Cargando…
ADAMTS-12: Functions and Challenges for a Complex Metalloprotease
Nineteen members of the ADAMTS family of secreted zinc metalloproteinases are present in the human degradome. A wide range of different functions are being attributed to these enzymes and the number of their known substrates is considerably increasing in recent years. ADAMTSs can participate in proc...
Autores principales: | , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2021
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8119882/ https://www.ncbi.nlm.nih.gov/pubmed/33996918 http://dx.doi.org/10.3389/fmolb.2021.686763 |
_version_ | 1783691948466372608 |
---|---|
author | Mohamedi, Yamina Fontanil, Tania Cal, Santiago Cobo, Teresa Obaya, Álvaro J. |
author_facet | Mohamedi, Yamina Fontanil, Tania Cal, Santiago Cobo, Teresa Obaya, Álvaro J. |
author_sort | Mohamedi, Yamina |
collection | PubMed |
description | Nineteen members of the ADAMTS family of secreted zinc metalloproteinases are present in the human degradome. A wide range of different functions are being attributed to these enzymes and the number of their known substrates is considerably increasing in recent years. ADAMTSs can participate in processes such as fertility, inflammation, arthritis, neuronal and behavioral disorders, as well as cancer. Since its first annotation in 2001, ADAMTS-12 has been described to participate in different processes displayed by members of this family of proteinases. In this sense, ADAMTS-12 performs essential roles in modulation and recovery from inflammatory processes such as colitis, endotoxic sepsis and pancreatitis. ADAMTS-12 has also been involved in cancer development acting either as a tumor suppressor or as a pro-tumoral agent. Furthermore, participation of ADAMTS-12 in arthritis or in neuronal disorders has also been suggested through degradation of components of the extracellular matrix. In addition, ADAMTS-12 proteinase activity can also be modified by interaction with other proteins and thus, can be an alternative way of modulating ADAMTS-12 functions. In this review we revised the most relevant findings about ADAMTS-12 function on the 20th anniversary of its identification. |
format | Online Article Text |
id | pubmed-8119882 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-81198822021-05-15 ADAMTS-12: Functions and Challenges for a Complex Metalloprotease Mohamedi, Yamina Fontanil, Tania Cal, Santiago Cobo, Teresa Obaya, Álvaro J. Front Mol Biosci Molecular Biosciences Nineteen members of the ADAMTS family of secreted zinc metalloproteinases are present in the human degradome. A wide range of different functions are being attributed to these enzymes and the number of their known substrates is considerably increasing in recent years. ADAMTSs can participate in processes such as fertility, inflammation, arthritis, neuronal and behavioral disorders, as well as cancer. Since its first annotation in 2001, ADAMTS-12 has been described to participate in different processes displayed by members of this family of proteinases. In this sense, ADAMTS-12 performs essential roles in modulation and recovery from inflammatory processes such as colitis, endotoxic sepsis and pancreatitis. ADAMTS-12 has also been involved in cancer development acting either as a tumor suppressor or as a pro-tumoral agent. Furthermore, participation of ADAMTS-12 in arthritis or in neuronal disorders has also been suggested through degradation of components of the extracellular matrix. In addition, ADAMTS-12 proteinase activity can also be modified by interaction with other proteins and thus, can be an alternative way of modulating ADAMTS-12 functions. In this review we revised the most relevant findings about ADAMTS-12 function on the 20th anniversary of its identification. Frontiers Media S.A. 2021-04-30 /pmc/articles/PMC8119882/ /pubmed/33996918 http://dx.doi.org/10.3389/fmolb.2021.686763 Text en Copyright © 2021 Mohamedi, Fontanil, Cal, Cobo and Obaya. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Molecular Biosciences Mohamedi, Yamina Fontanil, Tania Cal, Santiago Cobo, Teresa Obaya, Álvaro J. ADAMTS-12: Functions and Challenges for a Complex Metalloprotease |
title | ADAMTS-12: Functions and Challenges for a Complex Metalloprotease |
title_full | ADAMTS-12: Functions and Challenges for a Complex Metalloprotease |
title_fullStr | ADAMTS-12: Functions and Challenges for a Complex Metalloprotease |
title_full_unstemmed | ADAMTS-12: Functions and Challenges for a Complex Metalloprotease |
title_short | ADAMTS-12: Functions and Challenges for a Complex Metalloprotease |
title_sort | adamts-12: functions and challenges for a complex metalloprotease |
topic | Molecular Biosciences |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8119882/ https://www.ncbi.nlm.nih.gov/pubmed/33996918 http://dx.doi.org/10.3389/fmolb.2021.686763 |
work_keys_str_mv | AT mohamediyamina adamts12functionsandchallengesforacomplexmetalloprotease AT fontaniltania adamts12functionsandchallengesforacomplexmetalloprotease AT calsantiago adamts12functionsandchallengesforacomplexmetalloprotease AT coboteresa adamts12functionsandchallengesforacomplexmetalloprotease AT obayaalvaroj adamts12functionsandchallengesforacomplexmetalloprotease |