4.6 Article

Integrin β2 and β3: Two plasmatocyte markers deepen our understanding of the development of plasmatocytes in the silkworm Bombyx mori

期刊

INSECT SCIENCE
卷 29, 期 6, 页码 1659-1671

出版社

WILEY
DOI: 10.1111/1744-7917.13045

关键词

Bombyx mori; hematopoiesis; MAPK; Erk; PI3K; Akt; plasmatocytes

资金

  1. National Natural Science Foundation of China [31802142]
  2. Doctoral Start-up Fund of the Southwest University [SWU120019]
  3. Fundamental Research Funds for the Central Universities [XDJK2019C089]
  4. China Postdoctoral Science Foundation [2019T120801, 2017M620408]

向作者/读者索取更多资源

Insect hemocytes, especially plasmatocytes, play important roles in the developmental stages, metamorphosis, and innate immunity. This study identified two molecular markers of plasmatocytes and investigated their role in plasmatocyte development. The results revealed that plasmatocytes are mainly generated and released by hematopoietic organs (HPOs) and their release is regulated by insulin-mediated signals and their downstream pathways. The PI3K/Akt pathway promotes hematopoiesis while the MAPK/Erk pathway negatively regulates the release of plasmatocytes. These findings enhance our understanding of insect hematopoiesis.
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 beta 2 and beta 3, 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.

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