Journal of Diagnostics Concepts & Practice ›› 2020, Vol. 19 ›› Issue (1): 44-49.doi: 10.16150/j.1671-2870.2020.01.010

• Original articles • Previous Articles     Next Articles

Effect of Haemophilus influenzae colonizing lower respiratory tract on airway inflammation and its signaling pathway in asthmatic mice

KANG Jianqiang1, DONG Yangyang2, YANG Ling2(), SONG Zhen3, FAN Jiaying3   

  1. 1. Geriatrics Department, Xinhua Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai 200092, China
    2. Shanghai Hongkou Sichuan North Road Sub District Community Health Service Center, Shanghai 200080, China
    3. Clinical Laboratory Medicine, Shanghai Jiao Tong University School of Medicine, Shanghai 200025, China
  • Received:2019-05-09 Online:2020-02-25 Published:2020-02-25
  • Contact: YANG Ling E-mail:yangling01@xinhuamed.com.cn

Abstract:

Objective: To observe the effect of Haemophilus influenzae colonizing lower respiratory tract on airway inflammation in asthmatic mice and study the related signaling pathway. Methods: Thirty-two C57/B6 mice were sensitized and challenged with ovalbumin (OVA) to establish a mice model of chronic asthma (AC group), and then half of them received intratracheal injection of Haemophilus influenza coated in agar beads to built a mice model of chronic asthma with airway Haemophilus influenza colonization (AS group). Besides, 16 C57/B6 mice were treated with intratracheal injection of Haemophilus influenza (NS group) and 16 C57/B6 mice received intratracheal injection of 0.9% NaCl (NC group). Sixty-four TLR4-/- mice were treated and grouped as C57/B6 mice. Mice including C57/B6 and TLR4-/- mice were sacrificed at 7 and 14 days after intratracheal injection, and serum tumor necrosis factor α(TNF-α) content, total number of cells in bronchoalveolar lavage fluid( BALF), and the expression of MyD88 and NF-κB in lung tissue were measured. The indice in AS group were compared with those in the control groups (AC, NS and NC) at corresponding time. Results: The serum level of TNF-α, total number of cells in BALF, and expression of MyD88 and NF-κB in lung tissue were higher in AS group than those in NC and NS group (both in C57/B6 mice and TLR4-/- mice). Compared with C57/B6 wild-type mice, TLR4-/- mice in AS group had lower levels of serum TNF-α, decreased numbers of cells in BALF, and down-regulated expression of MyD88 and NF-κB in lung tissue. Conclusions: Lower airway colonization with Haemophilus influenzae may aggravate airway inflammation of asthma by activating the TLR4-MyD88 pathway and promoting expression of NF-κB, which may be one of the important mechanisms of asthma.

Key words: Haemophilus influenza, Asthma, Airway inflammation, Signaling pathway

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