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Why do humans need thrombospondin-1?
Matricellular proteins comprise several families of secreted proteins that function in higher animals at the interface between cells and their surrounding extracellular matrix. Targeted gene disruptions that result in loss of viability in mice have revealed critical roles for several matricellular p...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Springer Netherlands
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10409698/ https://www.ncbi.nlm.nih.gov/pubmed/36689135 http://dx.doi.org/10.1007/s12079-023-00722-5 |
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author | Kaur, Sukhbir Roberts, David D. |
author_facet | Kaur, Sukhbir Roberts, David D. |
author_sort | Kaur, Sukhbir |
collection | PubMed |
description | Matricellular proteins comprise several families of secreted proteins that function in higher animals at the interface between cells and their surrounding extracellular matrix. Targeted gene disruptions that result in loss of viability in mice have revealed critical roles for several matricellular proteins in murine embryonic development, including two members of the cellular communication network (CCN) gene family. In contrast, mice lacking single or multiple members of the thrombospondin (THBS) gene family remain viable and fertile. The frequency of loss of function mutants, identified using human deep exome sequencing data, provided evidence that some of the essential genes in mice, including Ccn1, are also essential genes in humans. However, a deficit in loss of function mutants in humans indicated that THBS1 is also highly loss-intolerant. In addition to roles in embryonic development or adult reproduction, genes may be loss-intolerant in humans because their function is needed to survive environmental stresses that are encountered between birth and reproduction. Laboratory mice live in a protected environment that lacks the exposures to pathogens and injury that humans routinely face. However, subjecting Thbs1(−/−) mice to defined stresses has provided valuable insights into functions of thrombospondin-1 that could account for the loss-intolerance of THBS1 in humans. GRAPHICAL ABSTRACT: [Figure: see text] |
format | Online Article Text |
id | pubmed-10409698 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Springer Netherlands |
record_format | MEDLINE/PubMed |
spelling | pubmed-104096982023-08-10 Why do humans need thrombospondin-1? Kaur, Sukhbir Roberts, David D. J Cell Commun Signal Review Matricellular proteins comprise several families of secreted proteins that function in higher animals at the interface between cells and their surrounding extracellular matrix. Targeted gene disruptions that result in loss of viability in mice have revealed critical roles for several matricellular proteins in murine embryonic development, including two members of the cellular communication network (CCN) gene family. In contrast, mice lacking single or multiple members of the thrombospondin (THBS) gene family remain viable and fertile. The frequency of loss of function mutants, identified using human deep exome sequencing data, provided evidence that some of the essential genes in mice, including Ccn1, are also essential genes in humans. However, a deficit in loss of function mutants in humans indicated that THBS1 is also highly loss-intolerant. In addition to roles in embryonic development or adult reproduction, genes may be loss-intolerant in humans because their function is needed to survive environmental stresses that are encountered between birth and reproduction. Laboratory mice live in a protected environment that lacks the exposures to pathogens and injury that humans routinely face. However, subjecting Thbs1(−/−) mice to defined stresses has provided valuable insights into functions of thrombospondin-1 that could account for the loss-intolerance of THBS1 in humans. GRAPHICAL ABSTRACT: [Figure: see text] Springer Netherlands 2023-01-23 2023-09 /pmc/articles/PMC10409698/ /pubmed/36689135 http://dx.doi.org/10.1007/s12079-023-00722-5 Text en © This is a U.S. Government work and not under copyright protection in the US; foreign copyright protection may apply 2023 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Review Kaur, Sukhbir Roberts, David D. Why do humans need thrombospondin-1? |
title | Why do humans need thrombospondin-1? |
title_full | Why do humans need thrombospondin-1? |
title_fullStr | Why do humans need thrombospondin-1? |
title_full_unstemmed | Why do humans need thrombospondin-1? |
title_short | Why do humans need thrombospondin-1? |
title_sort | why do humans need thrombospondin-1? |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10409698/ https://www.ncbi.nlm.nih.gov/pubmed/36689135 http://dx.doi.org/10.1007/s12079-023-00722-5 |
work_keys_str_mv | AT kaursukhbir whydohumansneedthrombospondin1 AT robertsdavidd whydohumansneedthrombospondin1 |