Antifungal Efficacy of 3D-Cultured Palatal Mesenchymal Stem Cells and Their Secreted Factors against Candida albicans.

IF 3.8 2区 医学 Q2 CHEMISTRY, MEDICINAL
Mesude Bicer, Esengül Öztürk, Fatma Sener, Sema S Hakki, Özkan Fidan
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引用次数: 0

Abstract

Candida albicans is among the life-threatening fungal species and the primary contributor to hospital-acquired systemic infections, accounting for nearly 70% of all fungal infections worldwide. The current treatment primarily relies on azoles, pyrimidine analogs, polyenes, and echinocandins. However, growing antifungal resistance highlights the urgent need for the development of alternative treatments against C. albicans. Mesenchymal stem cells (MSCs) offer huge therapeutic potential for the treatment of C. albicans-associated diseases. In this study, palatal adipose tissue-derived MSCs (PAT-MSCs) and PAT-MSCs cultured in 3D biomaterial using nanofibrillar cellulose were tested against C. albicans strains ATCC 10231 and ATCC MYA 2876 using an in vitro antifungal activity assay. In addition, the conditioned medium from both PAT-MSCs and PAT-MSCs cultured in 3D hydrogel biomaterial (CM-PAT-MSCs-3D) were evaluated for their antifungal activities. The combined effect of PAT-MSCs and their secreted factors was also investigated. The expression of five antimicrobial peptide (AMP)-encoding genes was analyzed by quantitative real-time PCR. The expression of antimicrobial peptides was further confirmed via immunocytochemical staining. PAT-MSCs significantly inhibited the growth of C. albicans strains at varying inoculum concentrations (500 and 2000 CFU). Similarly, a comparable antifungal effect was observed when Candida strains were treated with PAT-MSC secreted factors alone. Statistical analysis revealed significant differences between the antifungal activities of PAT-MSCs and CM-PAT-MSCs. Lastly, the combination of PAT-MSCs and CM-PAT-MSC-3D led to a marked reduction in fungal growth, with inhibition rates of 99.75% and 99.91% for C. albicans ATCC 10231 and ATCC MYA-2876, respectively, at 500 CFU inocula. At 2000 CFU inocula, inhibition rates were 99.54% and 99.91%, respectively (****P ≤ 0.0001). These antifungal activities were further confirmed by using RT-PCR and immunocytochemical analysis. Our findings underscore a perspective on the potent antifungal activity of secreted factors from PAT-MSCs cultured within a 3D hydrogel matrix, specifically against various strains of C. albicans. Particularly, the combination of PAT-MSCs with their secreted factors represents a promising therapeutic platform, potentially offering a safer and more effective alternative to conventional antifungal treatments.

3d培养腭间充质干细胞及其分泌因子对白色念珠菌的抑菌作用。
白色念珠菌是危及生命的真菌之一,也是医院获得性全身性感染的主要原因,占全世界所有真菌感染的近70%。目前的治疗主要依赖于唑类、嘧啶类似物、多烯和棘白菌素。然而,日益增长的抗真菌耐药性突出了迫切需要开发针对白色念珠菌的替代治疗方法。间充质干细胞(MSCs)为治疗白色念珠菌相关疾病提供了巨大的治疗潜力。在这项研究中,使用纳米纤维纤维素在3D生物材料中培养的腭脂肪组织来源的间充质干细胞(PAT-MSCs)和PAT-MSCs对白色念珠菌ATCC 10231和ATCC MYA 2876进行了体外抗真菌活性测试。此外,我们还对PAT-MSCs和3D水凝胶生物材料(CM-PAT-MSCs-3D)培养的PAT-MSCs条件培养基的抗真菌活性进行了评估。研究了PAT-MSCs及其分泌因子的联合作用。采用实时荧光定量PCR技术分析5个抗菌肽(AMP)编码基因的表达情况。免疫细胞化学染色进一步证实抗菌肽的表达。在不同的接种浓度(500和2000 CFU)下,PAT-MSCs显著抑制白色念珠菌的生长。同样,当假丝酵母菌株单独用PAT-MSC分泌因子处理时,观察到类似的抗真菌效果。统计分析显示,PAT-MSCs与CM-PAT-MSCs的抗真菌活性存在显著差异。最后,PAT-MSCs与CM-PAT-MSC-3D联合使用可显著降低真菌生长,接种500 CFU时,对白色念珠菌ATCC 10231和ATCC MYA-2876的抑制率分别为99.75%和99.91%。接种2000次CFU时,抑制率分别为99.54%和99.91% (****P≤0.0001)。通过RT-PCR和免疫细胞化学分析进一步证实了这些抗真菌活性。我们的发现强调了在3D水凝胶基质中培养的PAT-MSCs分泌因子的有效抗真菌活性的观点,特别是针对各种白色念珠菌菌株。特别是,PAT-MSCs与其分泌因子的结合代表了一个有前景的治疗平台,可能提供一种比传统抗真菌治疗更安全、更有效的替代方案。
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来源期刊
ACS Infectious Diseases
ACS Infectious Diseases CHEMISTRY, MEDICINALINFECTIOUS DISEASES&nb-INFECTIOUS DISEASES
CiteScore
9.70
自引率
3.80%
发文量
213
期刊介绍: ACS Infectious Diseases will be the first journal to highlight chemistry and its role in this multidisciplinary and collaborative research area. The journal will cover a diverse array of topics including, but not limited to: * Discovery and development of new antimicrobial agents — identified through target- or phenotypic-based approaches as well as compounds that induce synergy with antimicrobials. * Characterization and validation of drug target or pathways — use of single target and genome-wide knockdown and knockouts, biochemical studies, structural biology, new technologies to facilitate characterization and prioritization of potential drug targets. * Mechanism of drug resistance — fundamental research that advances our understanding of resistance; strategies to prevent resistance. * Mechanisms of action — use of genetic, metabolomic, and activity- and affinity-based protein profiling to elucidate the mechanism of action of clinical and experimental antimicrobial agents. * Host-pathogen interactions — tools for studying host-pathogen interactions, cellular biochemistry of hosts and pathogens, and molecular interactions of pathogens with host microbiota. * Small molecule vaccine adjuvants for infectious disease. * Viral and bacterial biochemistry and molecular biology.
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