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牙龈单核细胞趋化蛋白-1 诱导蛋白-1(MCPIP-1)和黏膜相关淋巴组织淋巴瘤易位蛋白 1(MALT-1)的定位和表达谱。

Localization and expression profiles of gingival monocyte chemoattractant protein-1-induced protein-1 (MCPIP-1) and mucosa-associated lymphoid tissue lymphoma translocation protein 1 (MALT-1).

机构信息

Department of Periodontology, Institute of Dentistry, University of Turku, Lemminkäisenkatu 2, 20520, Turku, Finland.

Department of Periodontology, Faculty of Dentistry, Istanbul University, Istanbul, Turkey.

出版信息

Clin Oral Investig. 2023 May;27(5):2065-2074. doi: 10.1007/s00784-023-05010-5. Epub 2023 Apr 3.

Abstract

OBJECTIVES

The purposes of this study were to localize monocyte chemoattractant protein-1-induced protein-1 (MCPIP-1) and its suppressor mucosa-associated lymphoid tissue lymphoma translocation protein 1 (MALT-1) in gingival tissues and to profile their protein expression levels in relation to the clinical inflammation, Porphyromonas gingivalis colonization, and interleukin (IL)-8 levels.

MATERIALS AND METHODS

Study samples were collected from two independent study populations: (1) Gingival tissues were collected from eight periodontally healthy individuals and eight periodontitis patients to localize MCPIP-1 and MALT-1 immunohistochemically, and (2) forty-one gingival tissue samples with marginal, mild, or moderate to severe inflammation were collected from 20 periodontitis patients to determine MCPIP-1 and MALT-1 levels using immunoblots, P. gingivalis levels with qPCR, P. gingivalis gingipain activities with fluorogenic substrates, and IL-8 levels with multiplex technique.

RESULTS

MCPIP-1 was detectable in the epithelium and in connective tissue, being especially prominent around the blood vessel walls in healthy periodontal tissues. MALT-1 was observed at all layers of gingival epithelium and especially around the accumulated inflammatory cells in connective tissue. No difference in gingival tissue MCPIP-1 and MALT-1 levels was observed in relation to the severity of gingival inflammation. MALT-1 levels were elevated (p = 0.023) with the increase in tissue P. gingivalis levels, and there was an association between MALT-1 and IL-8 levels (β = 0.054, p = 0.001).

CONCLUSIONS

Interactions of MALT-1 levels with gingival tissue P. gingivalis counts and IL-8 levels suggest that activation of MALT-1 can take part in P. gingivalis-regulated host immune responses.

CLINICAL RELEVANCE

Pharmacological targeting the crosstalk between immune response and MCPIP-1/MALT-1 may have benefits in periodontal treatment.

摘要

目的

本研究旨在定位单核细胞趋化蛋白-1 诱导蛋白-1(MCPIP-1)及其抑制剂黏膜相关淋巴组织淋巴瘤易位蛋白 1(MALT-1)在牙龈组织中的位置,并分析其蛋白表达水平与临床炎症、牙龈卟啉单胞菌定植和白细胞介素(IL)-8 水平的关系。

材料和方法

研究样本取自两个独立的研究人群:(1)从 8 名牙周健康个体和 8 名牙周炎患者中收集牙龈组织,通过免疫组织化学定位 MCPIP-1 和 MALT-1;(2)从 20 名牙周炎患者中收集 41 份边缘性、轻度或中重度炎症的牙龈组织样本,通过免疫印迹法测定 MCPIP-1 和 MALT-1 水平、qPCR 测定牙龈卟啉单胞菌水平、荧光底物测定牙龈卟啉单胞菌牙龈蛋白酶活性、多指标技术测定 IL-8 水平。

结果

MCPIP-1 在牙周组织健康时可在上皮组织和结缔组织中检测到,在血管壁周围尤为明显。MALT-1 在上皮组织的所有层中均可见,尤其是在结缔组织中积累的炎症细胞周围。牙龈组织中 MCPIP-1 和 MALT-1 水平与牙龈炎症的严重程度无关。MALT-1 水平随组织中牙龈卟啉单胞菌水平的升高而升高(p = 0.023),且 MALT-1 与 IL-8 水平之间存在关联(β=0.054,p=0.001)。

结论

MALT-1 水平与牙龈组织中牙龈卟啉单胞菌计数和 IL-8 水平的相互作用表明,MALT-1 的激活可能参与牙龈卟啉单胞菌调节的宿主免疫反应。

临床意义

针对免疫反应与 MCPIP-1/MALT-1 之间的相互作用进行药物靶向治疗可能有益于牙周治疗。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/70f9/10159971/0792311fe557/784_2023_5010_Fig1_HTML.jpg

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