Fat Body Cells Are Motile and Actively Migrate to Wounds to Drive Repair and Prevent Infection.
Fat Body Cells Are Motile and Actively Migrate to Wounds to Drive Repair and Prevent Infection.
复制标题
脂肪体细胞是运动的,并积极迁移到伤口以驱动修复并防止感染。
DOI:
10.1016/j.devcel.2018.01.026
复制
发表时间:
2018-02-26
影响因子:
11.8
通讯作者:
Martin P
中科院分区:
文献类型:
--
作者:
Franz A;Wood W;Martin P
Adipocytes have many functions in various tissues beyond energy storage, including regulating metabolism, growth, and immunity. However, little is known about their role in wound healing. Here we use live imaging of fat body cells, the equivalent of vertebrate adipocytes in Drosophila, to investigate their potential behaviors and functions following skin wounding. We find that pupal fat body cells are not immotile, as previously presumed, but actively migrate to wounds using an unusual adhesion-independent, actomyosin-driven, peristaltic mode of motility. Once at the wound, fat body cells collaborate with hemocytes, Drosophila macrophages, to clear the wound of cell debris; they also tightly seal the epithelial wound gap and locally release antimicrobial peptides to fight wound infection. Thus, fat body cells are motile cells, enabling them to migrate to wounds to undertake several local functions needed to drive wound repair and prevent infections. Fat body cells actively migrate to wounds using a peristaltic mode of motility Fat body cells tightly seal the gap by forming lamellipodia around the wound margin Fat body cells collaborate with macrophages to clear wound debris Fat body cells locally release antimicrobial peptides at infected wounds Adipocytes and their fly equivalent, fat body cells, have been considered immotile, but Franz et al. now show the latter can actively migrate to wounds using a peristaltic-like “swimming” motility. Once there, they multitask to clear wound cell debris, plug the epithelial gap, and upregulate AMPs to prevent infection.
登录
查看更多内容
影响因子:
9.8
作者:
Grönke S;Müller G;Hirsch J;Fellert S;Andreou A;Haase T;Jäckle H;Kühnlein RP
通讯作者:
Kühnlein RP
DOI:
10.1083/jcb.201211039
发表时间:
2013-07-22
期刊:
The Journal of cell biology
影响因子:
--
作者:
Antunes M;Pereira T;Cordeiro JV;Almeida L;Jacinto A
通讯作者:
Jacinto A
影响因子:
4.6
作者:
Gates, Julie;Mahaffey, James P.;Peifer, Mark
通讯作者:
Peifer, Mark
影响因子:
4.6
作者:
Cherbas, L;Hu, X;Cherbas, P
通讯作者:
Cherbas, P
影响因子:
56.9
作者:
Delanoue, Renald;Meschi, Eleonora;Leopold, Pierre
通讯作者:
Leopold, Pierre