primary human coronary artery endothelial cells  (PromoCell)

Journal: Frontiers in Pediatrics

Article Title: MPC1 promotes the damage of human coronary endothelial cells in macrolide-resistant mycoplasma pneumoniae via inhibiting mitophagy

doi: 10.3389/fped.2026.1731155

Figure Lengend Snippet: MRMP mediates upregulation of MPC1. (A) MPC1 mRNA expression in MRMP-infected HCAECs was determined using qRT-PCR ( n = 3). (B,C) MPC1 protein expression in MRMP-infected HCAECs was determined using Western blot ( n = 3). ** p < 0.01, one-way ANOVA followed by Tukey's post hoc test.

Article Snippet: Human coronary endothelial cells (HCAECs) were purchased from ATCC, USA.

Techniques: Expressing, Infection, Quantitative RT-PCR, Western Blot

Journal: Frontiers in Pediatrics

Article Title: MPC1 promotes the damage of human coronary endothelial cells in macrolide-resistant mycoplasma pneumoniae via inhibiting mitophagy

doi: 10.3389/fped.2026.1731155

Figure Lengend Snippet: UK5099 alleviates MRMP-induced mitochondrial damage (A) mitochondrial morphology was imaged using TEM ( n = 3). Scale bar: 500 nm. (B) Quantification of the average individual mitochondrial area ( n = 3). (C,D) mRNA levels in MRMP-infected HCAECs were determined using qRT-PCR ( n = 3). (E–J) Protein expression in MRMP-infected HCAECs was determined using Western blot ( n = 3). ** p < 0.01, one-way ANOVA followed by Tukey’s post hoc test.

Article Snippet: Human coronary endothelial cells (HCAECs) were purchased from ATCC, USA.

Techniques: Infection, Quantitative RT-PCR, Expressing, Western Blot

Journal: Frontiers in Pediatrics

Article Title: MPC1 promotes the damage of human coronary endothelial cells in macrolide-resistant mycoplasma pneumoniae via inhibiting mitophagy

doi: 10.3389/fped.2026.1731155

Figure Lengend Snippet: UK5099 alleviates MRMP-induced pyroptosis of HCAECs. (A,B) Cytokine release was determined using ELISA ( n = 3). (C) Cell viability was determined using CCK-8 assay ( n = 3). (D) Cytotoxicity was determined using LDH assay. (E,F) Cell death was determined using TUNEL assay ( n = 3). Scale bar: 50 μm. (G–J) Protein expression in MRMP-infected HCAECs was determined using Western blot ( n = 3). ** p < 0.01, one-way ANOVA followed by Tukey's post hoc test.

Article Snippet: Human coronary endothelial cells (HCAECs) were purchased from ATCC, USA.

Techniques: Enzyme-linked Immunosorbent Assay, CCK-8 Assay, Lactate Dehydrogenase Assay, TUNEL Assay, Expressing, Infection, Western Blot

Journal: Frontiers in Pediatrics

Article Title: MPC1 promotes the damage of human coronary endothelial cells in macrolide-resistant mycoplasma pneumoniae via inhibiting mitophagy

doi: 10.3389/fped.2026.1731155

Figure Lengend Snippet: MG132-mediated PINK1 deficiency induces mitochondrial damage. (A) Mitochondrial morphology was imaged using TEM ( n = 3). Scale bar: 500 nm. (B) Quantification of the average individual mitochondrial area ( n = 3). (C,D) mRNA levels in MRMP-infected HCAECs were determined using qRT-PCR ( n = 3). (E,F) Protein expression in MRMP-infected HCAECs was determined using Western blot ( n = 3). ** p < 0.01, one-way ANOVA followed by Tukey's post hoc test.

Article Snippet: Human coronary endothelial cells (HCAECs) were purchased from ATCC, USA.

Techniques: Infection, Quantitative RT-PCR, Expressing, Western Blot

Journal: Frontiers in Pediatrics

Article Title: MPC1 promotes the damage of human coronary endothelial cells in macrolide-resistant mycoplasma pneumoniae via inhibiting mitophagy

doi: 10.3389/fped.2026.1731155

Figure Lengend Snippet: MG132-mediated PINK1 deficiency induces pyroptosis of HCAECs. (A,B) Cytokine release was determined using ELISA ( n = 3). (C) Cell viability was determined using CCK-8 assay ( n = 3). (D) Cytotoxicity was determined using LDH assay ( n = 3). (E,F) Cell death was determined using TUNEL assay ( n = 3). Scale bar: 50 μm. (G–J) Protein expression in MRMP-infected HCAECs was determined using Western blot ( n = 3). ** p < 0.01, one-way ANOVA followed by Tukey's post hoc test.

Article Snippet: Human coronary endothelial cells (HCAECs) were purchased from ATCC, USA.

Techniques: Enzyme-linked Immunosorbent Assay, CCK-8 Assay, Lactate Dehydrogenase Assay, TUNEL Assay, Expressing, Infection, Western Blot

Journal: Frontiers in Pediatrics

Article Title: MPC1 promotes the damage of human coronary endothelial cells in macrolide-resistant mycoplasma pneumoniae via inhibiting mitophagy

doi: 10.3389/fped.2026.1731155

Figure Lengend Snippet: MPC1 induces pyroptosis of HCAECs via inhibiting PINK1-dependent mitophagy. (A–D) Protein expression in MRMP-infected HCAECs was determined using Western blot ( n = 3). (E,F) Cytokine release was determined using ELISA ( n = 3). (G) Cell viability was determined using CCK-8 assay ( n = 3). (H) Cytotoxicity was determined using LDH assay ( n = 3). (I,J) Cell death was determined using TUNEL assay ( n = 3). Scale bar: 50 μm. (K–N) Protein expression in MRMP-infected HCAECs was determined using Western blot ( n = 3). ** p < 0.01, one-way ANOVA followed by Tukey's post hoc test.

Article Snippet: Human coronary endothelial cells (HCAECs) were purchased from ATCC, USA.

Techniques: Expressing, Infection, Western Blot, Enzyme-linked Immunosorbent Assay, CCK-8 Assay, Lactate Dehydrogenase Assay, TUNEL Assay

Journal: Frontiers in Toxicology

Article Title: Monocyte migration assay using a vascular-on-a-chip model and its utilization for the evaluation of a heated tobacco product

doi: 10.3389/ftox.2025.1658093

Figure Lengend Snippet: Barrier impairment, monocyte adhesion, and migration in VoC with or without proinflammatory cytokines and chemokines. The effect of 10 ng/mL IL-1β or 10 ng/mL TNF-α with or without MCP-1 on (A) the TEER of HCAECs after exposure for 24 h (N = 2, n = 2–4), (B) monocyte adhesion to HCAECs 2 h after the addition of monocytes (N = 2, n = 2–4), and (C) monocyte migration through HCAECs 48 h after the addition of monocytes (N = 2, n = 2–4). Data represent the mean ±95%CI, and open circles in each group represent individual chips. Statistical analysis was performed using the Kruskal–Wallis test followed by Dunn’s test for all pairs of samples for joint rank testing with Bonferroni correction. Asterisks indicate a statistically significant difference, and their colors indicate which groups were compared pairwise (* p < 0.05, ** p < 0.01). VoC, Vascular-on-a-Chip; IL, interleukin; TNF, tumor necrosis factor; MCP, monocyte chemotactic protein; TEER, trans-endothelial electrical resistance; HCAEC, human coronary artery endothelial cell; CI, confidence interval.

Article Snippet: Primary human coronary artery endothelial cells (HCAECs) were purchased from Promocell GmbH (Heidelberg, Germany) and cultured in a collagen-coated flask with Endothelial Cell Growth Medium MV2 (Promocell) containing 1% penicillin-streptomycin (FUJIFILM Wako Pure Chemical Corporation).

Techniques: Migration

Journal: Frontiers in Toxicology

Article Title: Monocyte migration assay using a vascular-on-a-chip model and its utilization for the evaluation of a heated tobacco product

doi: 10.3389/ftox.2025.1658093

Figure Lengend Snippet: Representative images of adhered monocytes and migrated monocytes in VoC treated with proinflammatory cytokines Monocyte adhesion and migration were analyzed by fluorescent imaging. After allowing fluorescently labeled monocytes to flow for 2 h (monocyte adhesion) or 48 h (monocyte migration), images of (A) monocyte adhesion and (B) monocyte migration were obtained. Scale bar = 100 μm. White dashed line indicates the boundary between the tubule structure of HCAECs and the ECM region. VoC, Vascular-on-a-Chip; HCAEC, human coronary artery endothelial cell; ECM, extracellular matrix.

Article Snippet: Primary human coronary artery endothelial cells (HCAECs) were purchased from Promocell GmbH (Heidelberg, Germany) and cultured in a collagen-coated flask with Endothelial Cell Growth Medium MV2 (Promocell) containing 1% penicillin-streptomycin (FUJIFILM Wako Pure Chemical Corporation).

Techniques: Migration, Imaging, Labeling

Journal: Frontiers in Toxicology

Article Title: Monocyte migration assay using a vascular-on-a-chip model and its utilization for the evaluation of a heated tobacco product

doi: 10.3389/ftox.2025.1658093

Figure Lengend Snippet: Effects of LPS-conditioned medium on the barrier integrity of HCAECs, and adhesion and migration of monocytes. (A) The TEER of HCAECs after 24 h of exposure to LPS-conditioned medium (N = 4, n = 5 or 6). (B) Monocyte adhesion to HCAECs 2 h after the addition of monocytes (N = 4, n = 5 or 6), and (C) monocyte migration through HCAECs 48 h after the addition of monocytes (N = 4, n = 5 or 6). Data represent the mean ±95%CI, and open circles in each group represent the value of each biological replicate. Statistical analysis was performed using the Mann–Whitney U -test. Asterisks indicate a statistically significant difference, and their colors indicate which groups were compared pairwise (*** p < 0.001). LPS, lipopolysaccharide; HCAEC, human coronary artery endothelial cell; TEER, trans-endothelial electrical resistance; DMSO, dimethyl sulfoxide; CI, confidence interval.

Article Snippet: Primary human coronary artery endothelial cells (HCAECs) were purchased from Promocell GmbH (Heidelberg, Germany) and cultured in a collagen-coated flask with Endothelial Cell Growth Medium MV2 (Promocell) containing 1% penicillin-streptomycin (FUJIFILM Wako Pure Chemical Corporation).

Techniques: Migration, MANN-WHITNEY

Journal: Frontiers in Toxicology

Article Title: Monocyte migration assay using a vascular-on-a-chip model and its utilization for the evaluation of a heated tobacco product

doi: 10.3389/ftox.2025.1658093

Figure Lengend Snippet: Effects of 1R6F TPM- and DT3.0a ACM-conditioned medium on the barrier integrity of HCAECs, and adhesion and migration of monocytes. VoC were exposed to 1R6F TPM-conditioned medium or DT3.0a ACM-conditioned medium for 24 h. (A) The TEER of HCAECs after 24 h of exposure to 1R6F TPM-conditioned medium or DT3.0a ACM-conditioned medium (N = 4, n = 5 or 6). After 24 h of exposure and the measurement of TEER, fluorescently labeled monocytes were added. (B) The number of monocytes adhered to HCAECs at 2 h (N = 4, n = 5 or 6) and (C) the number of monocytes migrated through HCAECs 48 h after the perfusion of monocytes (N = 4, n = 5 or 6). Data represent the mean ±95%CI, and open circles in each group represent the value of each biological replicate. Statistical analysis was performed using the Kruskal–Wallis test followed by Dunn’s test for all pairs of samples for joint rank testing with Bonferroni correction. Asterisks indicate a statistically significant difference, and their colors indicate which groups were compared pairwise (** p < 0.01, *** p < 0.001). TPM, total particulate matter; ACM, aerosol collected mass; DT3.0a, Direct Heating Tobacco System Platform 3 Generation 0 version a; HCAEC, human coronary artery endothelial cell; TEER, trans-endothelial electrical resistance; DMSO, dimethyl sulfoxide; CI, confidence interval.

Article Snippet: Primary human coronary artery endothelial cells (HCAECs) were purchased from Promocell GmbH (Heidelberg, Germany) and cultured in a collagen-coated flask with Endothelial Cell Growth Medium MV2 (Promocell) containing 1% penicillin-streptomycin (FUJIFILM Wako Pure Chemical Corporation).

Techniques: Migration, Labeling, Aerosol