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Multi-organ phenotypes in mice lacking latent TGFß binding protein 2 (LTBP2).
Bodmer, Nicholas K; Knutsen, Russell H; Roth, Robyn A; Castile, Ryan M; Brodt, Michael D; Gierasch, Carrie M; Broekelmann, Thomas J; Gibson, Mark A; Haspel, Jeffrey A; Lake, Spencer P; Koenitzer, Jeffrey R; Brody, Steven L; Silva, Matthew J; Mecham, Robert P; Ornitz, David M.
Afiliação
  • Bodmer NK; Department of Developmental Biology, Washington University School of Medicine, St Louis, Missouri, USA.
  • Knutsen RH; Department of Cell Biology and Physiology, Washington University School of Medicine, St Louis, Missouri, USA.
  • Roth RA; Department of Cell Biology and Physiology, Washington University School of Medicine, St Louis, Missouri, USA.
  • Castile RM; Department of Cell Biology and Physiology, Washington University School of Medicine, St Louis, Missouri, USA.
  • Brodt MD; Department of Mechanical Engineering and Materials Science, Washington University School of Engineering, St Louis, Missouri, USA.
  • Gierasch CM; Department of Orthopedic Surgery, Washington University School of Medicine, St Louis, Missouri, USA.
  • Broekelmann TJ; Division of Pulmonary & Critical Care Medicine, Department of Medicine, Washington University School of Medicine, St Louis, Missouri, USA.
  • Gibson MA; Department of Cell Biology and Physiology, Washington University School of Medicine, St Louis, Missouri, USA.
  • Haspel JA; Discipline of Anatomy and Pathology, School of Medicine, University of Adelaide, Adelaide, South Australia, Australia.
  • Lake SP; Division of Pulmonary & Critical Care Medicine, Department of Medicine, Washington University School of Medicine, St Louis, Missouri, USA.
  • Koenitzer JR; Department of Mechanical Engineering and Materials Science, Washington University School of Engineering, St Louis, Missouri, USA.
  • Brody SL; Division of Pulmonary & Critical Care Medicine, Department of Medicine, Washington University School of Medicine, St Louis, Missouri, USA.
  • Silva MJ; Division of Pulmonary & Critical Care Medicine, Department of Medicine, Washington University School of Medicine, St Louis, Missouri, USA.
  • Mecham RP; Department of Orthopedic Surgery, Washington University School of Medicine, St Louis, Missouri, USA.
  • Ornitz DM; Department of Cell Biology and Physiology, Washington University School of Medicine, St Louis, Missouri, USA.
Dev Dyn ; 253(2): 233-254, 2024 Feb.
Article em En | MEDLINE | ID: mdl-37688792
ABSTRACT

BACKGROUND:

Latent TGFß binding protein-2 (LTBP2) is a fibrillin 1 binding component of the microfibril. LTBP2 is the only LTBP protein that does not bind any isoforms of TGFß, although it may interfere with the function of other LTBPs or interact with other signaling pathways.

RESULTS:

Here, we investigate mice lacking Ltbp2 (Ltbp2-/- ) and identify multiple phenotypes that impact bodyweight and fat mass, and affect bone and skin development. The alterations in skin and bone development are particularly noteworthy since the strength of these tissues is differentially affected by loss of Ltbp2. Interestingly, some tissues that express high levels of Ltbp2, such as the aorta and lung, do not have a developmental or homeostatic phenotype.

CONCLUSIONS:

Analysis of these mice show that LTBP2 has complex effects on development through direct effects on the extracellular matrix (ECM) or on signaling pathways that are known to regulate the ECM.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Proteínas de Transporte / Matriz Extracelular Limite: Animals Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Proteínas de Transporte / Matriz Extracelular Limite: Animals Idioma: En Ano de publicação: 2024 Tipo de documento: Article