Cargando…
Extracellular domain of CD98hc is required for early murine development
BACKGROUND: The multifunctional protein CD98 heavy chain (CD98hc, Slc3a2) associates with integrin β1 through its cytoplasmic and transmembrane domains and the CD98hc-mediated integrin signaling is required for maintenance of ES cell proliferation. CD98hc-null mice exhibit early post-implantation le...
Autores principales: | , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2011
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3125211/ https://www.ncbi.nlm.nih.gov/pubmed/21711689 http://dx.doi.org/10.1186/2045-3701-1-7 |
_version_ | 1782207181356007424 |
---|---|
author | Sato, Yukiyasu Heimeier, Rachel A Li, Cuiling Deng, Chuxia Shi, Yun-Bo |
author_facet | Sato, Yukiyasu Heimeier, Rachel A Li, Cuiling Deng, Chuxia Shi, Yun-Bo |
author_sort | Sato, Yukiyasu |
collection | PubMed |
description | BACKGROUND: The multifunctional protein CD98 heavy chain (CD98hc, Slc3a2) associates with integrin β1 through its cytoplasmic and transmembrane domains and the CD98hc-mediated integrin signaling is required for maintenance of ES cell proliferation. CD98hc-null mice exhibit early post-implantation lethality similar to integrin β1-null mice, supporting the importance of its interaction with integrin β1. On the other hand, the extracellular domain of CD98hc interacts with L-type amino acid transporters (LATs) and is essential for appropriate cell surface distribution of LATs. LATs mediate the transport of amino acids and other molecules such as thyroid hormone. In this respect, CD98hc may also affect development via these transporters. RESULTS: In this study, mice were generated from embryonic stem (ES) cell line (PST080) harboring a mutant CD98hc allele (CD98hc(Δ/+)). Expression of the CD98hc mutant allele results in ΔCD98hc-β geo fusion protein where extracellular C-terminal 102 amino acids of CD98hc are replaced with β geo. Analyses of PST080 ES cells as well as reconstituted frog oocytes demonstrated that ΔCD98hc-β geo fusion protein preserved its ability to interact with integrin β1 although this mutant protein was hardly localized on the cell surface. These findings suggest that ΔCD98hc-β geo protein can mediate integrin signaling but cannot support amino acid transport through LATs. CD98hc(Δ/+ )mice were normal. Although some of the implantation sites lacked embryonic component at E9.5, all the implantation sites contained embryonic component at E7.5. Thus, CD98hc(Δ/Δ )embryos are likely to die between E7.5 and E9.5. CONCLUSIONS: Considering that CD98hc complete knockout (CD98hc(-/-)) embryos are reported to die shortly after implantation, our findings suggest potential stage-specific roles of CD98hc in murine embryonic development. CD98hc may be essential for early post-implantation development by regulating integrin-dependent signaling, while the other function of CD98hc as a component of amino acid transporters may be required for embryonic development at later stages. |
format | Online Article Text |
id | pubmed-3125211 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-31252112011-06-29 Extracellular domain of CD98hc is required for early murine development Sato, Yukiyasu Heimeier, Rachel A Li, Cuiling Deng, Chuxia Shi, Yun-Bo Cell Biosci Research BACKGROUND: The multifunctional protein CD98 heavy chain (CD98hc, Slc3a2) associates with integrin β1 through its cytoplasmic and transmembrane domains and the CD98hc-mediated integrin signaling is required for maintenance of ES cell proliferation. CD98hc-null mice exhibit early post-implantation lethality similar to integrin β1-null mice, supporting the importance of its interaction with integrin β1. On the other hand, the extracellular domain of CD98hc interacts with L-type amino acid transporters (LATs) and is essential for appropriate cell surface distribution of LATs. LATs mediate the transport of amino acids and other molecules such as thyroid hormone. In this respect, CD98hc may also affect development via these transporters. RESULTS: In this study, mice were generated from embryonic stem (ES) cell line (PST080) harboring a mutant CD98hc allele (CD98hc(Δ/+)). Expression of the CD98hc mutant allele results in ΔCD98hc-β geo fusion protein where extracellular C-terminal 102 amino acids of CD98hc are replaced with β geo. Analyses of PST080 ES cells as well as reconstituted frog oocytes demonstrated that ΔCD98hc-β geo fusion protein preserved its ability to interact with integrin β1 although this mutant protein was hardly localized on the cell surface. These findings suggest that ΔCD98hc-β geo protein can mediate integrin signaling but cannot support amino acid transport through LATs. CD98hc(Δ/+ )mice were normal. Although some of the implantation sites lacked embryonic component at E9.5, all the implantation sites contained embryonic component at E7.5. Thus, CD98hc(Δ/Δ )embryos are likely to die between E7.5 and E9.5. CONCLUSIONS: Considering that CD98hc complete knockout (CD98hc(-/-)) embryos are reported to die shortly after implantation, our findings suggest potential stage-specific roles of CD98hc in murine embryonic development. CD98hc may be essential for early post-implantation development by regulating integrin-dependent signaling, while the other function of CD98hc as a component of amino acid transporters may be required for embryonic development at later stages. BioMed Central 2011-02-25 /pmc/articles/PMC3125211/ /pubmed/21711689 http://dx.doi.org/10.1186/2045-3701-1-7 Text en Copyright ©2011 Sato et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Sato, Yukiyasu Heimeier, Rachel A Li, Cuiling Deng, Chuxia Shi, Yun-Bo Extracellular domain of CD98hc is required for early murine development |
title | Extracellular domain of CD98hc is required for early murine development |
title_full | Extracellular domain of CD98hc is required for early murine development |
title_fullStr | Extracellular domain of CD98hc is required for early murine development |
title_full_unstemmed | Extracellular domain of CD98hc is required for early murine development |
title_short | Extracellular domain of CD98hc is required for early murine development |
title_sort | extracellular domain of cd98hc is required for early murine development |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3125211/ https://www.ncbi.nlm.nih.gov/pubmed/21711689 http://dx.doi.org/10.1186/2045-3701-1-7 |
work_keys_str_mv | AT satoyukiyasu extracellulardomainofcd98hcisrequiredforearlymurinedevelopment AT heimeierrachela extracellulardomainofcd98hcisrequiredforearlymurinedevelopment AT licuiling extracellulardomainofcd98hcisrequiredforearlymurinedevelopment AT dengchuxia extracellulardomainofcd98hcisrequiredforearlymurinedevelopment AT shiyunbo extracellulardomainofcd98hcisrequiredforearlymurinedevelopment |