Rapid re-synostosis following suturectomy in pediatric mice is age and location dependent

Christopher D. Hermann, Kelsey Lawrence, Rene Olivares-Navarrete, Joseph K. Williams, Robert E. Guldberg, Barbara D. Boyan, Zvi Schwartz

Research output: Contribution to journalArticle

4 Citations (Scopus)

Abstract

Craniosynostosis is the premature fusion of the cranial sutures early in development. If left untreated, craniosynostosis can lead to complications resulting from cranial deformities or increased intracranial pressure. The standard treatment involves calvarial reconstruction, which in many cases undergoes rapid re-synostosis. This requires additional surgical intervention that is associated with a high incidence of life threatening complications. To better understand this rapid healing, a pediatric mouse model of re-synostosis was developed and characterized. Defects (1.5. mm by 2.5. mm) over the posterior frontal suture were created surgically in weanling (21. days post-natal) and adolescent (50. days post-natal) C57Bl/6J mice. In addition, defects were created in the frontal bone lateral to the posterior frontal suture. The regeneration of bone in the defect was assessed using advanced image processing algorithms on micro-computed tomography scans. The genes associated with defect healing were assessed by real-time PCR of mRNA isolated from the tissue present in the defect. The results showed that the weanling mouse healed in a biphasic process with bone bridging the defect by post-operative (post-op) day 3 followed by an increase in the bone volume on day 14. In adolescent mice, there was a delay in bone bridging across the defect, and no subsequent increase in bone volume. No bridging of the defect by 14. days post-op was seen in identically sized defects placed lateral to the suture in both weanling and adolescent animals. This study demonstrates that bone regeneration in the cranium is both age and location dependent. Rapid and robust bone regeneration only occurred when the defect was created over the posterior frontal suture in immature weanling mice.

Original languageEnglish (US)
Pages (from-to)284-293
Number of pages10
JournalBone
Volume53
Issue number1
DOIs
StatePublished - Mar 2013

Fingerprint

Synostosis
Sutures
Bone Regeneration
Pediatrics
Bone and Bones
Craniosynostoses
Cranial Sutures
Frontal Bone
Intracranial Pressure
Skull
Real-Time Polymerase Chain Reaction
Tomography
Messenger RNA
Incidence
Genes

Keywords

  • Cranial defect
  • Craniosynostosis
  • Endochondral ossification
  • Micro-CT
  • Re-synostosis

ASJC Scopus subject areas

  • Physiology
  • Endocrinology, Diabetes and Metabolism
  • Histology

Cite this

Hermann, C. D., Lawrence, K., Olivares-Navarrete, R., Williams, J. K., Guldberg, R. E., Boyan, B. D., & Schwartz, Z. (2013). Rapid re-synostosis following suturectomy in pediatric mice is age and location dependent. Bone, 53(1), 284-293. https://doi.org/10.1016/j.bone.2012.11.019

Rapid re-synostosis following suturectomy in pediatric mice is age and location dependent. / Hermann, Christopher D.; Lawrence, Kelsey; Olivares-Navarrete, Rene; Williams, Joseph K.; Guldberg, Robert E.; Boyan, Barbara D.; Schwartz, Zvi.

In: Bone, Vol. 53, No. 1, 03.2013, p. 284-293.

Research output: Contribution to journalArticle

Hermann, CD, Lawrence, K, Olivares-Navarrete, R, Williams, JK, Guldberg, RE, Boyan, BD & Schwartz, Z 2013, 'Rapid re-synostosis following suturectomy in pediatric mice is age and location dependent', Bone, vol. 53, no. 1, pp. 284-293. https://doi.org/10.1016/j.bone.2012.11.019
Hermann CD, Lawrence K, Olivares-Navarrete R, Williams JK, Guldberg RE, Boyan BD et al. Rapid re-synostosis following suturectomy in pediatric mice is age and location dependent. Bone. 2013 Mar;53(1):284-293. https://doi.org/10.1016/j.bone.2012.11.019
Hermann, Christopher D. ; Lawrence, Kelsey ; Olivares-Navarrete, Rene ; Williams, Joseph K. ; Guldberg, Robert E. ; Boyan, Barbara D. ; Schwartz, Zvi. / Rapid re-synostosis following suturectomy in pediatric mice is age and location dependent. In: Bone. 2013 ; Vol. 53, No. 1. pp. 284-293.
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