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间充质基质细胞改善干燥综合征样疾病小鼠的唾液功能并减少淋巴细胞浸润。

Mesenchymal stromal cells improve salivary function and reduce lymphocytic infiltrates in mice with Sjögren's-like disease.

机构信息

Faculty of Dentistry, McGill University, Montreal, Quebec, Canada.

出版信息

PLoS One. 2012;7(6):e38615. doi: 10.1371/journal.pone.0038615. Epub 2012 Jun 7.

Abstract

BACKGROUND

Non-obese diabetic (NOD) mice develop Sjögren's-like disease (SS-like) with loss of saliva flow and increased lymphocytic infiltrates in salivary glands (SGs). There are recent reports using multipotent mesenchymal stromal cells (MSCs) as a therapeutic strategy for autoimmune diseases due to their anti-inflammatory and immunomodulatory capabilities. This paper proposed a combined immuno- and cell-based therapy consisting of: A) an injection of complete Freund's adjuvant (CFA) to eradicate autoreactive T lymphocytes, and B) transplantations of MSCs to reselect lymphocytes. The objective of this was to test the effectiveness of CD45(-)/TER119(-) cells (MSCs) in re-establishing salivary function and in reducing the number of lymphocytic infiltrates (foci) in SGs. The second objective was to study if the mechanisms underlying a decrease in inflammation (focus score) was due to CFA, MSCs, or CFA+MSCs combined.

METHODOLOGY/PRINCIPAL FINDINGS: Donor MSCs were isolated from bones of male transgenic eGFP mice. Eight week-old female NOD mice received one of the following treatments: insulin, CFA, MSC, or CFA+MSC (combined therapy). Mice were followed for 14 weeks post-therapy. CD45(-)/TER119(-) cells demonstrated characteristics of MSCs as they were positive for Sca-1, CD106, CD105, CD73, CD29, CD44, negative for CD45, TER119, CD11b, had high number of CFU-F, and differentiated into osteocytes, chondrocytes and adipocytes. Both MSC and MSC+CFA groups prevented loss of saliva flow and reduced lymphocytic infiltrations in SGs. Moreover, the influx of T and B cells decreased in all foci in MSC and MSC+CFA groups, while the frequency of Foxp3(+) (T(reg)) cell was increased. MSC-therapy alone reduced inflammation (TNF-α, TGF-β), but the combination of MSC+CFA reduced inflammation and increased the regenerative potential of SGs (FGF-2, EGF).

CONCLUSIONS/SIGNIFICANCE: The combined use of MSC+CFA was effective in both preventing saliva secretion loss and reducing lymphocytic influx in salivary glands.

摘要

背景

非肥胖型糖尿病(NOD)小鼠会发展为类干燥综合征(SS 样),表现为唾液流率降低和唾液腺(SGs)中淋巴细胞浸润增加。最近有报道称,多能间充质基质细胞(MSCs)具有抗炎和免疫调节功能,可作为治疗自身免疫性疾病的一种策略。本文提出了一种联合免疫和细胞的治疗方法,包括:A)注射完全弗氏佐剂(CFA)以消除自身反应性 T 淋巴细胞,和 B)移植 MSCs 以重新选择淋巴细胞。目的是测试 CD45(-)/TER119(-) 细胞(MSCs)在重建唾液功能和减少 SGs 中淋巴细胞浸润(灶)方面的有效性。第二个目的是研究炎症减少(灶评分)的机制是否归因于 CFA、MSCs 或 CFA+MSCs 的联合作用。

方法/主要发现:供体 MSCs 从雄性转基因 eGFP 小鼠的骨骼中分离出来。8 周龄雌性 NOD 小鼠接受以下治疗之一:胰岛素、CFA、MSC 或 CFA+MSC(联合治疗)。治疗后 14 周对小鼠进行跟踪观察。CD45(-)/TER119(-) 细胞表现出 MSC 的特征,因为它们对 Sca-1、CD106、CD105、CD73、CD29、CD44 呈阳性,对 CD45、TER119、CD11b 呈阴性,具有高数量的集落形成单位-F(CFU-F),并分化为成骨细胞、软骨细胞和脂肪细胞。MSC 和 MSC+CFA 组均防止唾液流率降低,并减少 SGs 中的淋巴细胞浸润。此外,MSC 和 MSC+CFA 组所有灶中 T 和 B 细胞的流入减少,而 Foxp3(+)(Treg)细胞的频率增加。单独的 MSC 治疗可降低炎症(TNF-α、TGF-β),但 MSC+CFA 的联合使用可降低炎症并增加 SGs 的再生潜能(FGF-2、EGF)。

结论/意义:MSC+CFA 的联合使用在防止唾液分泌损失和减少唾液腺中淋巴细胞浸润方面均有效。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bbe0/3369846/2504f8792e3b/pone.0038615.g001.jpg

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