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Mouse Il 6 Elisa Kit, supplied by R&D Systems, used in various techniques. Bioz Stars score: 94/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Mouse Il 6 Elisa Kit, supplied by Elabscience Biotechnology, used in various techniques. Bioz Stars score: 95/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Cusabio il 6
OM-MSCs-Exo induced M2-polarized microglial cells through FGFR1 delivery, resulting in attenuated neuronal inflammation. A CCK8 assay in HT-22 and SH-SY5Y cells. B The apoptosis rate of HT-22 and SH-SY5Y cells was analyzed by flow cytometry. C IL-1β, TNF-α, <t>and</t> <t>IL-6</t> levels of HT-22 and SH-SY5Y cells. The HT-22 cells in the Co-control group, Co-Aβ 1–42 group, Co-Aβ 1–42 + OM-MSCs-Exo group, Co-Aβ 1–42 + OM-MSCs-Exo oe−NC group, and Co-Aβ 1–42 + OM-MSCs-Exo oe−FGFR1 group were co-cultured with the corresponding BV2 cells for 24 h. The SH-SY5Y cells in the Co-control group, Co-Aβ 1–42 group, Co-Aβ 1–42 + OM-MSCs-Exo group, Co-Aβ 1–42 + OM-MSCs-Exo oe−NC group, and Co-Aβ 1–42 + OM-MSCs-Exo oe−FGFR1 group were co-cultured with the corresponding HMC3 cells for 24 h ( n = 3). * p < 0.05, ** p < 0.01, *** p < 0.001. Normality was confirmed using the Shapiro–Wilk test. Thereafter, data were analyzed with a one-way ANOVA (followed by Tukey’s post hoc test) for multiple-group comparisons
Il 6, supplied by Cusabio, used in various techniques. Bioz Stars score: 96/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Boster Bio il 6
OM-MSCs-Exo induced M2-polarized microglial cells through FGFR1 delivery, resulting in attenuated neuronal inflammation. A CCK8 assay in HT-22 and SH-SY5Y cells. B The apoptosis rate of HT-22 and SH-SY5Y cells was analyzed by flow cytometry. C IL-1β, TNF-α, <t>and</t> <t>IL-6</t> levels of HT-22 and SH-SY5Y cells. The HT-22 cells in the Co-control group, Co-Aβ 1–42 group, Co-Aβ 1–42 + OM-MSCs-Exo group, Co-Aβ 1–42 + OM-MSCs-Exo oe−NC group, and Co-Aβ 1–42 + OM-MSCs-Exo oe−FGFR1 group were co-cultured with the corresponding BV2 cells for 24 h. The SH-SY5Y cells in the Co-control group, Co-Aβ 1–42 group, Co-Aβ 1–42 + OM-MSCs-Exo group, Co-Aβ 1–42 + OM-MSCs-Exo oe−NC group, and Co-Aβ 1–42 + OM-MSCs-Exo oe−FGFR1 group were co-cultured with the corresponding HMC3 cells for 24 h ( n = 3). * p < 0.05, ** p < 0.01, *** p < 0.001. Normality was confirmed using the Shapiro–Wilk test. Thereafter, data were analyzed with a one-way ANOVA (followed by Tukey’s post hoc test) for multiple-group comparisons
Il 6, supplied by Boster Bio, used in various techniques. Bioz Stars score: 96/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Cedarlane il 6 concentration
OM-MSCs-Exo induced M2-polarized microglial cells through FGFR1 delivery, resulting in attenuated neuronal inflammation. A CCK8 assay in HT-22 and SH-SY5Y cells. B The apoptosis rate of HT-22 and SH-SY5Y cells was analyzed by flow cytometry. C IL-1β, TNF-α, <t>and</t> <t>IL-6</t> levels of HT-22 and SH-SY5Y cells. The HT-22 cells in the Co-control group, Co-Aβ 1–42 group, Co-Aβ 1–42 + OM-MSCs-Exo group, Co-Aβ 1–42 + OM-MSCs-Exo oe−NC group, and Co-Aβ 1–42 + OM-MSCs-Exo oe−FGFR1 group were co-cultured with the corresponding BV2 cells for 24 h. The SH-SY5Y cells in the Co-control group, Co-Aβ 1–42 group, Co-Aβ 1–42 + OM-MSCs-Exo group, Co-Aβ 1–42 + OM-MSCs-Exo oe−NC group, and Co-Aβ 1–42 + OM-MSCs-Exo oe−FGFR1 group were co-cultured with the corresponding HMC3 cells for 24 h ( n = 3). * p < 0.05, ** p < 0.01, *** p < 0.001. Normality was confirmed using the Shapiro–Wilk test. Thereafter, data were analyzed with a one-way ANOVA (followed by Tukey’s post hoc test) for multiple-group comparisons
Il 6 Concentration, supplied by Cedarlane, used in various techniques. Bioz Stars score: 92/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Image Search Results


OM-MSCs-Exo induced M2-polarized microglial cells through FGFR1 delivery, resulting in attenuated neuronal inflammation. A CCK8 assay in HT-22 and SH-SY5Y cells. B The apoptosis rate of HT-22 and SH-SY5Y cells was analyzed by flow cytometry. C IL-1β, TNF-α, and IL-6 levels of HT-22 and SH-SY5Y cells. The HT-22 cells in the Co-control group, Co-Aβ 1–42 group, Co-Aβ 1–42 + OM-MSCs-Exo group, Co-Aβ 1–42 + OM-MSCs-Exo oe−NC group, and Co-Aβ 1–42 + OM-MSCs-Exo oe−FGFR1 group were co-cultured with the corresponding BV2 cells for 24 h. The SH-SY5Y cells in the Co-control group, Co-Aβ 1–42 group, Co-Aβ 1–42 + OM-MSCs-Exo group, Co-Aβ 1–42 + OM-MSCs-Exo oe−NC group, and Co-Aβ 1–42 + OM-MSCs-Exo oe−FGFR1 group were co-cultured with the corresponding HMC3 cells for 24 h ( n = 3). * p < 0.05, ** p < 0.01, *** p < 0.001. Normality was confirmed using the Shapiro–Wilk test. Thereafter, data were analyzed with a one-way ANOVA (followed by Tukey’s post hoc test) for multiple-group comparisons

Journal: Molecular Neurobiology

Article Title: Olfactory Mucosa Mesenchymal Stem Cell–Derived Exosomes Enhance Microglia M2 Polarization via the FGFR1/PLCγ1 Axis to Alleviate Alzheimer’s Disease

doi: 10.1007/s12035-026-05797-w

Figure Lengend Snippet: OM-MSCs-Exo induced M2-polarized microglial cells through FGFR1 delivery, resulting in attenuated neuronal inflammation. A CCK8 assay in HT-22 and SH-SY5Y cells. B The apoptosis rate of HT-22 and SH-SY5Y cells was analyzed by flow cytometry. C IL-1β, TNF-α, and IL-6 levels of HT-22 and SH-SY5Y cells. The HT-22 cells in the Co-control group, Co-Aβ 1–42 group, Co-Aβ 1–42 + OM-MSCs-Exo group, Co-Aβ 1–42 + OM-MSCs-Exo oe−NC group, and Co-Aβ 1–42 + OM-MSCs-Exo oe−FGFR1 group were co-cultured with the corresponding BV2 cells for 24 h. The SH-SY5Y cells in the Co-control group, Co-Aβ 1–42 group, Co-Aβ 1–42 + OM-MSCs-Exo group, Co-Aβ 1–42 + OM-MSCs-Exo oe−NC group, and Co-Aβ 1–42 + OM-MSCs-Exo oe−FGFR1 group were co-cultured with the corresponding HMC3 cells for 24 h ( n = 3). * p < 0.05, ** p < 0.01, *** p < 0.001. Normality was confirmed using the Shapiro–Wilk test. Thereafter, data were analyzed with a one-way ANOVA (followed by Tukey’s post hoc test) for multiple-group comparisons

Article Snippet: According to the instruction manuals of the mouse interleukin (IL)−1β (CSB-E08054m; Cusabio), tumor necrosis factor (TNF)-α (CSB-E04741m; Cusabio), IL-6 (CSB-E04639m; Cusabio), and Aβ 1–42 (CSB-E10787m; Cusabio) detection kits, the corresponding molecular levels in cells or tissues were measured.

Techniques: CCK-8 Assay, Flow Cytometry, Control, Cell Culture

OM-MSCs-Exo delivered FGFR1 to interact with PLCγ1 in microglia, suppressing the inflammatory response of co-cultured HT-22 and SH-SY5Y cells. A CCK8 assay in HT-22 and SH-SY5Y cells. B The apoptosis rate of neurons cells was analyzed by flow cytometry. C IL-1β, TNF-α, and IL-6 levels of HT-22 and SH-SY5Y cells. The HT-22 cells in the Co-Aβ 1–42 + OM-MSCs-Exo oe−NC group, Co-Aβ 1–42 + OM-MSCs-Exo oe−FGFR1 group, Co-Aβ 1–42 + OM-MSCs-Exo oe−FGFR1 + si-NC group, and Co-Aβ 1–42 + OM-MSCs-Exo oe−FGFR1 + si-PLCγ1 group were co-cultured with the corresponding BV2 cells for 24 h. The SH-SY5Y cells in the Co-Aβ 1–42 + OM-MSCs-Exo oe−NC group, Co-Aβ 1–42 + OM-MSCs-Exo oe−FGFR1 group, Co-Aβ 1–42 + OM-MSCs-Exo oe−FGFR1 + si-NC group, and Co-Aβ 1–42 + OM-MSCs-Exo oe−FGFR1 + si-PLCγ1 group were co-cultured with the corresponding HMC3 cells for 24 h ( n = 3). * p < 0.05, ** p < 0.01, *** p < 0.001. Normality was confirmed using the Shapiro–Wilk test. Thereafter, data were analyzed with a one-way ANOVA (followed by Tukey’s post hoc test) for multiple-group comparisons

Journal: Molecular Neurobiology

Article Title: Olfactory Mucosa Mesenchymal Stem Cell–Derived Exosomes Enhance Microglia M2 Polarization via the FGFR1/PLCγ1 Axis to Alleviate Alzheimer’s Disease

doi: 10.1007/s12035-026-05797-w

Figure Lengend Snippet: OM-MSCs-Exo delivered FGFR1 to interact with PLCγ1 in microglia, suppressing the inflammatory response of co-cultured HT-22 and SH-SY5Y cells. A CCK8 assay in HT-22 and SH-SY5Y cells. B The apoptosis rate of neurons cells was analyzed by flow cytometry. C IL-1β, TNF-α, and IL-6 levels of HT-22 and SH-SY5Y cells. The HT-22 cells in the Co-Aβ 1–42 + OM-MSCs-Exo oe−NC group, Co-Aβ 1–42 + OM-MSCs-Exo oe−FGFR1 group, Co-Aβ 1–42 + OM-MSCs-Exo oe−FGFR1 + si-NC group, and Co-Aβ 1–42 + OM-MSCs-Exo oe−FGFR1 + si-PLCγ1 group were co-cultured with the corresponding BV2 cells for 24 h. The SH-SY5Y cells in the Co-Aβ 1–42 + OM-MSCs-Exo oe−NC group, Co-Aβ 1–42 + OM-MSCs-Exo oe−FGFR1 group, Co-Aβ 1–42 + OM-MSCs-Exo oe−FGFR1 + si-NC group, and Co-Aβ 1–42 + OM-MSCs-Exo oe−FGFR1 + si-PLCγ1 group were co-cultured with the corresponding HMC3 cells for 24 h ( n = 3). * p < 0.05, ** p < 0.01, *** p < 0.001. Normality was confirmed using the Shapiro–Wilk test. Thereafter, data were analyzed with a one-way ANOVA (followed by Tukey’s post hoc test) for multiple-group comparisons

Article Snippet: According to the instruction manuals of the mouse interleukin (IL)−1β (CSB-E08054m; Cusabio), tumor necrosis factor (TNF)-α (CSB-E04741m; Cusabio), IL-6 (CSB-E04639m; Cusabio), and Aβ 1–42 (CSB-E10787m; Cusabio) detection kits, the corresponding molecular levels in cells or tissues were measured.

Techniques: Cell Culture, CCK-8 Assay, Flow Cytometry

OM-MSCs-Exo alleviated cognitive impairment and neuroinflammation in AD mice through FGFR1. A Swimming distance, swimming time, number of platform arrivals, and latency to first entry ( n = 6). B The hippocampal tissues of mice were stained with HE. C Nissl staining was performed in the hippocampus of mice. D TUNEL assay. E Data plot of the TUNEL assay. F Levels of IL-1β, TNF-α, and IL-6 in mice hippocampus. G WB analysis of Aβ, p-Tau/Tau in mice hippocampus. H Aβ 1–42 levels were detected. I FGFR1 and PLCγ1 levels were measured. J Levels of p-NF-κB/NF-κB. K , L IF staining of CD86 and CD206 in mice hippocampus. M Levels of microglia M1 and M2 polarization–related factors in mice hippocampus ( n = 5). * p < 0.05, ** p < 0.01, *** p < 0.001. Normality was confirmed using the Shapiro–Wilk test. Thereafter, data were analyzed with a one-way ANOVA (followed by Tukey’s post hoc test) for multiple-group comparisons

Journal: Molecular Neurobiology

Article Title: Olfactory Mucosa Mesenchymal Stem Cell–Derived Exosomes Enhance Microglia M2 Polarization via the FGFR1/PLCγ1 Axis to Alleviate Alzheimer’s Disease

doi: 10.1007/s12035-026-05797-w

Figure Lengend Snippet: OM-MSCs-Exo alleviated cognitive impairment and neuroinflammation in AD mice through FGFR1. A Swimming distance, swimming time, number of platform arrivals, and latency to first entry ( n = 6). B The hippocampal tissues of mice were stained with HE. C Nissl staining was performed in the hippocampus of mice. D TUNEL assay. E Data plot of the TUNEL assay. F Levels of IL-1β, TNF-α, and IL-6 in mice hippocampus. G WB analysis of Aβ, p-Tau/Tau in mice hippocampus. H Aβ 1–42 levels were detected. I FGFR1 and PLCγ1 levels were measured. J Levels of p-NF-κB/NF-κB. K , L IF staining of CD86 and CD206 in mice hippocampus. M Levels of microglia M1 and M2 polarization–related factors in mice hippocampus ( n = 5). * p < 0.05, ** p < 0.01, *** p < 0.001. Normality was confirmed using the Shapiro–Wilk test. Thereafter, data were analyzed with a one-way ANOVA (followed by Tukey’s post hoc test) for multiple-group comparisons

Article Snippet: According to the instruction manuals of the mouse interleukin (IL)−1β (CSB-E08054m; Cusabio), tumor necrosis factor (TNF)-α (CSB-E04741m; Cusabio), IL-6 (CSB-E04639m; Cusabio), and Aβ 1–42 (CSB-E10787m; Cusabio) detection kits, the corresponding molecular levels in cells or tissues were measured.

Techniques: Staining, TUNEL Assay