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Piezo2 expressed in proprioceptive neurons is essential for skeletal integrity.
Assaraf, Eran; Blecher, Ronen; Heinemann-Yerushalmi, Lia; Krief, Sharon; Carmel Vinestock, Ron; Biton, Inbal E; Brumfeld, Vlad; Rotkopf, Ron; Avisar, Erez; Agar, Gabriel; Zelzer, Elazar.
Afiliación
  • Assaraf E; Department of Molecular Genetics, Weizmann Institute of Science, Rehovot, 76100, Israel.
  • Blecher R; Department of Orthopedic Surgery, Assaf HaRofeh Medical Center, Sackler Faculty of Medicine, Tel Aviv University, Zerrifin, 70300, Israel.
  • Heinemann-Yerushalmi L; Department of Molecular Genetics, Weizmann Institute of Science, Rehovot, 76100, Israel.
  • Krief S; Department of Orthopedic Surgery, Assuta Ashdod University Hospital, Ashdod, 7747629, Israel.
  • Carmel Vinestock R; Ben Gurion University of the Negev, Beer-Sheva, 8410501, Israel.
  • Biton IE; Department of Molecular Genetics, Weizmann Institute of Science, Rehovot, 76100, Israel.
  • Brumfeld V; Department of Molecular Genetics, Weizmann Institute of Science, Rehovot, 76100, Israel.
  • Rotkopf R; Department of Molecular Genetics, Weizmann Institute of Science, Rehovot, 76100, Israel.
  • Avisar E; Department of Veterinary Resources, Weizmann Institute of Science, Rehovot, 76100, Israel.
  • Agar G; Department of Chemical Research Support, Weizmann Institute of Science, Rehovot, 76100, Israel.
  • Zelzer E; Bioinformatics Unit, Life Sciences Core Facilities, Weizmann Institute of Science, Rehovot, 76100, Israel.
Nat Commun ; 11(1): 3168, 2020 06 23.
Article en En | MEDLINE | ID: mdl-32576830
ABSTRACT
In humans, mutations in the PIEZO2 gene, which encodes for a mechanosensitive ion channel, were found to result in skeletal abnormalities including scoliosis and hip dysplasia. Here, we show in mice that loss of Piezo2 expression in the proprioceptive system recapitulates several human skeletal abnormalities. While loss of Piezo2 in chondrogenic or osteogenic lineages does not lead to human-like skeletal abnormalities, its loss in proprioceptive neurons leads to spine malalignment and hip dysplasia. To validate the non-autonomous role of proprioception in hip joint morphogenesis, we studied this process in mice mutant for proprioceptive system regulators Runx3 or Egr3. Loss of Runx3 in the peripheral nervous system, but not in skeletal lineages, leads to similar joint abnormalities, as does Egr3 loss of function. These findings expand the range of known regulatory roles of the proprioception system on the skeleton and provide a central component of the underlying molecular mechanism, namely Piezo2.
Asunto(s)

Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Propiocepción / Canales Iónicos / Anomalías Musculoesqueléticas / Sistema Musculoesquelético / Neuronas Tipo de estudio: Prognostic_studies Límite: Animals Idioma: En Revista: Nat Commun Asunto de la revista: BIOLOGIA / CIENCIA Año: 2020 Tipo del documento: Article País de afiliación: Israel

Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Propiocepción / Canales Iónicos / Anomalías Musculoesqueléticas / Sistema Musculoesquelético / Neuronas Tipo de estudio: Prognostic_studies Límite: Animals Idioma: En Revista: Nat Commun Asunto de la revista: BIOLOGIA / CIENCIA Año: 2020 Tipo del documento: Article País de afiliación: Israel