Nanotechnology in Gene Editing: Pioneering CRISPR‐Cas Delivery Systems to Tackle Antibiotic Resistance DOI Open Access
Sahar Gholamian,

Pooya Baghaee,

Mohammad Doroudian

и другие.

Advanced Therapeutics, Год журнала: 2025, Номер unknown

Опубликована: Март 3, 2025

Abstract The rise of antibiotic‐resistant bacteria, driven by antibiotic misuse, is a major global health threat. Addressing this issue requires understanding resistance mechanisms and developing innovative solutions. Clustered Regularly Interspaced Short Palindromic Repeats (CRISPR)‐associated systems (Cas), genome‐editing tool derived from prokaryotic defense mechanisms, offers precise targeting genes. By reprogramming CRISPR‐Cas, bacteria can be killed or resensitized to antibiotics through plasmid curing. However, clinical applications face challenges, particularly in delivering CRISPR‐Cas components effectively. Nanotechnology has emerged as promising approach for targeted delivery tissues cells. This paper explores the molecular resistance, emphasizing structure function their mechanisms. It highlights use nanoparticles (NPs) nanoscale carriers deliver components, reviewing recent studies that combine NPs CRISPR target Additionally, discusses current challenges future prospects field, underscoring potential nanotechnology combat resistance.

Язык: Английский

Mesenchymal Stem Cell-Derived Small Extracellular Vesicles: A Novel Approach for Kidney Disease Treatment DOI Creative Commons
Yukang Lu, Lanfeng Wang, Mengting Zhang

и другие.

International Journal of Nanomedicine, Год журнала: 2022, Номер Volume 17, С. 3603 - 3618

Опубликована: Авг. 1, 2022

Abstract: Globally, kidney disease has become a serious health challenge, with approximately 10% of adults suffering the disease, and increasing incidence mortality rates every year. Small extracellular vesicles (sEVs) are 30 nm– 100 nm sized nanovesicles released by cells into matrix (ECM), which serve as mediators intercellular communication. Depending on cell origin, sEVs have different roles depend internal cargoes including, nucleic acids, proteins, lipids. Mesenchymal stem (MSCs) exert anti-inflammatory, anti-aging, wound healing functions mainly via in stable safe manner. MSC-derived (MSC-sEVs) several diseases transporting renoprotective to reduce oxidative stress, inhibit renal apoptosis, suppress inflammation, mediate anti-fibrosis mechanisms. Additionally, because MSC-sEVs efficiently target damaged kidneys, they potential next generation cell-free therapies for disease. Herein, we review recent research data how could be used treat Keywords: small vesicles, mesenchymal cells, acute injury, chronic carcinoma

Язык: Английский

Процитировано

24

COVID-19 inflammation and implications in drug delivery DOI
Makhloufi Zoulikha, Feifei Huang, Zhenfeng Wu

и другие.

Journal of Controlled Release, Год журнала: 2022, Номер 346, С. 260 - 274

Опубликована: Апрель 27, 2022

Язык: Английский

Процитировано

23

Mesenchymal Stem Cell-Derived Antimicrobial Peptides as Potential Anti-Neoplastic Agents: New Insight into Anticancer Mechanisms of Stem Cells and Exosomes DOI Creative Commons
Kasra Moeinabadi‐Bidgoli, Malihe Rezaee, Hamidreza Rismanchi

и другие.

Frontiers in Cell and Developmental Biology, Год журнала: 2022, Номер 10

Опубликована: Июль 6, 2022

Mesenchymal stem cells (MSCs), as adult multipotent cells, possess considerable regenerative and anti-neoplastic effects, from inducing apoptosis in the cancer to reducing multidrug resistance that bring them up an appropriate alternative for treatment. These can alter behavior of condition tumor microenvironment, activity immune result regression. It has been observed during inflammatory conditions, a well-known feature MSCs produce release some molecules called "antimicrobial peptides (AMPs)" with demonstrated effects. have remarkable targeted anticancer effects by attaching negatively charged membrane neoplastic disrupting membrane, interfering intracellular pathways. Therefore, AMPs could be considered part wide-ranging MSCs. This review focuses on possible MSCs-derived their mechanisms. also discusses preconditioning approaches using exosomes enhance AMP production delivery cells. Besides, clinical administration AMPs, along challenges practice, were debated.

Язык: Английский

Процитировано

21

Mesenchymal stem cells and their derived exosomes for ALI/ARDS: A promising therapy DOI Creative Commons
Dan Liang, Chang Liu, Mei Yang

и другие.

Heliyon, Год журнала: 2023, Номер 9(10), С. e20387 - e20387

Опубликована: Сен. 30, 2023

Acute lung injury (ALI)/acute respiratory distress syndrome (ARDS) is a serious clinical with high morbidity and mortality. Presently, therapeutic approaches for ALI/ARDS primarily revolve around symptomatic supportive care encompassing mechanical ventilation fluid management. Regrettably, the prognosis most patients remains bleak due to absence of effective treatment strategies. Even survivors may have long-term pulmonary dysfunction cognitive impairment. The quality life has been seriously compromised. emergence mesenchymal stem cells (MSCs) their exosomes opened up an expansive realm potential optimism addressing plight patients, as MSCs derived exhibit multifaceted capabilities, including anti-inflammatory properties, facilitation tissue repair regeneration, apoptosis inhibition. Therefore, future research should focus on possible mechanisms open new avenues applications.

Язык: Английский

Процитировано

11

Nanotechnology in Gene Editing: Pioneering CRISPR‐Cas Delivery Systems to Tackle Antibiotic Resistance DOI Open Access
Sahar Gholamian,

Pooya Baghaee,

Mohammad Doroudian

и другие.

Advanced Therapeutics, Год журнала: 2025, Номер unknown

Опубликована: Март 3, 2025

Abstract The rise of antibiotic‐resistant bacteria, driven by antibiotic misuse, is a major global health threat. Addressing this issue requires understanding resistance mechanisms and developing innovative solutions. Clustered Regularly Interspaced Short Palindromic Repeats (CRISPR)‐associated systems (Cas), genome‐editing tool derived from prokaryotic defense mechanisms, offers precise targeting genes. By reprogramming CRISPR‐Cas, bacteria can be killed or resensitized to antibiotics through plasmid curing. However, clinical applications face challenges, particularly in delivering CRISPR‐Cas components effectively. Nanotechnology has emerged as promising approach for targeted delivery tissues cells. This paper explores the molecular resistance, emphasizing structure function their mechanisms. It highlights use nanoparticles (NPs) nanoscale carriers deliver components, reviewing recent studies that combine NPs CRISPR target Additionally, discusses current challenges future prospects field, underscoring potential nanotechnology combat resistance.

Язык: Английский

Процитировано

0