Sfrp4 expression in thyroxine treated calvarial cells

• Published in: Life sciences (1973) Vol. 311; no. Pt A; p. 121158
• Main Authors: Durham, Emily L., Grey, Zachary J., Black, Laurel, Howie, R. Nicole, Barth, Jeremy L., Lee, Beth S., Cray, James J.
• Format: Journal Article
• Language: English
• Published: Netherlands Elsevier Inc 15.12.2022
• Subjects: Alkaline Phosphatase - metabolism; Animals; EMSA; Mice; mRNA; Osteoblasts - metabolism; Osteogenesis; Osteogenesis - genetics; Protein; Proto-Oncogene Proteins - metabolism; Sfrp4; Thyroxine; Thyroxine - metabolism; Wnt Signaling Pathway - genetics; Sfrp4; mRNA; EMSA; Osteogenesis; Protein; Thyroxine
• ISSN: 0024-3205; 1879-0631
• DOI: 10.1016/j.lfs.2022.121158

Evidence suggests alterations of thyroid hormone levels can disrupt normal bone development. Most data suggest the major targets of thyroid hormones to be the Htra1/Igf1 pathway. Recent discovery by our group suggests involvement of targets WNT pathway, specifically overexpression of antagonist Sfrp4 in the presence of exogenous thyroid hormone. Here we aimed to model these interactions in vitro using primary and isotype cell lines to determine if thyroid hormone drives increased Sfrp4 expression in cells relevant to craniofacial development. Transcriptional profiling, bioinformatics interrogation, protein and function analyses were used. Affymetrix transcriptional profiling found Sfrp4 overexpression in primary cranial suture derived cells stimulated with thyroxine in vitro. Interrogation of the SFRP4 promoter identified multiple putative binding sites for thyroid hormone receptors. Experimentation with several cell lines demonstrated that thyroxine treatment induced Sfrp4 expression, demonstrating that Sfrp4 mRNA and protein levels are not tightly coupled. Transcriptional and protein analyses demonstrate thyroid hormone receptor binding to the proximal promoter of the target gene Sfrp4 in murine calvarial pre-osteoblasts. Functional analysis after thyroxine hormone stimulation for alkaline phosphatase activity shows that pre-osteoblasts increase alkaline phosphatase activity compared to other cell types, suggesting cell type susceptibility. Finally, we added recombinant SFRP4 to pre-osteoblasts in combination with thyroxine treatment and observed a significant decrease in alkaline phosphatase positivity. Taken together, these results suggest SFRP4 may be a key regulatory molecule that prevents thyroxine driven osteogenesis. These data corroborate clinical findings indicating a potential for SFRP4 as a diagnostic or therapeutic target for hyperostotic craniofacial disorders.