We've updated our Privacy Policy to make it clearer how we use your personal data. We use cookies to provide you with a better experience. You can read our Cookie Policy here.

Advertisement

High Sugar Diet Alters Growth via Immune Signals

Sugar cubes arranged in a geometric pattern on a blue surface.
Credit: Cleo Beater / Pexels.
Read time: 1 minute

Diets rich in sugars and fats are associated with metabolic disorders such as insulin resistance, chronic inflammation, and diabetes. During development, these imbalances can have a particularly significant impact, as the body must coordinate growth, maturation, and hormone production.


A study conducted in Drosophila melanogaster, led by Dr. Sergio Juárez-Carreño and Dr. Marco Milán at IRB Barcelona, now reveals that macrophages-cells of the immune system-play a key role in this communication. In response to a high-sugar diet, these cells produce Dpp, a molecule homologous to human BMP2/4 proteins, which acts on the endocrine organ responsible for producing ecdysone, the steroid hormone that triggers metamorphosis.

Macrophages as nutritional status sensors

While macrophages are known for their role in the immune response, they also act as sensors of the body's physiological state. In contexts such as obesity and insulin resistance, for example, they contribute to metabolic inflammation and lipid accumulation in various tissues.


To this, a previously undescribed function can now be added, namely the modulation of hormone production during development. In larvae fed a high-sugar diet, macrophages increase the production of Dpp. This signal travels to the prothoracic gland and temporarily reduces ecdysone production, delaying the transition from larva to pupa.


"We knew that macrophages respond to metabolic stress, but not that they could regulate steroid hormone production. Our results show that these cells connect external nutritional signals with the physiology of the entire organism," explains Dr. Sergio Juárez-Carreño, first author of the study and currently a group leader at the Andalusian Center for Developmental Biology.

Buying time to grow

Under normal conditions, Drosophila larvae complete this developmental phase in about five days. On a high-sugar diet, the process is extended to six or seven days. According to the authors, this delay helps buffer the impact of that diet.


When the researchers blocked the Dpp signal produced by the macrophages, the larvae partially reduced the delay but reached a smaller size. This suggests that the immune response helps compensate for the impact of the high-sugar diet on growth, allowing the organism to buy time and reach adulthood in better condition.


"The immune system does not only respond to infections or damage. It also acts as an internal surveillance system, capable of adjusting the pace of development when nutritional conditions are sub-optimal," notes Dr. Marco Milán, ICREA researcher and head of the Development and Growth Control laboratory at IRB Barcelona.

Nutrition, hormones, and development

Drosophila melanogaster is a widely used model in biomedical research to study fundamental processes of development, metabolism, and hormonal regulation. In this system, the transition from larva to pupa makes it possible to analyze how steroid hormones coordinate major physiological changes during development. Furthermore, BMP proteins are evolutionarily conserved and have been linked to metabolic processes and insulin resistance in mammals.


Reference: Juarez-Carreño S, Milán M. A systemic role of macrophage-derived BMP2/4 homolog Dpp in inhibiting sterol hormone synthesis under dietary stress. Curr Biol. 2026;36(12):3165-3175.e4. doi: 10.1016/j.cub.2026.05.028

This article has been republished from the following materials. Note: material may have been edited for length and content. For further information, please contact the cited source. Our press release publishing policy can be accessed here.

Google News Preferred Source Add Technology Networks as a preferred Google source to see more of our trusted coverage.