New! Sign up for our free email newsletter.
Science News
from research organizations

New knowledge on the development of asthma

Date:
June 26, 2019
Source:
Karolinska Institutet
Summary:
Researchers have studied which genes are expressed in overactive immune cells in mice with asthma-like inflammation of the airways. Their results suggest that the synthesis and breakdown of fats plays an important part in the process.
Share:
FULL STORY

Researchers at Karolinska Institutet in Sweden have studied which genes are expressed in overactive immune cells in mice with asthma-like inflammation of the airways. Their results, which are published in the journal Immunity, suggest that the synthesis and breakdown of fats plays an important part in the process.

The job of the human immune system is to read our environment and react to potentially harmful substances. In asthma, the immune system is overactive, causing inflammation in the lungs and symptoms such as coughing, wheezing and shortness of breath.

A kind of immune T cell called a Th2 cell plays a vital part in asthma-related inflammation, but the rarity of these cells and a lack of sensitivity technology has made these cells hard to study in any detail.

Researchers at Karolinska Institutet have now used a highly sensitive technique called single-cell RNA sequencing to analyse which genes are active in individual T cells. For the study, the team exposed mice to house dust mites, a common allergen to which most asthmatics are sensitive and which induces asthma-like lung inflammation. They then monitored gene expression in T cells before and after exposure to the allergens in the lymph glands to the point of inflammation in the lungs.

They found that in the mouse lung, the T cells express a unique profile of hundreds of genes, many of which are linked to how the cells make and break down fat. When they then gave mice a drug to block fat metabolism, the lung inflammation decreased relative to controls.

"Our results suggest that fats can help to aggravate the T-cell activated inflammation in the lungs that is seen in asthma," says the study's corresponding author Jonathan Coquet, researcher at the Department of Microbiology, Tumor and Cell Biology, Karolinska Institutet. "We now plan to systematically test the importance of the hundreds of uniquely expressed genes in order to find those that can trigger or prevent the development of the disease."

Another feature of the study was that when T cells reached the lungs from the lymph glands, they received signals that switched on the production of two powerful inflammatory substances: the cytokines interleukin 5 and 13. These cytokines are responsible for many of our normal asthma symptoms, such as respiratory tract inflammation, muscle contraction and mucus discharge.

"Our observation is that the T cells change a great deal over time and seem to undergo a kind of reprogramming in the lungs that makes them highly inflammatory," says Dr Coquet.


Story Source:

Materials provided by Karolinska Institutet. Note: Content may be edited for style and length.


Journal Reference:

  1. Christopher Andrew Tibbitt, Julian Mario Stark, Liesbet Martens, Junjie Ma, Jeff Eron Mold, Kim Deswarte, Ganna Oliynyk, Xiaogang Feng, Bart Norbert Lambrecht, Pieter De Bleser, Susanne Nylén, Hamida Hammad, Marie Arsenian Henriksson, Yvan Saeys, Jonathan Marie Coquet. Single-Cell RNA Sequencing of the T Helper Cell Response to House Dust Mites Defines a Distinct Gene Expression Signature in Airway Th2 Cells. Immunity, 2019; DOI: 10.1016/j.immuni.2019.05.014

Cite This Page:

Karolinska Institutet. "New knowledge on the development of asthma." ScienceDaily. ScienceDaily, 26 June 2019. <www.sciencedaily.com/releases/2019/06/190626160332.htm>.
Karolinska Institutet. (2019, June 26). New knowledge on the development of asthma. ScienceDaily. Retrieved December 21, 2024 from www.sciencedaily.com/releases/2019/06/190626160332.htm
Karolinska Institutet. "New knowledge on the development of asthma." ScienceDaily. www.sciencedaily.com/releases/2019/06/190626160332.htm (accessed December 21, 2024).

Explore More

from ScienceDaily

RELATED STORIES