2018
DOI: 10.1161/jaha.117.008260
|View full text |Cite
|
Sign up to set email alerts
|

LRRC10 (Leucine‐Rich Repeat Containing Protein 10) and REEP5 (Receptor Accessory Protein 5) as Novel Regulators of Cardiac Excitation‐Contraction Coupling Structure and Function

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
4
1

Citation Types

0
6
0

Year Published

2020
2020
2024
2024

Publication Types

Select...
4
2
1

Relationship

0
7

Authors

Journals

citations
Cited by 8 publications
(6 citation statements)
references
References 22 publications
0
6
0
Order By: Relevance
“…31,32 Chiamvimonvat et al demonstrated that REEP5, as the only REEP family protein enriched in the heart, is a new regulator of cardiac excitation-contraction coupling. 33 Studies have also shown that the expression of REEP5 is down-regulated in lung and gastric cancer. 34,35 REEP5 knockdown affected CXCR1 and down-regulated the IL-8-mediated cellular response, which significantly reduced the growth and invasion of lung cancer cells.…”
Section: Discussionmentioning
confidence: 99%
“…31,32 Chiamvimonvat et al demonstrated that REEP5, as the only REEP family protein enriched in the heart, is a new regulator of cardiac excitation-contraction coupling. 33 Studies have also shown that the expression of REEP5 is down-regulated in lung and gastric cancer. 34,35 REEP5 knockdown affected CXCR1 and down-regulated the IL-8-mediated cellular response, which significantly reduced the growth and invasion of lung cancer cells.…”
Section: Discussionmentioning
confidence: 99%
“…REEPs are a group of receptor expression-enhancing proteins that can help the proper functional expression of G-protein-coupled receptors ( Park et al, 2016 ; Chiamvimonvat and Song, 2018 ). The REEP 5 gene, also known as DP1, is one of the DP1/Yop1p protein family members that engage in endoplasmic reticulum tubule formation ( Yang et al, 2012 ).…”
Section: Discussionmentioning
confidence: 99%
“…REEP5 is a novel regulator of cardiac excitation‐contraction by shaping the morphology of the junctional sarcoplasmic reticulum ( SR ), whereas REEP5 deficiency led to a defect in the SR and T‐tubules connections ( Yao et al, 2018 ). Meanwhile, downregulation of REEP5 was observed in a heart failure model induced by chronic pressure, suggesting the potential role of REEP5 in cardiac dysfunction ( Chiamvimonvat and Song, 2018 ). In addition, REEP5 is associated with neuropsychiatric and retinal disorders and hereditary spastic paraplegia ( Park, et al, 2016 ; Chiamvimonvat and Song, 2018 ).…”
Section: Discussionmentioning
confidence: 99%
See 1 more Smart Citation
“…Despite the fact that 28 genes are a low input for a gene ontology analysis, the categories found are closely related to the phenotypes described upon Meis loss of function, which suggests this gene list is relevant to the mechanisms involved in the phenotypic alterations. Furthermore, Fhl2 and Lrrc10, which are strongly downregulated, have been previously as hypertrophic growth repressor (Okamoto et al, 2013) and cardiac excitation-contraction coupling regulator, respectively (Chiamvimonvat & Song, 2018). By contrast, nothing has been reported before about EfnB3 expression or function in the heart, despite of being one of the most downregulated in Meis mutants.…”
Section: Putative Direct Targets Of Meismentioning
confidence: 97%