TY - JOUR
T1 - Coordinated tether formation in anatomically distinct mice growth centers is dependent on a functional vitamin D receptor and is tightly linked to three-dimensional tissue morphology
AU - Lee, Christopher S.D.
AU - Chen, Jida
AU - Wang, Yun
AU - Williams, Joseph K.
AU - Ranly, Don M.
AU - Schwartz, Zvi
AU - Boyan, Barbara D.
N1 - Funding Information:
This research was supported by grants from the Price Gilbert, Jr. Foundation , Children's Healthcare of Atlanta , the Georgia Tech/Emory Center for the Engineering of Living Tissues ( NSF EEC 9731643 ), and the National Science Foundation Graduate Research Fellowship (Lee). The authors thank Dr. Robert Guldberg and Angela Lin for their assistance in developing a protocol to evaluate tether formation in the synchondrosis and Chris Hermann for his assistance in isolating cranial bases from mice.
Copyright:
Copyright 2012 Elsevier B.V., All rights reserved.
PY - 2011/9
Y1 - 2011/9
N2 - Bone bridges linking the epiphysis and metaphysis termed "tethers" have been found in the femoral growth plates of C57Bl/6 mice and are disrupted when the vitamin D receptor (VDR) is ablated. It is unknown if tethers are found in other growth centers, if they are regulated in a comparable manner, or if they have a functional role in skeletal development or stability. To address this, distal femoral growth plates (GPs) and spheno-occipital synchondroses (SOSs) of wild-type C57Bl/6 mice from 2 to 15weeks of age were analyzed using μCT scans. The GPs and SOSs of VDR+/+ and VDR-/- mice fed regular or rescue diets to restore mineral homeostasis until 10weeks of age were also scanned. Tethers in GPs and SOSs both thickened and accumulated in number as these growth centers decreased in size. Ablating the VDR made GPs and SOSs rachitic and nearly eliminated tether formation. Rescue diets restored the volume of both growth centers but only partially restored growth center thickness and tether formation, suggesting that lα,25-dihydroxy vitamin D 3 partially regulates tether formation in these growth centers via its receptor. In VDR+/+ mice 2-15weeks in age, growth center thickness was inversely correlated to animal weight whereas tether phenotype (tether volume/growth center volume, tether number/mm, tether width, tether spacing) was significantly related to animal weight. In both 2-15week old VDR+/+ and 10week old VDR+/+ and VDR-/- mice on normal and rescue diets, tether phenotype (tether number/mm, tether spacing) had strikingly similar relationships to growth center thickness. These results show that tethers are present in growth centers in different anatomic and undergo developmental changes in a comparable manner; in both sites, VDR-regulated tether formation is strongly linked to growth center morphology; and tether formation is associated with body weight, suggesting a role in maintaining growth plate stability during growth.
AB - Bone bridges linking the epiphysis and metaphysis termed "tethers" have been found in the femoral growth plates of C57Bl/6 mice and are disrupted when the vitamin D receptor (VDR) is ablated. It is unknown if tethers are found in other growth centers, if they are regulated in a comparable manner, or if they have a functional role in skeletal development or stability. To address this, distal femoral growth plates (GPs) and spheno-occipital synchondroses (SOSs) of wild-type C57Bl/6 mice from 2 to 15weeks of age were analyzed using μCT scans. The GPs and SOSs of VDR+/+ and VDR-/- mice fed regular or rescue diets to restore mineral homeostasis until 10weeks of age were also scanned. Tethers in GPs and SOSs both thickened and accumulated in number as these growth centers decreased in size. Ablating the VDR made GPs and SOSs rachitic and nearly eliminated tether formation. Rescue diets restored the volume of both growth centers but only partially restored growth center thickness and tether formation, suggesting that lα,25-dihydroxy vitamin D 3 partially regulates tether formation in these growth centers via its receptor. In VDR+/+ mice 2-15weeks in age, growth center thickness was inversely correlated to animal weight whereas tether phenotype (tether volume/growth center volume, tether number/mm, tether width, tether spacing) was significantly related to animal weight. In both 2-15week old VDR+/+ and 10week old VDR+/+ and VDR-/- mice on normal and rescue diets, tether phenotype (tether number/mm, tether spacing) had strikingly similar relationships to growth center thickness. These results show that tethers are present in growth centers in different anatomic and undergo developmental changes in a comparable manner; in both sites, VDR-regulated tether formation is strongly linked to growth center morphology; and tether formation is associated with body weight, suggesting a role in maintaining growth plate stability during growth.
KW - 1,25-dihydroxy vitamin D3
KW - Bone development
KW - Growth plate
KW - Micro-computed tomography (microCT)
KW - Rickets
KW - Synchondrosis
KW - Tethers
KW - Vitamin D receptor knockout mice (VDR-/-)
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U2 - 10.1016/j.bone.2011.05.004
DO - 10.1016/j.bone.2011.05.004
M3 - Article
C2 - 21601024
AN - SCOPUS:79960608557
SN - 8756-3282
VL - 49
SP - 419
EP - 427
JO - Bone
JF - Bone
IS - 3
ER -