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Vegfc-expressing cells form heterotopic bone after musculoskeletal injury.
Vishlaghi, Neda; Guo, Lei; Griswold-Wheeler, Danielle; Sun, Yuxiao; Booker, Cori; Crossley, Janna L; Bancroft, Alec C; Juan, Conan; Korlakunta, Sneha; Ramesh, Sowmya; Pagani, Chase A; Xu, Lin; James, Aaron W; Tower, Robert J; Dellinger, Michael; Levi, Benjamin.
Afiliación
  • Vishlaghi N; Department of Surgery, University of Texas Southwestern, Dallas, TX, USA.
  • Guo L; Department of Population and Data Sciences, University of Texas Southwestern, Dallas, TX, USA.
  • Griswold-Wheeler D; Department of Surgery, University of Texas Southwestern, Dallas, TX, USA.
  • Sun Y; Department of Surgery, University of Texas Southwestern, Dallas, TX, USA.
  • Booker C; Department of Surgery, University of Texas Southwestern, Dallas, TX, USA.
  • Crossley JL; Department of Surgery, University of Texas Southwestern, Dallas, TX, USA.
  • Bancroft AC; Department of Surgery, University of Texas Southwestern, Dallas, TX, USA.
  • Juan C; Department of Surgery, University of Texas Southwestern, Dallas, TX, USA.
  • Korlakunta S; Department of Surgery, University of Texas Southwestern, Dallas, TX, USA.
  • Ramesh S; Department of Pathology, Johns Hopkins University, Baltimore, MD, USA.
  • Pagani CA; Department of Surgery, University of Texas Southwestern, Dallas, TX, USA.
  • Xu L; Department of Population and Data Sciences, University of Texas Southwestern, Dallas, TX, USA.
  • James AW; Department of Pathology, Johns Hopkins University, Baltimore, MD, USA.
  • Tower RJ; Department of Surgery, University of Texas Southwestern, Dallas, TX, USA.
  • Dellinger M; Department of Surgery, University of Texas Southwestern, Dallas, TX, USA. Electronic address: michael.dellinger@utsouthwestern.edu.
  • Levi B; Department of Surgery, University of Texas Southwestern, Dallas, TX, USA. Electronic address: benjamin.levi@utsouthwestern.edu.
Cell Rep ; 43(4): 114049, 2024 Apr 23.
Article en En | MEDLINE | ID: mdl-38573853
ABSTRACT
Heterotopic ossification (HO) is a challenging condition that occurs after musculoskeletal injury and is characterized by the formation of bone in non-skeletal tissues. While the effect of HO on blood vessels is well established, little is known about its impact on lymphatic vessels. Here, we use a mouse model of traumatic HO to investigate the relationship between HO and lymphatic vessels. We show that injury triggers lymphangiogenesis at the injury site, which is associated with elevated vascular endothelial growth factor C (VEGF-C) levels. Through single-cell transcriptomic analyses, we identify mesenchymal progenitor cells and tenocytes as sources of Vegfc. We demonstrate by lineage tracing that Vegfc-expressing cells undergo osteochondral differentiation and contribute to the formation of HO. Last, we show that Vegfc haploinsufficiency results in a nearly 50% reduction in lymphangiogenesis and HO formation. These findings shed light on the complex mechanisms underlying HO formation and its impact on lymphatic vessels.
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Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Osificación Heterotópica / Factor C de Crecimiento Endotelial Vascular / Linfangiogénesis / Células Madre Mesenquimatosas Límite: Animals Idioma: En Revista: Cell Rep Año: 2024 Tipo del documento: Article País de afiliación: Estados Unidos

Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Osificación Heterotópica / Factor C de Crecimiento Endotelial Vascular / Linfangiogénesis / Células Madre Mesenquimatosas Límite: Animals Idioma: En Revista: Cell Rep Año: 2024 Tipo del documento: Article País de afiliación: Estados Unidos