New Insights into ADAMTS Metalloproteases in the Central Nervous System. 2020

Yamina Mohamedi, and Tania Fontanil, and Teresa Cobo, and Santiago Cal, and Alvaro J Obaya
Departamento de Bioquímica y Biología Molecular, Universidad de Oviedo, 33006 Oviedo, Asturias, Spain.

Components of the extracellular matrix (ECM) are key players in regulating cellular functions throughout the whole organism. In fact, ECM components not only participate in tissue organization but also contribute to processes such as cellular maintenance, proliferation, and migration, as well as to support for various signaling pathways. In the central nervous system (CNS), proteoglycans of the lectican family, such as versican, aggrecan, brevican, and neurocan, are important constituents of the ECM. In recent years, members of this family have been found to be involved in the maintenance of CNS homeostasis and to participate directly in processes such as the organization of perineural nets, the regulation of brain plasticity, CNS development, brain injury repair, axonal guidance, and even the altering of synaptic responses. ADAMTSs are a family of "A disintegrin and metalloproteinase with thrombospondin motifs" proteins that have been found to be involved in a multitude of processes through the degradation of lecticans and other proteoglycans. Recently, alterations in ADAMTS expression and activity have been found to be involved in neuronal disorders such as stroke, neurodegeneration, schizophrenia, and even Alzheimer's disease, which in turn may suggest their potential use as therapeutic targets. Herein, we summarize the different roles of ADAMTSs in regulating CNS events through interactions and the degradation of ECM components (more specifically, the lectican family of proteoglycans).

UI MeSH Term Description Entries
D011509 Proteoglycans Glycoproteins which have a very high polysaccharide content. Proteoglycan,Proteoglycan Type H
D001921 Brain The part of CENTRAL NERVOUS SYSTEM that is contained within the skull (CRANIUM). Arising from the NEURAL TUBE, the embryonic brain is comprised of three major parts including PROSENCEPHALON (the forebrain); MESENCEPHALON (the midbrain); and RHOMBENCEPHALON (the hindbrain). The developed brain consists of CEREBRUM; CEREBELLUM; and other structures in the BRAIN STEM. Encephalon
D001927 Brain Diseases Pathologic conditions affecting the BRAIN, which is composed of the intracranial components of the CENTRAL NERVOUS SYSTEM. This includes (but is not limited to) the CEREBRAL CORTEX; intracranial white matter; BASAL GANGLIA; THALAMUS; HYPOTHALAMUS; BRAIN STEM; and CEREBELLUM. Intracranial Central Nervous System Disorders,Brain Disorders,CNS Disorders, Intracranial,Central Nervous System Disorders, Intracranial,Central Nervous System Intracranial Disorders,Encephalon Diseases,Encephalopathy,Intracranial CNS Disorders,Brain Disease,Brain Disorder,CNS Disorder, Intracranial,Encephalon Disease,Encephalopathies,Intracranial CNS Disorder
D005109 Extracellular Matrix A meshwork-like substance found within the extracellular space and in association with the basement membrane of the cell surface. It promotes cellular proliferation and provides a supporting structure to which cells or cell lysates in culture dishes adhere. Matrix, Extracellular,Extracellular Matrices,Matrices, Extracellular
D006801 Humans Members of the species Homo sapiens. Homo sapiens,Man (Taxonomy),Human,Man, Modern,Modern Man
D000071096 ADAMTS Proteins A subfamily of ADAM proteases that are distinguished by the presence of one or more THROMBOSPONDIN type-1 repeats (TSRs). These are three-strand motifs that contain characteristic TRYPTOPHAN, ARGININE, and CYSTEINE residues respectively. In contrast to ADAM proteins, which reside on CELL MEMBRANES, ADAMTS proteases are secreted and function in the EXTRACELLULAR MATRIX. A Disintegrin And Metalloproteinase With Thrombospondin Motifs Protein,ADAMTS Protease,ADAMTS Protein,ADAMTS-Like Protein,ADAMTSL Protein,Adam Metallopeptidases With Thrombospondin Type 1 Motif Protein,A Disintegrin And Metalloproteinase With Thrombospondin Motifs Proteins,ADAMTS Proteases,ADAMTS-Like Proteins,ADAMTSL Proteins,Adam Metallopeptidases With Thrombospondin Type 1 Motif Proteins,ADAMTS Like Protein,ADAMTS Like Proteins,Protease, ADAMTS,Protein, ADAMTS,Protein, ADAMTS-Like,Protein, ADAMTSL
D000818 Animals Unicellular or multicellular, heterotrophic organisms, that have sensation and the power of voluntary movement. Under the older five kingdom paradigm, Animalia was one of the kingdoms. Under the modern three domain model, Animalia represents one of the many groups in the domain EUKARYOTA. Animal,Metazoa,Animalia
D001369 Axons Nerve fibers that are capable of rapidly conducting impulses away from the neuron cell body. Axon

Related Publications

Yamina Mohamedi, and Tania Fontanil, and Teresa Cobo, and Santiago Cal, and Alvaro J Obaya
March 1993, Neurochemistry international,
Yamina Mohamedi, and Tania Fontanil, and Teresa Cobo, and Santiago Cal, and Alvaro J Obaya
May 1999, Inflammation research : official journal of the European Histamine Research Society ... [et al.],
Yamina Mohamedi, and Tania Fontanil, and Teresa Cobo, and Santiago Cal, and Alvaro J Obaya
May 2007, Current rheumatology reports,
Yamina Mohamedi, and Tania Fontanil, and Teresa Cobo, and Santiago Cal, and Alvaro J Obaya
September 2017, Journal of neuroscience research,
Yamina Mohamedi, and Tania Fontanil, and Teresa Cobo, and Santiago Cal, and Alvaro J Obaya
August 1992, Rheumatic diseases clinics of North America,
Yamina Mohamedi, and Tania Fontanil, and Teresa Cobo, and Santiago Cal, and Alvaro J Obaya
July 2023, The international journal of neuropsychopharmacology,
Yamina Mohamedi, and Tania Fontanil, and Teresa Cobo, and Santiago Cal, and Alvaro J Obaya
November 2014, Current opinion in HIV and AIDS,
Yamina Mohamedi, and Tania Fontanil, and Teresa Cobo, and Santiago Cal, and Alvaro J Obaya
January 1990, Research publications - Association for Research in Nervous and Mental Disease,
Yamina Mohamedi, and Tania Fontanil, and Teresa Cobo, and Santiago Cal, and Alvaro J Obaya
April 2009, Nihon rinsho. Japanese journal of clinical medicine,
Yamina Mohamedi, and Tania Fontanil, and Teresa Cobo, and Santiago Cal, and Alvaro J Obaya
October 2013, Journal of neuroinflammation,
Copied contents to your clipboard!