Yun-Sil Lee1, Se-Jin Lee1. 1. Department of Molecular Biology and Genetics, Johns Hopkins University School of Medicine, 725 North Wolfe Street, PCTB 803, Baltimore, MD 21205, USA.
Abstract
PURPOSE: Growth and differentiation factor-11 (GDF-11) is a TGF-β family member that plays important regulatory roles in development of multiple tissues which include axial skeletal patterning, palatal closure, and tooth formation. Proteins that have been identified as GDF-11 inhibitors include GDF-associated serum protein-1 (GASP-1) and GASP-2. Recently, we found that mice genetically engineered to lack both Gasp1 and Gdf11 have an increased frequency of cleft palate. The goal of this study was to investigate the roles of GDF-11 and its inhibitors, GASP-1 and GASP-2, during dental and craniofacial development and growth. METHODS: Mouse genetic studies were used in this study. Homozygous knockout mice for Gasp1 (Gasp1-/- ) and Gasp2 (Gasp2-/- ) were viable and fertile, but Gdf11 homozygous knockout (Gdf11-/- ) mice died within 24 hours after birth. The effect of either Gasp1 or Gasp2 deletion in Gdf11-/- mice during embryogenesis was evaluated in Gasp1-/-;Gdf11-/- and Gasp2-/-;Gdf11-/- mouse embryos at 18.5 days post-coitum (E18.5). For the analysis of adult tissues, we used Gasp1-/-;Gdf11+/- and Gasp2-/-;Gdf11+/- mice to evaluate the potential haploinsufficiency of Gdf11 in Gasp1-/- and Gasp2-/- mice. RESULTS: Although Gasp2 expression decreased after E10.5, Gasp1 expression was readily detected in various ectodermal tissues at E17.5, including hair follicles, epithelium in nasal cavity, retina, and developing tooth buds. Interestingly, Gasp1-/- ;Gdf11-/- mice had abnormal formation of lower incisors: tooth buds for lower incisors were under-developed or missing. Although Gdf11+/- mice were viable and had mild transformations of the axial skeleton, no specific defects in the craniofacial development have been observed in Gdf11+/- mice. However, loss of Gasp1 in Gdf11+/- mice occasionally resulted in small and abnormally shaped auricles. CONCLUSIONS: These findings suggest that both GASP-1 and GDF-11 play important roles in dental and craniofacial development both during embryogenesis and in adult tissues.
PURPOSE:Growth and differentiation factor-11 (GDF-11) is a TGF-β family member that plays important regulatory roles in development of multiple tissues which include axial skeletal patterning, palatal closure, and tooth formation. Proteins that have been identified as GDF-11 inhibitors include GDF-associated serum protein-1 (GASP-1) and GASP-2. Recently, we found that mice genetically engineered to lack both Gasp1 and Gdf11 have an increased frequency of cleft palate. The goal of this study was to investigate the roles of GDF-11 and its inhibitors, GASP-1 and GASP-2, during dental and craniofacial development and growth. METHODS:Mouse genetic studies were used in this study. Homozygous knockout mice for Gasp1 (Gasp1-/- ) and Gasp2 (Gasp2-/- ) were viable and fertile, but Gdf11 homozygous knockout (Gdf11-/- ) mice died within 24 hours after birth. The effect of either Gasp1 or Gasp2 deletion in Gdf11-/- mice during embryogenesis was evaluated in Gasp1-/-;Gdf11-/- and Gasp2-/-;Gdf11-/- mouse embryos at 18.5 days post-coitum (E18.5). For the analysis of adult tissues, we used Gasp1-/-;Gdf11+/- and Gasp2-/-;Gdf11+/- mice to evaluate the potential haploinsufficiency of Gdf11 in Gasp1-/- and Gasp2-/- mice. RESULTS: Although Gasp2 expression decreased after E10.5, Gasp1 expression was readily detected in various ectodermal tissues at E17.5, including hair follicles, epithelium in nasal cavity, retina, and developing tooth buds. Interestingly, Gasp1-/- ;Gdf11-/- mice had abnormal formation of lower incisors: tooth buds for lower incisors were under-developed or missing. Although Gdf11+/- mice were viable and had mild transformations of the axial skeleton, no specific defects in the craniofacial development have been observed in Gdf11+/- mice. However, loss of Gasp1 in Gdf11+/- mice occasionally resulted in small and abnormally shaped auricles. CONCLUSIONS: These findings suggest that both GASP-1 and GDF-11 play important roles in dental and craniofacial development both during embryogenesis and in adult tissues.
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