Hil infiltration was 1 day, and a low number of neutrophils were observed 14 days after pSNL surgery. Because the reduction of neutrophil infiltration by TRPM2 deficiency wasobserved only 8 h after pSNL surgery [24], it is possible that the reduction was not detected at 14 days after the surgery in the present study, although it has not been determined whether Iba1?GFP+ peripheral immune cells, particularly Gr-1+ neutrophils, are reduced in TRPM2-KO BM chimeric mice 8 h after pSNL surgery.TRPM2 in Spinal Infiltration of Macrophage in PainTable 2. The numbers of Iba1+ and 15481974 target=’resource_window’>10457188 GFP+ cells in the spinal dorsal horn.Contralateral Donor (BM) Total cells Iba1 cells GFP+ cells Iba1?GFP+ cells Iba1+/GFP?cells Iba1+/GFP+ cells+Ipsilateral TRPMBM?Rec+TRPMBM+/Rec+TRPMBM+/Rec?TRPMBM?Rec?TRPM2BM+/Rec+ TRPM2BM?Rec+ TRPM2BM+/Rec?TRPM2BM?Rec?41.0 6 4.6 39.0 6 3.6 32.7 6 5.5 2.0 6 1.0 8.3 6 1.8 30.7 6 4.6 25.0 6 10.1 20.0 6 7.9 15.0 6 10.0 5.0 6 5.0 10.0 6 5.5 10.0 6 5.5* 24.3 6 1.5 20.0 6 2.0 19.4 6 3.2 4.2 6 1.8 4.8 6 2.6 15.2 6 2.3* 23.8 6 5.8 20.2 6 5.7 13.3 6 2.6 3.7 6 1.1 10.5 6 3.7 9.7 6 2.7**3.7 6 0.7 3.0 6 0.0 1.0 6 1.0 0.7 6 0.7 2.7 6 0.3 0.3 6 0.4.0 6 2.0 3.3 6 1.9 1.0 6 0.6 0.7 6 0.3 3.0 6 2.1 0.3 6 0.5.0 6 0.4 3.6 6 0.9 2.6 6 0.2 1.4 6 0.5 2.4 6 0.6 1.2 6 0.5.2 6 1.7 3.8 6 1.4 2.0 6 0.8 1.3 6 0.5 3.2 6 1.1 0.7 6 0.The numbers of Iba1+ cells, GFP+ cells, Iba1+/GFP?cells, Iba1?GFP+ cells, and Iba1+/GFP+ cells were counted in the contralateral and ipsilateral spinal dorsal horn 14 days after pSNL surgery. “Total cells” indicates the sum of Iba1+/GFP?cells, Iba1?GFP+ cells, and Iba1+/GFP+ cells. n = 3?. Data are expressed as mean 6 SEM. doi:10.1371/journal.pone.0066410.tBy contrast, the number of Iba1+ cells in the spinal dorsal horn tended to decrease in all TRPM2-KO chimeric mice 14 days after pSNL surgery. However, the number of GFP?Iba1+ cells, representing spinal-resident microglia, was not ML 240 site changed in any TRPM2-KO chimeric mice. These findings suggest that the increased number of Iba1+ cells in the spinal dorsal horn is mainly due to the increase in the spinal infiltration of Iba1+ Licochalcone A cost macrophages, and that TRPM2 plays no role in the increased number of spinalresident microglia, at least at 14 days after pSNL surgery. Notably, the increased number of GFP?Iba1+ resident microglia represents an increase in microglial proliferation and/or chemotaxis from other regions, rather than microglial activation. The activation of spinal microglia (represented by an increase in Iba1 immunoreactivity and morphological changes to activation state) peaks at 3 days and declines within 2 weeks after pSNL surgery [24], while spinal infiltration of peripheral immune cells is delayed following the activation of spinal-resident microglia. Spinal infiltration by peripheral immune cells starts at 3 days and peaks at 14 days after peripheral nerve injury [6,35]. Our previous report demonstrated that TRPM2 plays a critical role in the initial activation of spinalresident microglia [24]. The present results showed that the number of GFP+ cells in the spinal dorsal horn, which represent infiltrated peripheral immune cells, tended to decrease in all TRPM2 chimeric mice. Furthermore, most infiltrated GFP+ peripheral immune cells are Iba1+ macrophages, which were markedly decreased in TRPM2 chimeric mice. Consistent with the present results, recent evidence suggests that peripheral nerve injury induces the infiltration of peripheral immune cells into the spinal cord [4?]. The.Hil infiltration was 1 day, and a low number of neutrophils were observed 14 days after pSNL surgery. Because the reduction of neutrophil infiltration by TRPM2 deficiency wasobserved only 8 h after pSNL surgery [24], it is possible that the reduction was not detected at 14 days after the surgery in the present study, although it has not been determined whether Iba1?GFP+ peripheral immune cells, particularly Gr-1+ neutrophils, are reduced in TRPM2-KO BM chimeric mice 8 h after pSNL surgery.TRPM2 in Spinal Infiltration of Macrophage in PainTable 2. The numbers of Iba1+ and 15481974 target=’resource_window’>10457188 GFP+ cells in the spinal dorsal horn.Contralateral Donor (BM) Total cells Iba1 cells GFP+ cells Iba1?GFP+ cells Iba1+/GFP?cells Iba1+/GFP+ cells+Ipsilateral TRPMBM?Rec+TRPMBM+/Rec+TRPMBM+/Rec?TRPMBM?Rec?TRPM2BM+/Rec+ TRPM2BM?Rec+ TRPM2BM+/Rec?TRPM2BM?Rec?41.0 6 4.6 39.0 6 3.6 32.7 6 5.5 2.0 6 1.0 8.3 6 1.8 30.7 6 4.6 25.0 6 10.1 20.0 6 7.9 15.0 6 10.0 5.0 6 5.0 10.0 6 5.5 10.0 6 5.5* 24.3 6 1.5 20.0 6 2.0 19.4 6 3.2 4.2 6 1.8 4.8 6 2.6 15.2 6 2.3* 23.8 6 5.8 20.2 6 5.7 13.3 6 2.6 3.7 6 1.1 10.5 6 3.7 9.7 6 2.7**3.7 6 0.7 3.0 6 0.0 1.0 6 1.0 0.7 6 0.7 2.7 6 0.3 0.3 6 0.4.0 6 2.0 3.3 6 1.9 1.0 6 0.6 0.7 6 0.3 3.0 6 2.1 0.3 6 0.5.0 6 0.4 3.6 6 0.9 2.6 6 0.2 1.4 6 0.5 2.4 6 0.6 1.2 6 0.5.2 6 1.7 3.8 6 1.4 2.0 6 0.8 1.3 6 0.5 3.2 6 1.1 0.7 6 0.The numbers of Iba1+ cells, GFP+ cells, Iba1+/GFP?cells, Iba1?GFP+ cells, and Iba1+/GFP+ cells were counted in the contralateral and ipsilateral spinal dorsal horn 14 days after pSNL surgery. “Total cells” indicates the sum of Iba1+/GFP?cells, Iba1?GFP+ cells, and Iba1+/GFP+ cells. n = 3?. Data are expressed as mean 6 SEM. doi:10.1371/journal.pone.0066410.tBy contrast, the number of Iba1+ cells in the spinal dorsal horn tended to decrease in all TRPM2-KO chimeric mice 14 days after pSNL surgery. However, the number of GFP?Iba1+ cells, representing spinal-resident microglia, was not changed in any TRPM2-KO chimeric mice. These findings suggest that the increased number of Iba1+ cells in the spinal dorsal horn is mainly due to the increase in the spinal infiltration of Iba1+ macrophages, and that TRPM2 plays no role in the increased number of spinalresident microglia, at least at 14 days after pSNL surgery. Notably, the increased number of GFP?Iba1+ resident microglia represents an increase in microglial proliferation and/or chemotaxis from other regions, rather than microglial activation. The activation of spinal microglia (represented by an increase in Iba1 immunoreactivity and morphological changes to activation state) peaks at 3 days and declines within 2 weeks after pSNL surgery [24], while spinal infiltration of peripheral immune cells is delayed following the activation of spinal-resident microglia. Spinal infiltration by peripheral immune cells starts at 3 days and peaks at 14 days after peripheral nerve injury [6,35]. Our previous report demonstrated that TRPM2 plays a critical role in the initial activation of spinalresident microglia [24]. The present results showed that the number of GFP+ cells in the spinal dorsal horn, which represent infiltrated peripheral immune cells, tended to decrease in all TRPM2 chimeric mice. Furthermore, most infiltrated GFP+ peripheral immune cells are Iba1+ macrophages, which were markedly decreased in TRPM2 chimeric mice. Consistent with the present results, recent evidence suggests that peripheral nerve injury induces the infiltration of peripheral immune cells into the spinal cord [4?]. The.
