozen sections of left bronchus 6 h after LPAL show co-l.