Helminth protein enhances wound healing by inhibiting fibrosis and promoting tissue regeneration

被引:2
|
作者
Lothstein, Katherine E. [1 ]
Chen, Fei [1 ]
Mishra, Pankaj [1 ]
Smyth, Danielle J. [3 ]
Wu, Wenhui [1 ]
Lemenze, Alexander [2 ]
Kumamoto, Yosuke [2 ]
Maizels, Rick M. [3 ]
Gause, William C. [1 ]
机构
[1] Rutgers State Univ, Ctr Immun & Inflammat, New Jersey Med Sch, Dept Med, Newark, NJ 07103 USA
[2] Rutgers State Univ, Ctr Immun & Inflammat, Dept Pathol Immunol & Lab Med, New Jersey Med Sch, Newark, NJ USA
[3] Univ Glasgow, Wellcome Ctr Integrat Parasitol, Sch Infect & Immun, Glasgow, Scotland
基金
英国惠康基金;
关键词
TGF-BETA; TYPE-2; IMMUNITY; IN-VITRO; SKIN; CELLS; REPAIR; INFLAMMATION; SUPPRESSION; FIBROBLAST; CONTRIBUTE;
D O I
10.26508/lsa.202302249
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Skin wound healing due to full thickness wounds typically results in fibrosis and scarring, where parenchyma tissue is replaced with connective tissue. A major advance in wound healing research would be to instead promote tissue regeneration. Helminth parasites express excretory/secretory (ES) molecules, which can modulate mammalian host responses. One recently discovered ES protein, TGF-/3 mimic (TGM), binds the TGF-/3 receptor, though likely has other activities. Here, we demonstrate that topical administration of TGM under a Tegaderm bandage enhanced wound healing and tissue regeneration in an in vivo wound biopsy model. Increased restoration of normal tissue structure in the wound beds of TGM-treated mice was observed during mid- to late-stage wound healing. Both accelerated re-epithelialization and hair follicle regeneration were observed. Further analysis showed differential expansion of myeloid populations at different wound healing stages, suggesting recruitment and reprogramming of specific macrophage subsets. This study indicates a role for TGM as a potential therapeutic option for enhanced wound healing.
引用
收藏
页数:14
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