Academic Journal

Characterization and partial purification of Candida albicans Secretory IL-12 Inhibitory Factor

التفاصيل البيبلوغرافية
العنوان: Characterization and partial purification of Candida albicans Secretory IL-12 Inhibitory Factor
المؤلفون: Chandra Jyotsna, Mukherjee Pranab K, Wang Mingyue, Lattif Ali, McCormick Thomas S, Ghannoum Mahmoud A
المصدر: BMC Microbiology, Vol 8, Iss 1, p 31 (2008)
بيانات النشر: BMC, 2008.
سنة النشر: 2008
المجموعة: LCC:Microbiology
مصطلحات موضوعية: Microbiology, QR1-502
الوصف: Abstract Background We have previously shown that supernatant from Candida albicans (CA) culture contains a Secretory Interleukin (IL)-12 Inhibitory Factor (CA-SIIF), which inhibits IL-12 production by human monocytes. However, the effect of CA-SIIF on secretion of other cytokines by monocytes is unknown, and detailed characterization of this factor has not been performed. Results In this study, we demonstrate that the IL-12 inhibitory activity of CA-SIIF was serum-independent, based on the reduction of IL-12 levels in monocytes stimulated under serum-independent conditions. The minimal inhibitory dose of CA-SIIF was found to be 200 μg/ml. Investigation of CA-SIIF's effect on macrophages IL-12 production in vitro and in vivo also showed that CA-SIIF inhibited IL-12 production by murine macrophages both in vitro (from 571 ± 24 pg/ml to 387 ± 87 pg/ml; P = 0.05) and in vivo (from 262 ± 6 pg/ml to 144 ± 30 pg/ml; P < 0.05). In addition to IL-12, cytokine array analysis revealed that CA-SIIF induced differential production of other cytokines also. In this regard, reduction in levels were observed for IL-8, IL-10, IL-13, monocyte chemoattractant protein (MCP)-1, MCP-2, macrophage inflammatory protein (MIP)-1, RANTES, etc. In contrast, levels of other chemokines e.g. MCP-4, MIF and MIP-3α (P < 0.05) were increased. We also found that CA-SIIF suppressed the maturation of human monocytes to dendritic cells (CD1a expression = 13 ± 3% vs 36 ± 2% of the control; P < 0.01). Next, to identify the biochemical nature of CA-SIIF, we separated this factor into a Concanavalin A (ConA)-binding glycoprotein fraction (CA-SIIF-GP) and a non-ConA-binding protein fraction (CA-SIIF-NGP) using ConA affinity chromatography. Both fractions were then tested for this inhibitory effect on human monocyte IL-12 production. CA-SIIF-GP produced a higher inhibitory effect on IL-12 production compared to CA-SIIF-NGP and CA-SIIF crude (P < 0.01), proving that CA-SIIF is a glycoprotein in nature. Conclusion CA-SIIF is a glycoprotein which exhibits serum-independent inhibition of IL-12 production from monocytes in vitro and in vivo, and also modulates differentiation of monocytes into dendritic cells. These results suggest important role for CA-SIIF in interactions of C. albicans with the host immune system.
نوع الوثيقة: article
وصف الملف: electronic resource
اللغة: English
تدمد: 1471-2180
Relation: http://www.biomedcentral.com/1471-2180/8/31; https://doaj.org/toc/1471-2180
DOI: 10.1186/1471-2180-8-31
URL الوصول: https://doaj.org/article/ac9a19b03f4b44808c3962b4e9a52351
رقم الانضمام: edsdoj.9a19b03f4b44808c3962b4e9a52351
قاعدة البيانات: Directory of Open Access Journals
الوصف
تدمد:14712180
DOI:10.1186/1471-2180-8-31