2022
DOI: 10.1038/s41467-021-27860-x
|View full text |Cite
|
Sign up to set email alerts
|

Lung emphysema and impaired macrophage elastase clearance in mucolipin 3 deficient mice

Abstract: Lung emphysema and chronic bronchitis are the two most common causes of chronic obstructive pulmonary disease. Excess macrophage elastase MMP-12, which is predominantly secreted from alveolar macrophages, is known to mediate the development of lung injury and emphysema. Here, we discovered the endolysosomal cation channel mucolipin 3 (TRPML3) as a regulator of MMP-12 reuptake from broncho-alveolar fluid, driving in two independently generated Trpml3−/− mouse models enlarged lung injury, which is further exacer… Show more

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
1
1
1
1

Citation Types

0
17
0

Year Published

2022
2022
2024
2024

Publication Types

Select...
5
3

Relationship

2
6

Authors

Journals

citations
Cited by 31 publications
(17 citation statements)
references
References 75 publications
0
17
0
Order By: Relevance
“…Therefore, activation of TRPV2 channels may protect from cigarette smoke-induced COPD in alveoli. A similar mechanism was observed in TRPML3-deficient mice, which showed emphysema-like changes that were further exacerbated by exposure to tobacco smoke [ 127 ]. These changes were linked to an impaired early endolysosomal trafficking as well as defects in endocytosis in TRPML3−/− mice [ 127 ].…”
Section: Trp Expression and Function In Alveolimentioning
confidence: 52%
“…Therefore, activation of TRPV2 channels may protect from cigarette smoke-induced COPD in alveoli. A similar mechanism was observed in TRPML3-deficient mice, which showed emphysema-like changes that were further exacerbated by exposure to tobacco smoke [ 127 ]. These changes were linked to an impaired early endolysosomal trafficking as well as defects in endocytosis in TRPML3−/− mice [ 127 ].…”
Section: Trp Expression and Function In Alveolimentioning
confidence: 52%
“…However, these activators lack specificity for TRPML channel subtypes ( Grimm, 2016 ; Plesch et al, 2018 ; Shen et al, 2012 ). Recently, an isoform-selective activator for TRPML1, based on the structure of MLSA-1, called ML1-SA-1, has been developed by introduction of four additional chlorine substituents in the phthalimide subunit as characterized in Spix et al (2022) ( Fig. 1 A).…”
Section: Resultsmentioning
confidence: 99%
“…Only P2X4 and its role in surfactant release from lamellar bodies, lysosome-related organelles is well proven; likewise, the recent study of TRPML3 and its role for emphysema formation is strongly linked to its expression in endolysosomes. Plasma membrane expression of TRPML3 in endogenous cell systems including alveolar macrophages could not be confirmed [ 1 ]. By contrast, while the patch-clamp evidence for BK in endolysosomes is very convincing, potential roles in lung function seem not connected to endolysosomes.…”
Section: Discussionmentioning
confidence: 99%
“…Spix et al recently reported the first bona fide single TRPML3 knockout disease phenotype [ 1 ]. In two independently generated Trpml3 knockout mouse models, lung function measurements revealed an emphysema-like phenotype under basal conditions which strongly exacerbated under elastase treatment or tobacco smoke exposure.…”
Section: Trpml3—regulator Of Mmp-12 Levels In Bronchoalveolar Fluid: Early Endosomes Of Alveolar Macrophagesmentioning
confidence: 99%
See 1 more Smart Citation