Human Dermo-1 has attributes similar to twist in early bone development

Citation
Ms. Lee et al., Human Dermo-1 has attributes similar to twist in early bone development, BONE, 27(5), 2000, pp. 591-602
Citations number
44
Categorie Soggetti
Endocrynology, Metabolism & Nutrition","da verificare
Journal title
BONE
ISSN journal
87563282 → ACNP
Volume
27
Issue
5
Year of publication
2000
Pages
591 - 602
Database
ISI
SICI code
8756-3282(200011)27:5<591:HDHAST>2.0.ZU;2-Y
Abstract
Basic helix-loop-helix (bHLH) transcription factors are implicated in cell lineage determination and differentiation. Dermo-l encodes a bHLH transcrip tion factor that shares extensive homology with another bHLH transcription factor, Twist. We have cloned and characterized human Dermo-l from two diff erent hone cytoplasmic DNA (cDNA) libraries. Dermo-l mRNA and protein expre ssion were examined in human embryo and adult tissue sections. Dermo-l is e xpressed in a subset of mesodermally and ectodermally derived tissues. We f urther examined expression of Dermo-1/Twist in human tissues and cell lines . In addition, we observed Dermo-l expression in response to basic fibrobla st growth factor in osteoblastic cell lines, To evaluate the functionality of the human Dermo-l transcription factor in osteoblast metabolism, we made stable osteoblastic cell lines that over- and underexpress human Dermo-l, These cell lines were analyzed and compared with previously published data of similar cell lines transfected with Twist. Our results demonstrate that Dermo-l caused changes similar to Twist in the osteogenic properties of ost eoblastic cells, such as morphology, bone marker gene expression, and bioch emical response to cytokines, However, Dermo-l expression also has unique e ffects in regulating the mechanism of proliferation, on alkaline phosphatas e enzyme activity, and in temporal expression patterns. We speculate that e xpression of Twist and Dermo-l maintains cells in an osteoprogenitor or pre osteoblast-like state, respectively, and prevents premature or ectopic oste oblast differentiation. Therefore, Twist and Dermo-l must be sequentially d ownregulated in order to initiate the cascade of events responsible for ost eogenic cell differentiation. These results indicate that, during osteoblas t development, Dermo-l may inhibit osteoblast maturation and maintain cells in a preosteoblast phenotype by utilizing mechanisms similar but not ident ical to those utilized by Twist. (C) 2000 by Elsevier Science Inc. All righ ts reserved.