2022
DOI: 10.14715/cmb/2022.68.6.18
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Effects of Netrin-1 and NHE1 Participation on the Migration of Macrophages Driven by CCL2

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Cited by 3 publications
(4 citation statements)
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“…In this study, firstly, through cytological experiment, we verified that β2-AR, β2-AR stimulant on the surface of macrophages can not only promote the conversion of macrophages to M2 type but also inhibit the conversion of macrophages to M1 type (24), and confirmed that β-AR blockers with different degrees of blocking effect on β2-AR, including metoprolol, propranolol and ICI118551, are agonists that can regulate the polarization state of macrophages in the opposite way to that of β2-AR stimulant salbutamol through β2-AR (25)(26)(27). The β2-AR stimulant or the β-AR blocker performs mutual reverse intervention of promotion or inhibition on the process that ox-LDL promotes the M2 type differentiation of macrophages, further verifying that ox-LDL can promote the M2 type differentiation of macrophages (18)(19)(20), and further verifies that M2 type macrophages are more sensitive to lipid toxicity than M1-type macrophages (19,28). However, its phagocytic ability is stronger than that of M1-type macrophages (7), and it is more likely to form foam cells (19,29).…”
Section: Discussionmentioning
confidence: 83%
See 1 more Smart Citation
“…In this study, firstly, through cytological experiment, we verified that β2-AR, β2-AR stimulant on the surface of macrophages can not only promote the conversion of macrophages to M2 type but also inhibit the conversion of macrophages to M1 type (24), and confirmed that β-AR blockers with different degrees of blocking effect on β2-AR, including metoprolol, propranolol and ICI118551, are agonists that can regulate the polarization state of macrophages in the opposite way to that of β2-AR stimulant salbutamol through β2-AR (25)(26)(27). The β2-AR stimulant or the β-AR blocker performs mutual reverse intervention of promotion or inhibition on the process that ox-LDL promotes the M2 type differentiation of macrophages, further verifying that ox-LDL can promote the M2 type differentiation of macrophages (18)(19)(20), and further verifies that M2 type macrophages are more sensitive to lipid toxicity than M1-type macrophages (19,28). However, its phagocytic ability is stronger than that of M1-type macrophages (7), and it is more likely to form foam cells (19,29).…”
Section: Discussionmentioning
confidence: 83%
“…However, its phagocytic ability is stronger than that of M1-type macrophages (7), and it is more likely to form foam cells (19,29). M2type macrophages that engulf ox-LDL are more likely to die than other forms of macrophages (19,28). The in-depth study on the mode of death of macrophages after consuming ox-LDL has revealed that, in addition to apoptosis, non-apoptotic modes of death such as pyroptosis, in which the cell membrane is ruptured, are also included.…”
Section: Discussionmentioning
confidence: 99%
“…Previous studies indicated that the subtype of NHE1 acts an important role in cell migration 15 . Inhibition or knockout of NHE1 can inhibit macrophage and breast cancer cell migration 38,39 . Thus, in order to determine the role of the expression modification of NHE1 in 1,25(OH) 2 D 3 ameliorating cell migration, we employed qRT‐PCR to measure the transcript level of NHE1.…”
Section: Resultsmentioning
confidence: 99%
“…15 Inhibition or knockout of NHE1 can inhibit macrophage and breast cancer cell migration. 38,39 Thus, in order to determine the role of the expression modification of NHE1 in 1,25 (OH) 2 D 3 ameliorating cell migration, we employed qRT-PCR to measure the transcript level of NHE1. As revealed in Figure 4A, the transcript level of NHE1 in LLC cells was predominately down-regulated after the 24 h treatment of 1,25(OH) 2 D 3 (100 nM).…”
Section: 25(oh) 2 D 3 Inhibited Activity and Expression Of Nhe1mentioning
confidence: 99%