C. Sahlberg et al., LAMININ GAMMA-2 EXPRESSION IS DEVELOPMENTALLY-REGULATED DURING MURINETOOTH MORPHOGENESIS AND IS INTENSE IN AMELOBLASTS, Journal of dental research, 77(8), 1998, pp. 1589-1596
Mutations in the laminin gamma 2 gene cause junctional epidermolysis b
ullosa, and enamel hypoplasias are frequently seen in these patients.
Laminin gamma 2 is one of the three polypeptide chains forming the bas
ement membrane glycoprotein laminin-5. We have localized the expressio
n of the laminin gamma 2 gene by in situ hybridization during mouse to
oth development from early morphogenesis to completion of crown develo
pment. The expression was restricted to epithelial cells. During the e
arly morphogenesis of the tooth germ, laminin gamma 2 was expressed by
the outer dental epithelium and by the stellate reticulum cells. No e
xpression was detected in the cells of the inner dental epithelium giv
ing rise to ameloblasts. The pre-ameloblasts remained negative during
the early bell stage, but, interestingly, expression was very prominen
tly upregulated as the cells. differentiated into ameloblasts. This up
regulation appeared to coincide with the start of enamel matrix secret
ion. The ameloblasts expressed laminin gamma 2 intensely throughout th
e period of active enamel deposition. The expression continued at a lo
wer level in the maturation-stage ameloblasts covering the enamel surf
ace. Immunolocalization of laminin-5 with polyclonal antibodies indica
ted that the protein formed a continuous lining at the basal surfaces
of the cells expressing the laminin gamma 2 transcripts. We suggest th
at the role of laminin-5 during enamel formation may be to strengthen
the anchorage of the ameloblasts to the enamel matrix, and that the pa
thogenesis of enamel hypoplasias in cases of laminin-5 mutations could
be associated with detachment of the ameloblast cell layer from the e
namel surface.