2019
DOI: 10.1007/s00018-019-03173-7
|View full text |Cite
|
Sign up to set email alerts
|

Functions of ‘A disintegrin and metalloproteases (ADAMs)’ in the mammalian nervous system

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
2
1
1

Citation Types

1
79
0

Year Published

2019
2019
2024
2024

Publication Types

Select...
7
2

Relationship

0
9

Authors

Journals

citations
Cited by 98 publications
(80 citation statements)
references
References 262 publications
1
79
0
Order By: Relevance
“…By the end of the lactation period (PPD 22) only a few perisomatic PNNs positive cells are still present with a surrounding interneuronal diffuse staining. These results suggest a complex PNNs degradation process probably involving the action of matrix metalloproteinases 66 , an underlying mechanism for a programmed PNNs degradation, or a passive mechanism of disassembly combined with transient synthesis events.…”
Section: The Pnns Expression In the Mpoa Persists After Parturition mentioning
confidence: 85%
“…By the end of the lactation period (PPD 22) only a few perisomatic PNNs positive cells are still present with a surrounding interneuronal diffuse staining. These results suggest a complex PNNs degradation process probably involving the action of matrix metalloproteinases 66 , an underlying mechanism for a programmed PNNs degradation, or a passive mechanism of disassembly combined with transient synthesis events.…”
Section: The Pnns Expression In the Mpoa Persists After Parturition mentioning
confidence: 85%
“…ADAM9, a type I transmembrane protein, is a catalytically active metalloprotease-disintegrin protein involved in multiple biological processes (Oria et al, 2018;Hsia et al, 2019). Specifically, ADAM9 acts as an α-secretase to cleave APP in nonamyloidogenic pathway producing sAPPα (Koike et al, 1999).…”
Section: Discussionmentioning
confidence: 99%
“…However, further experiments have to include various substrates of ADAM10 and ADAM17 to avoid many deleterious consequences by activating these enzymes. Moreover, additional experiments are needed to clearly show that the major target of E144 is ADAM17 over ADAM10 since it has been reported that ADAM17-mediated alpha cleavage of APP, referred to as the "regulated" pathway, is mostly occurring when PKC is stimulated [13,15,16]. Since activation of GPCR can increase APP processing by α-secretase via ADAM17 [13], the effect of E144 on ADAM17 may occur through GPCR signaling.…”
Section: Discussionmentioning
confidence: 99%
“…Among three family members, ADAM10 is considered as sheddase for APP and other diverse cell-surface proteins, including cytokines, cell adhesion molecules (CAMs), and Notch [13,14]. In contrast, ADAM9 and ADAM17 are believed to undertake regulated APP cleavage [13,15,16]. However, several studies demonstrated that ADAM9 could mimic the constitutive function of ADAM10 in microglia cells [17,18].…”
mentioning
confidence: 99%