4.7 Article

Toll signalling promotes blastema cell proliferation during cricket leg regeneration via insect macrophages

期刊

DEVELOPMENT
卷 149, 期 8, 页码 -

出版社

COMPANY BIOLOGISTS LTD
DOI: 10.1242/dev.199916

关键词

Regeneration; Toll-related signalling; JAK/STAT signalling; Macrophages; Blastema; Gryllus bimaculatus

资金

  1. Ministry of Education, Culture, Sports, Science, and Technology of Japan [22124003, 15K06897, 18K06184]
  2. Grants-in-Aid for Scientific Research [15K06897, 22124003, 18K06184] Funding Source: KAKEN

向作者/读者索取更多资源

The study investigates the function of Toll-related molecules in leg regeneration of the two-spotted cricket Gryllus bimaculatus, suggesting that the Spz-Toll-related signaling in plasmatocytes promotes leg regeneration through blastema cell proliferation.
Hemimetabolous insects, such as the two-spotted cricket Gryllus bimaculatus, can recover lost tissues, in contrast to the limited regenerative abilities of human tissues. Following cricket leg amputation, the wound surface is covered by the wound epidermis, and plasmatocytes, which are insect macrophages, accumulate in the wound region. Here, we studied the function of Toll-related molecules identified by comparative RNA sequencing during leg regeneration. Of the 11 Toll genes in the Gryllus genome, expression of Toll2-1, Toll2-2 and Toll2-5 was upregulated during regeneration. RNA interference (RNAi) of Toll, Toll2-1, Toll2-2, Toll2-3 or Toll2-4 produced regeneration defects in more than 50% of crickets. RNAi of Toll2-2 led to a decrease in the ratio of S- and M-phase cells, reduced expression of JAK/STAT signalling genes, and reduced accumulation of plasmatocytes in the blastema. Depletion of plasmatocytes in crickets using clodronate also produced regeneration defects, as well as fewer proliferating cells in the regenerating legs. Plasmatocyte depletion also downregulated the expression of Toll and JAK/STAT signalling genes in the regenerating legs. These results suggest that Spz-Toll-related signalling in plasmatocytes promotes leg regeneration through blastema cell proliferation by regulating the Upd-JAK/STAT signalling pathway.

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