Human NELL‐1 Expressed in Unilateral Coronal Synostosis

K Dr. Ting, H Vastardis, JB Mulliken… - Journal of Bone and …, 1999 - academic.oup.com
K Dr. Ting, H Vastardis, JB Mulliken, C Soo, A Tieu, H Do, E Kwong, CN Bertolami…
Journal of Bone and Mineral Research, 1999academic.oup.com
Surgical correction of unilateral coronal synostosis offers a unique opportunity to examine
the molecular differences between an abnormal and a normal cranial suture. We isolated
and identified a cDNA fragment whose expression was up‐regulated in the premature fusing
and fused coronal sutures, as compared with normal coronal sutures. The nucleotide
sequence of the full‐length cDNA of this gene, human NELL‐1, has∼ 61% homology with
the chicken Nel gene. Both chicken Nel and human NELL‐1 are comprised of six epidermal …
Abstract
Surgical correction of unilateral coronal synostosis offers a unique opportunity to examine the molecular differences between an abnormal and a normal cranial suture. We isolated and identified a cDNA fragment whose expression was up‐regulated in the premature fusing and fused coronal sutures, as compared with normal coronal sutures. The nucleotide sequence of the full‐length cDNA of this gene, human NELL‐1, has ∼61% homology with the chicken Nel gene. Both chicken Nel and human NELL‐1 are comprised of six epidermal growth factor‐like repeats. The human NELL‐1 messages were localized primarily in the mesenchymal cells and osteoblasts at the osteogenic front, along the parasutural bone margins, and within the condensing mesenchymal cells of newly formed bone in sites of premature sutural fusion. Human multiorgan tissue mRNA blot showed that NELL‐1 was specifically expressed in fetal brain but not in fetal kidney, liver, or lung. We also showed that Nell‐1 was expressed in rat calvarial osteoprogenitor cells and was largely absent in rat tibiae and fibroblast cell cultures. In conclusion, our data suggest that the NELL‐1 gene is preferentially expressed in cranial intramembranous bone and neural tissue (both of neural crest cell origin) and is up‐regulated during unilateral premature closure of the coronal suture. The precise role of this gene is unknown.
Oxford University Press