Skeletal Deficits in Male and Female down Syndrome Model Mice Arise Independent of Normalized Dyrk1a Expression in Osteoblasts
Trisomy 21 (Ts21) causes alterations in skeletal development resulting in decreased bone mass, shortened stature and weaker bones in individuals with Down syndrome (DS). There is a sexual dimorphism in bone mineral density (BMD) deficits associated with DS with males displaying earlier deficits than...
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MDPI AG
2021-10-01
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| Series: | Genes |
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| Online Access: | https://www.mdpi.com/2073-4425/12/11/1729 |
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| author | Jared R. Thomas Kourtney Sloan Kelsey Cave Joseph M. Wallace Randall J. Roper |
| author_facet | Jared R. Thomas Kourtney Sloan Kelsey Cave Joseph M. Wallace Randall J. Roper |
| author_sort | Jared R. Thomas |
| collection | DOAJ |
| description | Trisomy 21 (Ts21) causes alterations in skeletal development resulting in decreased bone mass, shortened stature and weaker bones in individuals with Down syndrome (DS). There is a sexual dimorphism in bone mineral density (BMD) deficits associated with DS with males displaying earlier deficits than females. The relationships between causative trisomic genes, cellular mechanisms, and influence of sex in DS skeletal abnormalities remain unknown. One hypothesis is that the low bone turnover phenotype observed in DS results from attenuated osteoblast function, contributing to impaired trabecular architecture, altered cortical geometry, and decreased mineralization. <i>DYRK1A</i>, found in three copies in humans with DS, Ts65Dn, and Dp1Tyb DS model mice, has been implicated in the development of postnatal skeletal phenotypes associated with DS. Reduced copy number of <i>Dyrk1a</i> to euploid levels from conception in an otherwise trisomic Ts65Dn mice resulted in a rescue of appendicular bone deficits, suggesting DYRK1A contributes to skeletal development and homeostasis. We hypothesized that reduction of <i>Dyrk1a</i> copy number in trisomic osteoblasts would improve cellular function and resultant skeletal structural anomalies in trisomic mice. Female mice with a floxed <i>Dyrk1a</i> gene (Ts65Dn,<i>Dyrk1a</i><sup>fl/wt</sup>) were mated with male <i>Osx-Cre<sup>+</sup></i> (expressed in osteoblasts beginning around E13.5) mice, resulting in reduced <i>Dyrk1a</i> copy number in mature osteoblasts in Ts65Dn,<i>Dyrk1a</i><sup>+/+/<i>Osx-Cre</i></sup> P42 male and female trisomic and euploid mice, compared with littermate controls. Male and female Ts65Dn,<i>Dyrk1a</i><sup>+/+/+</sup> (3 copies of DYRK1A in osteoblasts) and Ts65Dn,<i>Dyrk1a</i><sup>+/+/<i>Osx-Cre</i></sup> (2 copies of <i>Dyrk1a</i> in osteoblasts) displayed similar defects in both trabecular architecture and cortical geometry, with no improvements with reduced <i>Dyrk1a</i> in osteoblasts. This suggests that trisomic DYRK1A does not affect osteoblast function in a cell-autonomous manner at or before P42. Although male Dp1Tyb and Ts65Dn mice exhibit similar skeletal deficits at P42 in both trabecular and cortical bone compartments between euploid and trisomic mice, female Ts65Dn mice exhibit significant cortical and trabecular deficits at P42, in contrast to an absence of genotype effect in female Dp1Tyb mice in trabecular bone. Taken together, these data suggest skeletal deficits in DS mouse models and are sex and age dependent, and influenced by strain effects, but are not solely caused by the overexpression of <i>Dyrk1a</i> in osteoblasts. Identifying molecular and cellular mechanisms, disrupted by gene dosage imbalance, that are involved in the development of skeletal phenotypes associated with DS could help to design therapies to rescue skeletal deficiencies seen in DS. |
| first_indexed | 2024-03-10T05:28:38Z |
| format | Article |
| id | doaj.art-812ce9a77ca94c54b2844ed968d62d18 |
| institution | Directory Open Access Journal |
| issn | 2073-4425 |
| language | English |
| last_indexed | 2024-03-10T05:28:38Z |
| publishDate | 2021-10-01 |
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| record_format | Article |
| series | Genes |
| spelling | doaj.art-812ce9a77ca94c54b2844ed968d62d182023-11-22T23:27:56ZengMDPI AGGenes2073-44252021-10-011211172910.3390/genes12111729Skeletal Deficits in Male and Female down Syndrome Model Mice Arise Independent of Normalized Dyrk1a Expression in OsteoblastsJared R. Thomas0Kourtney Sloan1Kelsey Cave2Joseph M. Wallace3Randall J. Roper4Department of Biology, Indiana University-Purdue University Indianapolis, Indianapolis, IN 46202, USADepartment of Biology, Indiana University-Purdue University Indianapolis, Indianapolis, IN 46202, USADepartment of Biology, Indiana University-Purdue University Indianapolis, Indianapolis, IN 46202, USADepartment of Biomedical Engineering, Indiana University-Purdue University Indianapolis, Indianapolis, IN 46202, USADepartment of Biology, Indiana University-Purdue University Indianapolis, Indianapolis, IN 46202, USATrisomy 21 (Ts21) causes alterations in skeletal development resulting in decreased bone mass, shortened stature and weaker bones in individuals with Down syndrome (DS). There is a sexual dimorphism in bone mineral density (BMD) deficits associated with DS with males displaying earlier deficits than females. The relationships between causative trisomic genes, cellular mechanisms, and influence of sex in DS skeletal abnormalities remain unknown. One hypothesis is that the low bone turnover phenotype observed in DS results from attenuated osteoblast function, contributing to impaired trabecular architecture, altered cortical geometry, and decreased mineralization. <i>DYRK1A</i>, found in three copies in humans with DS, Ts65Dn, and Dp1Tyb DS model mice, has been implicated in the development of postnatal skeletal phenotypes associated with DS. Reduced copy number of <i>Dyrk1a</i> to euploid levels from conception in an otherwise trisomic Ts65Dn mice resulted in a rescue of appendicular bone deficits, suggesting DYRK1A contributes to skeletal development and homeostasis. We hypothesized that reduction of <i>Dyrk1a</i> copy number in trisomic osteoblasts would improve cellular function and resultant skeletal structural anomalies in trisomic mice. Female mice with a floxed <i>Dyrk1a</i> gene (Ts65Dn,<i>Dyrk1a</i><sup>fl/wt</sup>) were mated with male <i>Osx-Cre<sup>+</sup></i> (expressed in osteoblasts beginning around E13.5) mice, resulting in reduced <i>Dyrk1a</i> copy number in mature osteoblasts in Ts65Dn,<i>Dyrk1a</i><sup>+/+/<i>Osx-Cre</i></sup> P42 male and female trisomic and euploid mice, compared with littermate controls. Male and female Ts65Dn,<i>Dyrk1a</i><sup>+/+/+</sup> (3 copies of DYRK1A in osteoblasts) and Ts65Dn,<i>Dyrk1a</i><sup>+/+/<i>Osx-Cre</i></sup> (2 copies of <i>Dyrk1a</i> in osteoblasts) displayed similar defects in both trabecular architecture and cortical geometry, with no improvements with reduced <i>Dyrk1a</i> in osteoblasts. This suggests that trisomic DYRK1A does not affect osteoblast function in a cell-autonomous manner at or before P42. Although male Dp1Tyb and Ts65Dn mice exhibit similar skeletal deficits at P42 in both trabecular and cortical bone compartments between euploid and trisomic mice, female Ts65Dn mice exhibit significant cortical and trabecular deficits at P42, in contrast to an absence of genotype effect in female Dp1Tyb mice in trabecular bone. Taken together, these data suggest skeletal deficits in DS mouse models and are sex and age dependent, and influenced by strain effects, but are not solely caused by the overexpression of <i>Dyrk1a</i> in osteoblasts. Identifying molecular and cellular mechanisms, disrupted by gene dosage imbalance, that are involved in the development of skeletal phenotypes associated with DS could help to design therapies to rescue skeletal deficiencies seen in DS.https://www.mdpi.com/2073-4425/12/11/1729DYRK1ADown syndromeosteoblastssexual dimorphismgene dosageskeletal abnormalities |
| spellingShingle | Jared R. Thomas Kourtney Sloan Kelsey Cave Joseph M. Wallace Randall J. Roper Skeletal Deficits in Male and Female down Syndrome Model Mice Arise Independent of Normalized Dyrk1a Expression in Osteoblasts Genes DYRK1A Down syndrome osteoblasts sexual dimorphism gene dosage skeletal abnormalities |
| title | Skeletal Deficits in Male and Female down Syndrome Model Mice Arise Independent of Normalized Dyrk1a Expression in Osteoblasts |
| title_full | Skeletal Deficits in Male and Female down Syndrome Model Mice Arise Independent of Normalized Dyrk1a Expression in Osteoblasts |
| title_fullStr | Skeletal Deficits in Male and Female down Syndrome Model Mice Arise Independent of Normalized Dyrk1a Expression in Osteoblasts |
| title_full_unstemmed | Skeletal Deficits in Male and Female down Syndrome Model Mice Arise Independent of Normalized Dyrk1a Expression in Osteoblasts |
| title_short | Skeletal Deficits in Male and Female down Syndrome Model Mice Arise Independent of Normalized Dyrk1a Expression in Osteoblasts |
| title_sort | skeletal deficits in male and female down syndrome model mice arise independent of normalized dyrk1a expression in osteoblasts |
| topic | DYRK1A Down syndrome osteoblasts sexual dimorphism gene dosage skeletal abnormalities |
| url | https://www.mdpi.com/2073-4425/12/11/1729 |
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