Integrin β2 and β3: Two plasmatocyte markers deepen our understanding of the development of plasmatocytes in the silkworm Bombyx mori.
Kui ZhangJingjing SuXin HuXiaomin YanSiyuan ChenChongyang LiGuangzhao PanHongbo ChangWenli TianMuhammad Nadeem AbbasHong-Juan CuiPublished in: Insect science (2022)
Insect hemocytes play important biological roles at developmental stages, metamorphosis, and innate immunity. As one of the most abundant cell types, plasmatocytes can participate in various innate immune responses, especially in encapsulation and node formation. Here, 2 molecular markers of plasmatocytes, consisting of integrin β2 and β3, were identified and used to understand the development of plasmatocytes. Plasmatocytes are widely distributed in the hematopoietic system, including circulating hemolymph and hematopoietic organs (HPOs). HPOs constantly release plasmatocytes with high proliferative activity in vitro; removal of HPOs leads to a dramatic reduction in the circulating plasmatocytes, and the remaining plasmatocytes gradually lose their ability to proliferate in vivo. Our results demonstrated that the release of plasmatocytes from HPOs is regulated by insulin-mediated signals and their downstream pathways, including PI3K/Akt and MAPK/Erk signals. The insulin/PI3K/Akt signaling pathway can significantly irritate the hematopoiesis, and its inhibitor LY294002 could inhibit the hemocytes discharged from HPOs. While the insulin/MAPK/Erk signaling pathway plays a negative regulatory role, inhibiting its activity with U0126 can markedly promote the discharge of plasmatocytes from HPOs. Our results indicate that the circulating plasmatocytes are mainly generated and discharged by HPOs. This process is co-regulated by the PI3K/Akt and MAPK/Erk signals in an antagonistic manner to adjust the dynamic balance of the hemocytes. These findings can enhance our understanding of insect hematopoiesis.
Keyphrases
- pi k akt
- signaling pathway
- cell cycle arrest
- cell proliferation
- immune response
- induced apoptosis
- type diabetes
- epithelial mesenchymal transition
- bone marrow
- lymph node
- transcription factor
- toll like receptor
- adipose tissue
- metabolic syndrome
- glycemic control
- single cell
- cell death
- mesenchymal stem cells
- inflammatory response
- insulin resistance
- single molecule
- aedes aegypti