TY - JOUR
T1 - Piezo2 expressed in proprioceptive neurons is essential for skeletal integrity
AU - Assaraf, Eran
AU - Blecher, Ronen
AU - Heinemann-Yerushalmi, Lia
AU - Krief, Sharon
AU - Carmel Vinestock, Ron
AU - Biton, Inbal E.
AU - Brumfeld, Vlad
AU - Rotkopf, Ron
AU - Avisar, Erez
AU - Agar, Gabriel
AU - Zelzer, Elazar
N1 - Publisher Copyright: © 2020, The Author(s).
PY - 2020/6/23
Y1 - 2020/6/23
N2 - 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.
AB - 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.
UR - http://www.scopus.com/inward/record.url?scp=85086786557&partnerID=8YFLogxK
U2 - https://doi.org/10.1038/s41467-020-16971-6
DO - https://doi.org/10.1038/s41467-020-16971-6
M3 - مقالة
C2 - 32576830
SN - 2041-1723
VL - 11
JO - Nature Communications
JF - Nature Communications
IS - 1
M1 - 3168
ER -