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TG2 suppression modulated proteins associated with ECM maintenance, inflammation, apoptosis, and TGF-β signaling in rTGF-β-treated hPTECs and <t>NIH3T3</t> cells. (A) Western blots of fibronectin, periostin, collagen type IV, TNF-α, integrin-α5, and β-actin of hPTECs treated with rTGF-β and cysteamine (48 h), and (B) densitometric quantification normalized to β-actin. (C) Western blots of fibronectin, periostin, collagen type I-α1, integrin-α5, and β-actin of NIH3T3 cells treated with rTGF-β and cysteamine (24 h), and (D) densitometric quantification normalized to β-actin. (E) Light microscopic images of hPTECs and (F) NIH3T3 cells treated with rTGF-β and cysteamine. (G) Annexin V and propidium iodide (PI) staining of human proximal tubular epithelial cells (hPTECs) treated with rTGF-β and cysteamine (48 h), and (H) quantification. Statistical significance: * P ≤ 0.05, ** P ≤ 0.01, *** P ≤ 0.001.
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TG2 suppression modulated proteins associated with ECM maintenance, inflammation, apoptosis, and TGF-β signaling in rTGF-β-treated hPTECs and NIH3T3 cells. (A) Western blots of fibronectin, periostin, collagen type IV, TNF-α, integrin-α5, and β-actin of hPTECs treated with rTGF-β and cysteamine (48 h), and (B) densitometric quantification normalized to β-actin. (C) Western blots of fibronectin, periostin, collagen type I-α1, integrin-α5, and β-actin of NIH3T3 cells treated with rTGF-β and cysteamine (24 h), and (D) densitometric quantification normalized to β-actin. (E) Light microscopic images of hPTECs and (F) NIH3T3 cells treated with rTGF-β and cysteamine. (G) Annexin V and propidium iodide (PI) staining of human proximal tubular epithelial cells (hPTECs) treated with rTGF-β and cysteamine (48 h), and (H) quantification. Statistical significance: * P ≤ 0.05, ** P ≤ 0.01, *** P ≤ 0.001.

Journal: Frontiers in Physiology

Article Title: A comprehensive approach to elucidating the pathophysiology of kidney fibrosis based on extracellular vesicle proteomics

doi: 10.3389/fphys.2026.1786999

Figure Lengend Snippet: TG2 suppression modulated proteins associated with ECM maintenance, inflammation, apoptosis, and TGF-β signaling in rTGF-β-treated hPTECs and NIH3T3 cells. (A) Western blots of fibronectin, periostin, collagen type IV, TNF-α, integrin-α5, and β-actin of hPTECs treated with rTGF-β and cysteamine (48 h), and (B) densitometric quantification normalized to β-actin. (C) Western blots of fibronectin, periostin, collagen type I-α1, integrin-α5, and β-actin of NIH3T3 cells treated with rTGF-β and cysteamine (24 h), and (D) densitometric quantification normalized to β-actin. (E) Light microscopic images of hPTECs and (F) NIH3T3 cells treated with rTGF-β and cysteamine. (G) Annexin V and propidium iodide (PI) staining of human proximal tubular epithelial cells (hPTECs) treated with rTGF-β and cysteamine (48 h), and (H) quantification. Statistical significance: * P ≤ 0.05, ** P ≤ 0.01, *** P ≤ 0.001.

Article Snippet: The cells were incubated at 37 °C and 5% CO 2 for 48 h. NIH3T3 cells (ATCC: CRL-1658) were maintained in DMEM/F12 (Biowest, Riverside, MO, USA; Cat# L0092) supplemented with 10% FBS (Gibco, Cat# A4766801) and 1% 100X penicillin-streptomycin (Gibco, Cat# 15140-122).

Techniques: Western Blot, Staining