Baicalin attenuates inflammation in mice with OVA-induced asthma by inhibiting NF-B and suppressing CCR7/CCL19/CCL21

被引:59
|
作者
Liu, Jiaqi [1 ,2 ]
Wei, Ying [1 ,2 ]
Luo, Qingli [1 ,2 ]
Xu, Fei [1 ,2 ]
Zhao, Zhengxiao [1 ,2 ]
Zhang, Hongying [1 ,2 ]
Lu, Linwei [1 ,2 ]
Sun, Jing [1 ,2 ]
Liu, Feng [1 ,2 ]
Du, Xin [1 ,2 ]
Li, Mihui [1 ,2 ]
Wei, Kai [1 ,2 ]
Dong, Jingcheng [1 ,2 ]
机构
[1] Fudan Univ, Huashan Hosp, Dept Integrat Med, 12 Middle Urumqi Rd, Shanghai 200040, Peoples R China
[2] Fudan Univ, Inst Integrated Tradit Chinese & Western Med, Shanghai 200040, Peoples R China
基金
中国国家自然科学基金;
关键词
asthma; baicalin; airway inflammation; CC chemokine receptor 7; CCL19; CCL21; nuclear factor-kappa B; CHEMOKINE RECEPTOR CCR7; AIRWAY SMOOTH-MUSCLE; NECROSIS-FACTOR-ALPHA; DENDRITIC CELLS; TNF-ALPHA; ALLERGIC INFLAMMATION; UP-REGULATION; EXPRESSION; DISEASE; ACTIVATION;
D O I
10.3892/ijmm.2016.2743
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Baicalin, extracted and purified from the Chinese medicinal plant, Scutellaria baicalensis Georgi (Huang qin in Chinese), exhibits potent anti-inflammatory activity against asthma. However, it remains unknown whether baicalin inhibits the activity of CC chemokine receptor 7 (CCR7) and its ligands, which are crucial for the initiation of airway inflammation. In the present study, we investigated the effects of baicalin on CCR7 and its ligands, CCL19 and CCL21, as well as on the nuclear factor-B (NF-B) pathway in a mouse model of asthma. A mouse model of acute asthma was established by exposing the mice to ovalbumin (OVA) (by intraperitoneal injection and inhalational challenge). Within 24 h of the final OVA challenge, lung function was detected by direct airway resistance analysis. Lung tissues were examined for pathological changes. Inflammatory cell counts in bronchoalveolar lavage fluid (BALF) were assessed. ELISA was utilized to evaluate the OVA-IgE, CCL19 and CCL21 levels in BALF. The interleukin (IL)-6 and tumor necrosis factor (TNF)- levels in serum were also detected by ELISA. The protein expression levels of CCR7, as well as that of phosphorylated IB (p-IB) and phosphorylated p65 (p-p65) were determined by western blot analysis and RT-qPCR was used to determine the CCR7 mRNA levels. Our data demonstrated that the oral administration of baicalin significantly improved pulmonary function and attenuated inflammatory cell infiltration into the lungs. Baicalin also decreased the levels of OVA-IgE, IL-6, TNF- and CCR7, as well as those of its ligand, CCL19; the levels of NF-B were also markedly suppressed by baicalin. The CCR7 mRNA level was substantially decreased. Our results thus suggest that baicalin exerts an inhibitory effect on airway inflammation, and this effect may be associated with the inhibition of CCR7 and CCL19/CCL21, which may provide new mechanistic insight into the anti-inflammatory effects of baicalin.
引用
收藏
页码:1541 / 1548
页数:8
相关论文
共 30 条
  • [1] Cloning and pharmacological characterization of CCR7, CCL21 and CCL19 from Macaca fascicularis
    Moxley, Rachel
    Day, Elizabeth
    Brown, Kate
    Mahnke, Marion
    Zurini, Mauro
    Schmitz, Rita
    Jones, Carol E.
    Jarai, Gabor
    EUROPEAN JOURNAL OF PHARMACEUTICAL SCIENCES, 2009, 37 (3-4) : 264 - 271
  • [2] Chemokines and common variable immunodeficiency; possible contribution of CCL19, CCL21 and CCR7 to immune dysregulation
    Fevang, B.
    Yndestad, A.
    Damas, J. K.
    Halvorsen, B.
    Holm, A. M.
    Beiske, K.
    Aukrust, P.
    Froland, S. S.
    CLINICAL AND EXPERIMENTAL IMMUNOLOGY, 2009, 158 (02) : 237 - 245
  • [3] Fluorescently Tagged CCL19 and CCL21 to Monitor CCR7 and ACKR4 Functions
    Purvanov, Vladimir
    Matti, Christoph
    Samson, Guerric P. B.
    Kindinger, Ilona
    Legler, Daniel F.
    INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES, 2018, 19 (12)
  • [4] Contribution of Homeostatic Chemokines CCL19 and CCL21 and Their Receptor CCR7 to Coronary Artery Disease
    Cai, Wenzhi
    Tao, Jie
    Zhang, Xiaolin
    Tian, Xiaoxiang
    Liu, Tengfei
    Feng, Xueyao
    Bai, Jing
    Yan, Chenghui
    Han, Yaling
    ARTERIOSCLEROSIS THROMBOSIS AND VASCULAR BIOLOGY, 2014, 34 (09) : 1933 - 1941
  • [5] Expression of duck CCL19 and CCL21 and CCR7 receptor in lymphoid and influenza-infected tissues
    Fleming-Canepa, Ximena
    Brusnyk, Craig
    Aldridge, Jerry R.
    Ross, Katherine L.
    Moon, Debra
    Wang, Dong
    Xia, Jianguo
    Barber, Megan R. W.
    Webster, Robert G.
    Magor, Katharine E.
    MOLECULAR IMMUNOLOGY, 2011, 48 (15-16) : 1950 - 1957
  • [6] A myriad of functions and complex regulation of the CCR7/CCL19/CCL21 chemokine axis in the adaptive immune system
    Comerford, Iain
    Harata-Lee, Yuka
    Bunting, Mark D.
    Gregor, Carly
    Kara, Ervin E.
    McColl, Shaun R.
    CYTOKINE & GROWTH FACTOR REVIEWS, 2013, 24 (03) : 269 - 283
  • [7] Central Nervous System and Peripheral Expression of CCL19, CCL21 and Their Receptor CCR7 in Experimental Model of Multiple Sclerosis
    Bielecki, Bartosz
    Jatczak-Pawlik, Izabela
    Wolinski, Pawel
    Bednarek, Andrzej
    Glabinski, Andrzej
    ARCHIVUM IMMUNOLOGIAE ET THERAPIAE EXPERIMENTALIS, 2015, 63 (05) : 367 - 376
  • [8] Biased Signaling of CCL21 and CCL19 Does Not Rely on N-Terminal Differences, but Markedly on the Chemokine Core Domains and Extracellular Loop 2 of CCR7
    Jorgensen, Astrid S.
    Larsen, Olav
    Uetz-von Allmen, Edith
    Luckmann, Michael
    Legler, Daniel F.
    Frimurer, Thomas M.
    Veldkamp, Christopher T.
    Hjorto, Gertrud M.
    Rosenkilde, Mette M.
    FRONTIERS IN IMMUNOLOGY, 2019, 10
  • [9] The expression of chemokines CCL19, CCL21 and their receptor CCR7 in oral squamous cell carcinoma and its relevance to cervical lymph node metastasis
    Oliveira-Neto, Helenisa Helena
    Chaves de Souza, Pedro Paulo
    Barbosa da Silva, Marcio Roberto
    Mendonca, Elismauro Francisco
    Silva, Tarcilia Aparecida
    Batista, Aline Carvalho
    TUMOR BIOLOGY, 2013, 34 (01) : 65 - 70
  • [10] The role of CCL21/CCR7 chemokine axis in breast cancer-induced lymphangiogenesis
    Tutunea-Fatan, Elena
    Majumder, Mousumi
    Xin, Xiping
    Lala, Peeyush K.
    MOLECULAR CANCER, 2015, 14