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Background: Every year, millions of infants are born prematurly, many of whom develop serious complications like bronchopulmonary dysplasia and necrotizing enterocolitis. Despite improvements in neonatal care, there are few therapies that actively promote healing or prevent long-term damage. In recent years, secretions from mesenchymal stem cells, rich in reparative proteins and tiny extracellular particles have shown promise as a safe and effective way to support tissue repair without the risks of live-cell therapy.
Methods: This review brings together findings from animal studies and early-stage clinical trials to explore how these stem cell-derived secretions work and how they might be used in the clinic. We examine how different sources of mesenchymal stem cells, such as bone marrow or umbilical cord affect the quality and function of their secretions. We also look at key biological pathways they influence, including inflammation control, blood vessel growth, and tissue regeneration. In parallel, we assess the designs and outcomes of current clinical trials involving preterm infants.
Results: In animal models, these secretions have repeatedly shown the ability to reduce lung and gut injury, calm inflammation, and boost repair mechanisms. Products from umbilical cord tissue appear especially potent, delivering high levels of protective molecules while being low in immunogenic risk. Several small clinical studies report that the approach is safe and well-tolerated in preterm infants, with some signs of benefit. However, clinical use is still limited by variability in production methods and the lack of standardized dosing.
Conclusions: Mesenchymal stem cell secretions could offer a powerful new way to treat fragile preterm infants, providing regenerative support without the risks of cell transplantation. But before they become part of routine care, we need clearer guidance on how to manufacture, measure, and safely deliver these therapies in newborns.
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http://dx.doi.org/10.1186/s13287-025-04616-8 | DOI Listing |
Clin Oral Investig
September 2025
Department of Stomatology, Shengli Oilfield Central Hospital, No. 31, Jinan Road, Dongying, 257034, China.
Objective: Progesterone (PG) and its target, progesterone receptor (PGR), are important regulators in inflammatory diseases. This study aimed to investigate the specific role of PG in periodontitis and to elucidate the underlying mechanisms involving PGR.
Methods: Women with periodontitis, including 250 with PG deficiency, 250 with PG supplementation, and 245 controls (normal PG) were enrolled.
Nature
September 2025
Institute of Biomechanics and Medical Engineering, Applied Mechanics Laboratory, Department of Engineering Mechanics, Tsinghua University, Beijing, China.
The human stomach features distinct, regionalized functionalities along the anterior-posterior axis. Historically, studies on stomach patterning have used animal models to identify the underlying principles. Recently, human pluripotent stem (hPS)-cell-based gastric organoids for modelling domain-specific development of the fundic and antral epithelium are emerging.
View Article and Find Full Text PDFUltrasound Med Biol
September 2025
State Key Laboratory of Ultrasound in Medicine and Engineering, Chongqing Medical University, Chongqing, China; Chongqing Key Laboratory of Biomedical Engineering, Chongqing Medical University, Chongqing, China. Electronic address:
Objective: Diabetic foot ulcer (DFU) is a common and serious complication of diabetes, often leading to infection, amputation and poor quality of life. Bone marrow mesenchymal stem cells (BMSCs) have shown promise in treating chronic wounds, but their therapeutic efficacy is limited due to poor survival and low regenerative activity. Low-intensity pulsed ultrasound (LIUS), a non-invasive physical modality, has been shown to enhance the biological behavior of BMSCs.
View Article and Find Full Text PDFDev Cell
September 2025
Francis Crick Institute, 1 Midland Road, London NW1 1AT, UK. Electronic address:
Lineage specification requires accurate interpretation of multiple signaling cues. However, how combinatorial signaling histories influence fate outcomes remains unclear. We combined single-cell transcriptomics, live-cell imaging, and mathematical modeling to explore how activin and bone morphogenetic protein 4 (BMP4) guide fate specification during human gastrulation.
View Article and Find Full Text PDFPhytomedicine
August 2025
Zhejiang Provincial Chinese Medicine Hospital (First affiliated hospital of Zhejiang Chinese Medical University), Zhejiang Chinese Medical University, Hangzhou City, Zhejiang Province, 310053, China; Department of Orthopedics, Affiliated Hospital of Jiangxi University of Chinese Medicine, Jiangxi Un
Background: Osteoporotic osteoarthritis (OPOA), a distinct subtype of osteoarthritis (OA), has imposed a significant health and economic burden worldwide. However, mechanistic studies and therapeutic strategies for this disease remain in the exploratory stage.
Purpose: This study aimed to investigate the specific molecular mechanisms by which osteoporosis (OP) exacerbates OA progression through accelerated subchondral bone (SB) sclerosis and the potential of Jiawei Yanghe Decoction (JWYHD) in treating OPOA.