CRAMP诱导自噬提高烟曲霉角膜炎中巨噬细胞的杀真菌能力
CRAMP Inducing Autophagy to Improve the Fungicidal Ability of Macrophages during Aspergillus fumigatus Keratitis
DOI: 10.12677/ACM.2023.133622, PDF,   
作者: 侯晓晨, 彭旭东, 林 静*:青岛大学附属医院眼科,山东 青岛
关键词: CRAMP烟曲霉菌巨噬细胞自噬杀真菌力CRAMP Aspergillus fumigatus Macrophages Autophagy Fungicidal Ability
摘要: CRAMP是一种能够抑制多种真菌生长的抗微生物肽,据报道CRAMP在细菌感染中能够调控巨噬细胞。本文对小鼠烟曲霉菌性角膜炎中CRAMP的治疗效果及对巨噬细胞的调控展开研究。方法:体内实验通过建立小鼠烟曲霉菌角膜炎模型,比较CRAMP或PBS处理组在裂隙灯照片、临床评分以及真菌负荷方面的差异。体外实验通过流式细胞技术分析CRAMP对巨噬细胞吞噬、杀灭细胞内杀真菌力的影响。RT-PCR和免疫蛋白印迹法检测巨噬细胞自噬相关基因和蛋白的表达,如LAMP-3、Beclin-1。结果:在烟曲霉角膜炎期间,CRAMP减少了小鼠角膜的真菌负荷并降低了角膜的临床评分。虽然CRAMP对烟曲霉感染巨噬细胞的吞噬作用无显著影响,但可显著加速巨噬细胞对细胞内真菌的清除。进一步的机制研究表明,CRAMP可上调LAMP-3和Beclin-1的表达,并通过诱导自噬提高巨噬细胞胞内杀真菌能力。结论:CRAMP可诱导自噬提高巨噬细胞的杀真菌能力,改善小鼠烟曲霉角膜炎预后。
Abstract: CRAMP is an antimicrobial peptide that inhibits the growth of a variety of fungi and has been re-ported to modulate macrophages in bacterial infections. In this paper, the therapeutic effect of CRAMP on Aspergillus fumigatus keratitis in mice and the regulation of macrophage were studied. Methods: In vivo, mice models with Aspergillus fumigatus keratitis were established to compare the statistic differences in slit-lamp photographs, clinical scores, and fungal loads between the CRAMP-treated or PBS-treated groups. In vitro, the effects of CRAMP on the phagocytosis and intra-cellular fungicidal ability of macrophages were analyzed by flow cytometry. RT-PCR and Western blot were used to detect the expression of autophagy related genes and proteins of macrophages, such as LAMP-3 and Beclin-1. Results: During Aspergillus fumigatus keratitis, CRAMP reduced fun-gal loads of mice corneas and lowered clinical scores. Although CRAMP had no significant effect on the phagocytosis of macrophages infected with Aspergillus fumigatus, it could significantly acceler-ate the intracellular fungal clearance by macrophages. Further mechanism studies showed that CRAMP could up-regulate the expression of LAMP-3 and Beclin-1, and elevate the intracellular fun-gicidal ability of macrophages by inducing autophagy. Conclusion: CRAMP can induce autophagy to elevate the fungicidal ability of macrophages and improve the prognosis of Aspergillus fumigatus keratitis in mice.
文章引用:侯晓晨, 彭旭东, 林静. CRAMP诱导自噬提高烟曲霉角膜炎中巨噬细胞的杀真菌能力[J]. 临床医学进展, 2023, 13(3): 4335-4343. https://doi.org/10.12677/ACM.2023.133622

参考文献

[1] Li, C., Zhao, G., Che, C., et al. (2015) The Role of LOX-1 in Innate Immunity to Aspergillus fumigatus in Corneal Epi-thelial Cells. Investigative Ophthalmology & Visual Science, 56, 3593-3603. [Google Scholar] [CrossRef] [PubMed]
[2] Li, C., Zhao, G.Q., Che, C.Y., Lin, J., Li, N., Jia, W.Y., et al. (2012) Effect of Corneal Graft Diameter on Therapeutic Penetrating Keratoplasty for Fungal Keratitis. International Journal of Ophthalmology, 5, 698-703.
[3] He, K., Yue, L.H., Zhao, G.Q., Li, C., Lin, J., Jiang, N., et al. (2016) The Role of LOX-1 on Innate Immunity against Aspergillus fumigatus Keratitis in Mice. International Journal of Ophthalmology, 9, 1245-1250.
[4] Zhang, J., Zhao, G., Lin, J., Che, C., Li, C., Jiang, N., et al. (2016) Role of PTX3 in Corneal Epithelial Innate Immunity against Aspergillus fumigatus Infection. Experimental Eye Research, 167, 152-162. [Google Scholar] [CrossRef] [PubMed]
[5] Latgé, J.P. (1999) Aspergillusfumigatus and Aspergillosis. Clinical Microbiology Review, 12, 310-350. [Google Scholar] [CrossRef
[6] O’Day, D.M., Head, W.S., Robinson, R.D. and Clanton, J.A. (1986) Corneal Penetration of Topical Amphotericin Band Natamycin. Current Eye Research, 5, 877-882. [Google Scholar] [CrossRef] [PubMed]
[7] Peng, X.D., Zhao, G.Q., Lin, J., Jiang, N., Xu, Q., Zhu, C.C., et al. (2015) Fungus Induces the Release of IL-8 in Human Corneal Epithelial Cells, via Dectin-1-Mediated Protein Kinase C Pathways. International Journal of Ophthalmology, 8, 441-447.
[8] Kawakami, H., Inuzuka, H., Hori, N., Takahashi, N., Ishida, K., Mochizuki, K., et al. (2015) Inhibitory Effects of Antimicrobial Agents against Fusarium Species. Medical Mycology, 53, 603-611. [Google Scholar] [CrossRef] [PubMed]
[9] Yilmaz, S., Ozturk, I. and Maden, A. (2007) Microbial Keratitis in West Anatolia, Turkey: A Retrospective Review. International Ophthalmology, 27, 261-268. [Google Scholar] [CrossRef] [PubMed]
[10] Khani, S., Seyedjavadi, S.S., Hosseini, H.M., Goudarzi, M., Valadbeigi, S., Khatami, S., et al. (2020) Effects of the Antifungal Peptide Skh-AMP1 Derived from Satureja khuzistan-ica on Cell Membrane Permeability, ROS Production, and Cell Morphology of Conidia and Hyphae of Aspergillus fu-migatus. Peptides, 123, Article ID: 170195. [Google Scholar] [CrossRef] [PubMed]
[11] Amulic, B., Cazalet, C., Hayes, G.L., Metzler, K.D. and Zych-linsky, A. (2012) Neutrophil Function: From Mechanisms to Disease. Annual Review of Immunology, 30, 459-489. [Google Scholar] [CrossRef] [PubMed]
[12] Lübow, C., Bockstiegel, J. and Weindl, G. (2020) Lysosomotropic Drugs Enhance Pro-Inflammatory Responses to IL-1β in Macrophages by Inhibiting Internalization of the IL-1 Receptor. Biochemical Pharmacology, 175, Article ID 113864. [Google Scholar] [CrossRef] [PubMed]
[13] Swidergall, M., Solis, N.V., Wang, Z.P., et al. (2019) EphA2 Is a Neutrophil Receptor for Candida albicans that Stimulates Antifungal Activity during Oropharyngeal Infection. Cell Re-ports, 28, 423-433. [Google Scholar] [CrossRef] [PubMed]
[14] Yang, H., Wang, Q., Han, L., Yang, X., Zhao, W., Lyu, L., et al. (2020) Nerolidol Inhibits the LOX-1/IL-1β Signaling to Protect against the Aspergillus fumigatus Keratitis Inflammation Damage to the Cornea. International Immunopharmacology, 80, Article ID: 106118. [Google Scholar] [CrossRef] [PubMed]
[15] Meresman, G.F., Götte, M. and Laschke, M.W. (2021) Plants as Source of New Therapies for Endometriosis: A Review of Preclinical and Clinical Studies. Human Reproduction Update, 27, 367-392. [Google Scholar] [CrossRef] [PubMed]
[16] Cao, Y., Dai, B., Wang, Y., Huang, S., Xu, Y., Cao, Y., et al. (2008) In Vitro Activity of Baicalein against Candida albicans Biofilms. International Journal of Antimicrobial Agents, 32, 73-77. [Google Scholar] [CrossRef] [PubMed]
[17] Jiang, N., Zhang, L., Zhao, G., et al. (2020) Indoleamine 2,3-Dioxygenase Regulates Macrophage Recruitment, Polarization and Phagocytosis in Aspergillus fumigatus Keratitis. Investigative Ophthalmology & Visual Science, 61, 28. [Google Scholar] [CrossRef] [PubMed]
[18] Lee, H.H., Del Pozzo, J., Salamanca, S.A., et al. (2019) Reduced Phago-cytosis and Killing of Cryptococcus neoformans Biofilm-Derived Cells by J774.16 Macrophages Is Associated with Fungal Capsular Production and Surface Modification. Fungal Genetics and Biology, 132, Article ID: 103258. [Google Scholar] [CrossRef] [PubMed]
[19] Luo, X.-L., Li, J.-X., Huang, H.-R., et al. (2019) LL37 Inhibits Aspergillus fumigatus Infection via Directly Binding to the Fungus and Preventing Excessive Inflammation. Frontiers in Immunology, 10, 283. [Google Scholar] [CrossRef] [PubMed]
[20] De Ullivarri, M.F., Arbulu, S., Garcia-Gutierrez, E. and Cotter, P.D. (2020) Antifungal Peptides as Therapeutic Agents. Frontiers in Cellular and Infection Microbiology, 10, 105. [Google Scholar] [CrossRef] [PubMed]
[21] De Brucker, K., Delattin, N., Robijns, S., et al. (2014) Derivatives of the Mouse Cathelicidin-Related Antimicrobial Peptide (CRAMP) Inhibit Fungal and Bacterial Biofilm Formation. An-timicrobial Agents and Chemotherapy, 8, 5395-5404. [Google Scholar] [CrossRef
[22] Kolar, S.S., Baidouri, H. and McDermott, A.M. (2017) Role of Pattern Recognition Receptors in the Modulation of Antimicrobial Peptide Expression in the Corneal Epithelial Innate Response to F. solani. Investigative Ophthalmology & Visual Science, 58, 2463-2472. [Google Scholar] [CrossRef] [PubMed]
[23] Lim, R., Barker, G. and Lappas, M. (2015) Human Cathelicidin Antimicrobial Protein 18 (hCAP18/LL-37) Is Increased in Foetal Membranes and Myometrium after Spon-taneous Labour and Delivery. Journal of Reproductive Immunology, 107, 31-42. [Google Scholar] [CrossRef] [PubMed]
[24] Chen, K.Q., Yoshimura, T., Gong, W.H., et al. (2021) Requirement of CRAMP for Mouse Macrophages to Eliminate Phagocytosed E. coli through an Autophagy Pathway. Journal of Cell Science, 134, jcs252148. [Google Scholar] [CrossRef] [PubMed]
[25] Torres-Juarez, F., Cardenas-Vargas, A., Montoya-Rosales, A., et al. (2015) LL-37 Immunomodulatory Activity during Mycobacterium tuberculosis Infection in Macrophages. Infection and Immun-ity, 83, 4495-4503. [Google Scholar] [CrossRef
[26] Rapala-Kozik, M., Bochenska, O., Zawrotniak, M., et al. (2015) Inacti-vation of the Antifungal and Immunomodulatory Properties of Human Cathelicidin LL-37 by Aspartic Proteases Pro-duced by the Pathogenic Yeast Candida albicans. Infection and Immunity, 83, 2518-2530. [Google Scholar] [CrossRef
[27] Peiser, L. and Gordon, S. (2001) The Function of Scavenger Receptors Expressed by Macrophages and Their Role in the Regulation of Inflammation. Microbes and Infection, 3, 149-159. [Google Scholar] [CrossRef
[28] Vandermeer, T.J., Menconi, M.J., Zhuang, J., et al. (1995) Protective Effects of a Novel 32-Amino Acid C-Terminal Fragment of CAP18 in Endotoxemic Pigs. Surgery, 117, 656-662. [Google Scholar] [CrossRef