Tubular epithelial cells-derived small extracellular vesicle-VEGF-A promotes peritubular capillary repair in ischemic kidney injury DOI Creative Commons
Xin Zhong, Tao‐Tao Tang,

Anran Shen

и другие.

npj Regenerative Medicine, Год журнала: 2022, Номер 7(1)

Опубликована: Дек. 17, 2022

Peritubular capillaries (PTCs) are closely related to renal tubules in structure and function, both pivotal regulators the development progression of acute kidney injury (AKI). However, mechanisms that underlie interaction between PTCs during AKI remain unclear. Here we explored a new mode tubulovascular crosstalk mediated by small extracellular vesicles (sEV) after AKI. In response ischemia/reperfusion (I/R) injury, endothelial proliferation tubular expression vascular growth factor-A (VEGF-A) were increased, accompanied remarkable redistribution cytoplasmic VEGF-A basolateral side cells. Meanwhile, secretion was converted injured cells, which showed much greater tendency secrete via sEV other than free form. Interestingly, cell-derived VEGF-A-enriched (sEV-VEGF-A) turned out promote regulated VEGF receptors 1 2. Furthermore, inhibition Rab27a knockdown resulted significant decrease peritubular cells vivo. Importantly, taking advantage newly recognized endogenous repair PTCs, exogenous supplementation + efficiently recused PTC rarefaction, improved perfusion, halted CKD transition. Taken together, our study uncovered novel intrinsic through tubule-PTC sEV-VEGF-A, could be exploited as promising therapeutic angiogenesis strategy diseases with ischemia.

Язык: Английский

Extracellular vesicles in kidney disease DOI Open Access
Cristina Grange, Benedetta Bussolati

Nature Reviews Nephrology, Год журнала: 2022, Номер 18(8), С. 499 - 513

Опубликована: Май 31, 2022

Язык: Английский

Процитировано

123

Sensing Dying Cells in Health and Disease DOI Creative Commons

Elena Tutunea-Fatan,

Shabitha Arumugarajah,

Rita S. Suri

и другие.

Journal of the American Society of Nephrology, Год журнала: 2024, Номер 35(6), С. 795 - 808

Опубликована: Фев. 14, 2024

Kidney injury molecule-1 (KIM-1), also known as T-cell Ig and mucin domain-1 (TIM-1), is a widely recognized biomarker for AKI, but its biological function less appreciated. KIM-1/TIM-1 belongs to the domain family of conserved transmembrane proteins, which bear characteristic six-cysteine Ig-like variable domain. The latter enables binding natural ligand, phosphatidylserine, expressed on surface apoptotic cells necrotic cells. in variety tissues plays fundamental roles regulating sterile inflammation adaptive immune responses. In kidney, KIM-1 upregulated injured renal proximal tubule cells, transforms them into phagocytes clearance dying helps dampen inflammation. TIM-1, T B killer essential cell activation regulatory functions host. Functional polymorphisms gene KIM-1/TIM-1, HAVCR1 , have been associated with susceptibility immunoinflammatory conditions hepatitis A virus-induced liver failure, thought be due differential ability variants bind phosphatidylserine. This review will summarize role health disease potential clinical applications therapeutic target humans.

Язык: Английский

Процитировано

14

Nanomaterials for Targeted Therapy of Kidney Diseases: Strategies and Advances DOI Creative Commons
Zhiwen Wang, Chun Zhang

Materials Today Bio, Год журнала: 2025, Номер 31, С. 101534 - 101534

Опубликована: Янв. 29, 2025

The treatment and management of kidney diseases pose a significant global burden. Due to the presence blood circulation barriers glomerular filtration barriers, drug therapy for faces challenges such as poor renal targeting, short half-life, severe systemic side effects, severely hindering therapeutic progress. Therefore, research development kidney-targeted agents is great clinical significance. In recent years, application nanotechnology in field nephrology has shown potential revolutionizing diagnosis diseases. Carefully designed nanomaterials can exhibit optimal biological characteristics, influencing various aspects circulation, retention, excretion. Rationally designing modifying based on anatomical structure pathophysiological environment achieve highly specific or nanodrug delivery systems both feasible promising. Based targeted diseases, this review discusses advantages limitations current nanomedicine summarizes active/passive targeting strategies, order further promote through preliminary summary previous studies future prospects.

Язык: Английский

Процитировано

2

High-density lipoprotein nanoparticles spontaneously target to damaged renal tubules and alleviate renal fibrosis by remodeling the fibrotic niches DOI Creative Commons
Shanshan He, Xiaoyang Li, Yuanyuan He

и другие.

Nature Communications, Год журнала: 2025, Номер 16(1)

Опубликована: Янв. 27, 2025

Chronic kidney disease (CKD) ultimately causes renal fibrosis and end-stage disease, thus seriously threatens human health. However, current medications for CKD are inefficient, which is often due to poor targeting capability tubule. In this study, we discover that biomimetic high-density lipoprotein (bHDL) lipid nanoparticles possess excellent ability injured tubular epithelial cells by injury molecule-1(KIM-1) mediated internalization. Thus, co-load anti-inflammatory drug triptolide (TP) anti-fibrotic nintedanib (BIBF) on bHDL treat CKD. Based the targeted delivery mutual enhancement of efficacy co-delivered drugs, bHDL-based system effectively reduces alleviates in different mouse models. The mechanistic study shows BIBF TP synergistically remodel fibrotic niches decreasing inflammatory cytokines, limiting immune cell infiltration inhibiting activation myofibroblasts. vehicle also possesses high manufacturability, good safety adequately toxicity TP. promising treatment has potential delivering agents damaged cells. Effectively tubule delay or halt chronic progression remains a significant unmet clinical challenge. Here, authors introduce an innovative strategy using nanoparticles.

Язык: Английский

Процитировано

1

The efficacy of novel biomarkers for the early detection and management of acute kidney injury: A systematic review DOI Creative Commons
Mohammed Almulhim

PLoS ONE, Год журнала: 2025, Номер 20(1), С. e0311755 - e0311755

Опубликована: Янв. 29, 2025

Acute kidney injury (AKI) is a frequent clinical complication lacking early diagnostic tests and effective treatments. Novel biomarkers have shown promise for enabling earlier detection, risk stratification, guiding management of AKI. We conducted systematic review to synthesize evidence on the efficacy novel AKI detection management. Database searches yielded 17 relevant studies which were critically appraised. Key themes biomarker in predicting severity before functional changes; potential improve through diagnosis, prognostic enrichment, interventions; emerging roles as therapeutic targets tools; ongoing challenges requiring further validation. Overall, like neutrophil gelatinase-associated lipocalin (NGAL), molecule-1 (KIM-1), cell cycle arrest markers ([TIMP-2] •[IGFBP7]) demonstrate capability very prediction accurate stratification. Their incorporation has facilitate timely targeted interventions personalized However, factors influencing performance, optimal cutoffs, cost-effectiveness, impact patient outcomes require robust validation across diverse settings widespread implementation. Addressing these limitations research can help translate into improved prognosis, practice.

Язык: Английский

Процитировано

1

Engineered Macrophage Membrane-Coated Nanoparticles Attenuate Calcium Oxalate Nephrocalcinosis-Induced Kidney Injury by Reducing Oxidative Stress and Pyroptosis DOI

Xiaozhuo Ba,

Tao Ye,

Yu He

и другие.

Acta Biomaterialia, Год журнала: 2025, Номер unknown

Опубликована: Фев. 1, 2025

Язык: Английский

Процитировано

1

Emerging Frontiers in acute kidney injury: The role of extracellular vesicles DOI
Sirui Li, Lan Zhou, Yu Huang

и другие.

Bioactive Materials, Год журнала: 2025, Номер 48, С. 149 - 170

Опубликована: Фев. 18, 2025

Язык: Английский

Процитировано

1

Mesenchymal cell-derived exosomes and miR-29a-3p mitigate renal fibrosis and vascular rarefaction after renal ischemia reperfusion injury DOI Creative Commons
Jing Huang, Lang Shi, Yifei Yang

и другие.

Stem Cell Research & Therapy, Год журнала: 2025, Номер 16(1)

Опубликована: Март 12, 2025

Renal fibrosis and vascular rarefaction are significant complications of ischemia/reperfusion (I/R) injury. Human umbilical cord mesenchymal cell-derived exosomes (hucMSC-exos) have shown potential in mitigating these conditions. This study investigates the role miR-29a-3p its therapeutic effects on I/R-induced renal damage. Male C57BL/6 mice were subjected to unilateral ischemia for 28 min followed by reperfusion. Exosomes mimics/inhibitors injected into mice. function, histological analysis, molecular assays performed evaluate integrity. Exosome treatment significantly improved function reduced post-I/R. MiR-29a-3p was highly expressed hucMSC-exos but models. mimic reduced, while inhibitor exacerbated rarefaction. Collagen I TNFR1 identified as direct targets fibroblasts endothelial cells, respectively. overexpressing provided superior protection compared unmodified hucMSC-exos. HucMSC-exos, particularly those miR-29a-3p, potent against collagen I, highlighting therapy.

Язык: Английский

Процитировано

1

Lipid-Based Nanovesicular Drug Delivery Systems DOI Creative Commons
Tania Limongi, Francesca Susa, Monica Marini

и другие.

Nanomaterials, Год журнала: 2021, Номер 11(12), С. 3391 - 3391

Опубликована: Дек. 14, 2021

In designing a new drug, considering the preferred route of administration, various requirements must be fulfilled. Active molecules pharmacokinetics should reliable with valuable drug profile as well well-tolerated. Over past 20 years, nanotechnologies have provided alternative and complementary solutions to those an exclusively pharmaceutical chemical nature since scientists clinicians invested in optimization materials methods capable regulating effective delivery at nanometer scale. Among many carriers, lipid nano vesicular ones successfully support clinical candidates approaching such problems insolubility, biodegradation, difficulty overcoming skin biological barriers blood-brain one. this review, authors discussed structure, biochemical composition, applications nanovesicular namely, niosomes, proniosomes, ethosomes, transferosomes, pharmacosomes, ufasomes, phytosomes, catanionic vesicles, extracellular vesicles.

Язык: Английский

Процитировано

46

Extracellular vesicles for renal therapeutics: State of the art and future perspective DOI
Tao‐Tao Tang, Bin Wang, Lin‐Li Lv

и другие.

Journal of Controlled Release, Год журнала: 2022, Номер 349, С. 32 - 50

Опубликована: Июль 4, 2022

Язык: Английский

Процитировано

34