Use of mir-155 in the preparation of medicines for preventing and treating acute lung injury
A composition and pulmonary hemorrhage technology, applied in the field of biomedicine, can solve problems such as expression defects and increased secretion
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Embodiment 1
[0070] Example 1. miR-155 knockout mice are resistant to Pristane-induced pulmonary hemorrhage
[0071] The inventors first detected the expression level of miR-155 in the Pristane-induced acute lung injury mouse model. It was found that after intraperitoneal injection of 0.5ml Pristane for two weeks, compared with the control group, the expression of miR-155 in the lung was significantly up-regulated (see figure 2 a-b).
[0072] In order to clarify the role of miR-155 in acute lung injury, the inventors used miR-155 gene knockout mice to conduct Pristane induction experiments. It was found that mice knocked out of miR-155 had significant resistance to pulmonary hemorrhage (20% of mice developed pulmonary hemorrhage), while normal C57 mice had a disease rate as high as 80% (see figure 2 d). Compared with controls, miR-155 KO mice had intact lung structures (see figure 2 c).
Embodiment 2
[0073] Example 2. Intervention of miR-155 in vivo can prevent the occurrence of Pristane-induced pulmonary hemorrhage
[0074] In order to further clarify the role of miR-155 in the process of lung injury, the inventors used miR-155 antagomir to conduct in vivo intervention experiments.
[0075] The results showed that mice injected with miR-155antagomir (miR-155anta) had significant resistance to Pristane-induced pulmonary hemorrhage ( image 3 a-b).
[0076] In order to verify the inhibitory efficiency of miR-155 antagomir, the inventors collected RNA from different tissues and performed quantitative analysis of miR-155. It was found that, at 14 days, the expression level of miR-155 in each tissue of the mice injected with miR-155antagomir was lower than that of the antagomir negative control group and the PBS group ( image 3 c). This shows that miR-155antagomir is effective, and the resistance of mice to pulmonary hemorrhage is indeed due to the absence of miR-155.
Embodiment 3
[0077] Example 3, miR-155 can promote the secretion of inflammatory factors in serum
[0078] It has been reported that miR-155, as a pro-inflammatory factor, can promote the expression of some inflammatory factors, such as IL-6 and TNF-a [14].
[0079] Therefore, the present inventors examined whether miR-155 deletion has an effect on the production of inflammatory cytokines in a Pristane-induced pulmonary hemorrhage model. On the 14th day of Pristane induction, different groups of serum were collected, and through the bioplex-cytokine suspension chip, the inventors found that some inflammatory factors, such as IL-1b, IL-6, TNF-a, IL-17, were induced by Pristane 14-day-old normal mice were significantly increased, while in miR-155KO mice, the expression levels of these factors were significantly reduced ( Figure 4 ).
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