98%
921
2 minutes
20
Intestinal fibrosis is a common complication of inflammatory bowel disease but remains difficult to detect. Matrix metalloproteases (MMPs) have key roles in fibrosis and are therefore potential targets for fibrosis detection. We determined whether immunoPET of F(ab') antibody fragments targeting MMPs detects colitis induced colonic fibrosis. Mice were administered 2% dextran sulfate sodium treated water for 1 cycle (inflamed) or 3 cycles (fibrotic), or were untreated (control). Colonic and kidney collagen, innate cytokine, MMPs and fecal MPO concentrations were analyzed by multiplex/ELISA. α-pro-MMP-9 F(ab') fragments were engineered and conjugated to Zr for PET imaging, ex-vivo Cherenkov analysis and bio-distribution. Colonic innate cytokine concentrations and fecal myeloperoxidase were increased in inflamed mice but not fibrotic mice, while collagen concentrations were increased in fibrotic mice. MMPs were increased in inflamed mice, but only pro-MMP-9 remained increased in fibrotic mice. Zr-pro-MMP-9 F(ab') uptake was increased in the intestine but also in the kidney of fibrotic mice, where collagen and pro-MMP-9 concentrations were increased. Zr-pro-MMP-9 F(ab') detects colitis induced intestinal fibrosis and associated kidney fibrosis.
Download full-text PDF |
Source |
---|---|
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7683569 | PMC |
http://dx.doi.org/10.1038/s41598-020-77390-7 | DOI Listing |
Nan Fang Yi Ke Da Xue Xue Bao
August 2025
Key Laboratory of Tropical Biological Resources of Ministry of Education, School of Pharmaceutical Sciences, Hainan University, Haikou 570228, China.
Objectives: To investigate the effect of (HP) on bleomycin (BLM)-induced pulmonary fibrosis in mice and on TGF-β1-induced human fetal lung fibroblasts (HFL1).
Methods: Thirty male C57BL/6 mice were randomly divided into control group, BLM-induced pulmonary fibrosis model group, low- and high-dose HP treatment groups (3 and 21 mg/kg, respectively), and 300 mg/kg pirfenidone (positive control) group. The effects of drug treatment for 21 days were assessed by examining respiratory function, lung histopathology, and expression of fibrosis markers in the lung tissues of the mouse models.
Exp Cell Res
September 2025
Department of Nephrology, The First Hospital of China Medical University, Shenyang 110004 Liaoning Province, China. Electronic address:
Renal fibrosis is the common pathological outcome of chronic kidney disease (CKD) progressing into end-stage renal disease. The excessive proliferation of fibroblasts plays an important role in the CKD progression. Nutrients such as amino acids and their transportation are essential for cell proliferation.
View Article and Find Full Text PDFBiochem Biophys Res Commun
September 2025
Guangdong Province Hospital for Occupational Diseases Prevention and Treatment, Guangzhou, China; School of Public Health, Southern Medical University, Guangzhou, China. Electronic address:
Background: Silicosis, a devastating occupational lung disease caused by silica dust inhalation, lacks effective treatment options. Evodiamine (Evo), a bioactive alkaloid, has demonstrated anti-fibrotic potential in various diseases; however, its efficacy in silicosis and underlying mechanisms remain elusive. This study aims to systematically investigate Evo's therapeutic effects and mechanisms against silicosis.
View Article and Find Full Text PDFJ Cell Mol Med
September 2025
Department of Radiation Oncology, The First Affiliated Hospital of Nanjing Medical University, Nanjing, China.
Cardiac fibrosis, especially in the infarct border zone, leads to decreased cardiac compliance, impaired systolic and diastolic function, resulting in heart failure. M6A methylation plays a role in fibrosis development. However, its underlying mechanism remains poorly understood.
View Article and Find Full Text PDFNat Mater
September 2025
Department of Materials Science and Engineering, University of Michigan, Ann Arbor, MI, USA.
Within most tissues, the extracellular microenvironment provides mechanical cues that guide cell fate and function. Changes in the extracellular matrix such as aberrant deposition, densification and increased crosslinking are hallmarks of late-stage fibrotic diseases that often lead to organ dysfunction. Biomaterials have been widely used to mimic the mechanical properties of the fibrotic matrix and study pathophysiologic cell function.
View Article and Find Full Text PDF