Activation of mTOR signaling in adult lung microvascular progenitor cells accelerates lung aging
Reactivation and dysregulation of the mTOR signaling pathway are a hallmark of aging and chronic lung disease; however, the impact on microvascular progenitor cells (MVPCs), capillary angiostasis, and tissue homeostasis is unknown. While the existence of an adult lung vascular progenitor has long been hypothesized, these studies show that Abcg2 enriches for a population of angiogenic tissue-resident MVPCs present in both adult mouse and human lungs using functional, lineage, and transcriptomic analyses. These studies link human and mouse MVPC-specific mTORC1 activation to decreased stemness, angiogenic potential, and disruption of p53 and Wnt pathways, with consequent loss of alveolar-capillary structure and function. Following mTOR activation, these MVPCs adapt a unique transcriptome signature and emerge as a venous subpopulation in the angiodiverse microvascular endothelial subclusters. Thus, our findings support a significant role for mTOR in the maintenance of MVPC function and microvascular niche homeostasis as well as a cell-based mechanism driving loss of tissue structure underlying lung aging and the development of emphysema.
Medienart: |
E-Artikel |
---|
Erscheinungsjahr: |
2023 |
---|---|
Erschienen: |
2023 |
Enthalten in: |
Zur Gesamtaufnahme - volume:133 |
---|---|
Enthalten in: |
The Journal of clinical investigation - 133(2023), 24 vom: 15. Dez. |
Sprache: |
Englisch |
---|
Beteiligte Personen: |
Mason, Emma C [VerfasserIn] |
---|
Links: |
---|
Themen: |
Adult stem cells |
---|
Anmerkungen: |
Date Completed 16.12.2023 Date Revised 16.12.2023 published: Electronic Citation Status MEDLINE |
---|
doi: |
10.1172/JCI171430 |
---|
funding: |
|
---|---|
Förderinstitution / Projekttitel: |
|
PPN (Katalog-ID): |
NLM363669205 |
---|
LEADER | 01000caa a22002652 4500 | ||
---|---|---|---|
001 | NLM363669205 | ||
003 | DE-627 | ||
005 | 20231227133115.0 | ||
007 | cr uuu---uuuuu | ||
008 | 231226s2023 xx |||||o 00| ||eng c | ||
024 | 7 | |a 10.1172/JCI171430 |2 doi | |
028 | 5 | 2 | |a pubmed24n1230.xml |
035 | |a (DE-627)NLM363669205 | ||
035 | |a (NLM)37874650 | ||
035 | |a (PII)e171430 | ||
040 | |a DE-627 |b ger |c DE-627 |e rakwb | ||
041 | |a eng | ||
100 | 1 | |a Mason, Emma C |e verfasserin |4 aut | |
245 | 1 | 0 | |a Activation of mTOR signaling in adult lung microvascular progenitor cells accelerates lung aging |
264 | 1 | |c 2023 | |
336 | |a Text |b txt |2 rdacontent | ||
337 | |a ƒaComputermedien |b c |2 rdamedia | ||
338 | |a ƒa Online-Ressource |b cr |2 rdacarrier | ||
500 | |a Date Completed 16.12.2023 | ||
500 | |a Date Revised 16.12.2023 | ||
500 | |a published: Electronic | ||
500 | |a Citation Status MEDLINE | ||
520 | |a Reactivation and dysregulation of the mTOR signaling pathway are a hallmark of aging and chronic lung disease; however, the impact on microvascular progenitor cells (MVPCs), capillary angiostasis, and tissue homeostasis is unknown. While the existence of an adult lung vascular progenitor has long been hypothesized, these studies show that Abcg2 enriches for a population of angiogenic tissue-resident MVPCs present in both adult mouse and human lungs using functional, lineage, and transcriptomic analyses. These studies link human and mouse MVPC-specific mTORC1 activation to decreased stemness, angiogenic potential, and disruption of p53 and Wnt pathways, with consequent loss of alveolar-capillary structure and function. Following mTOR activation, these MVPCs adapt a unique transcriptome signature and emerge as a venous subpopulation in the angiodiverse microvascular endothelial subclusters. Thus, our findings support a significant role for mTOR in the maintenance of MVPC function and microvascular niche homeostasis as well as a cell-based mechanism driving loss of tissue structure underlying lung aging and the development of emphysema | ||
650 | 4 | |a Journal Article | |
650 | 4 | |a Adult stem cells | |
650 | 4 | |a Endothelial cells | |
650 | 4 | |a Microcirculation | |
650 | 4 | |a Stem cells | |
650 | 4 | |a Vascular Biology | |
650 | 7 | |a TOR Serine-Threonine Kinases |2 NLM | |
650 | 7 | |a EC 2.7.11.1 |2 NLM | |
700 | 1 | |a Menon, Swapna |e verfasserin |4 aut | |
700 | 1 | |a Schneider, Benjamin R |e verfasserin |4 aut | |
700 | 1 | |a Gaskill, Christa F |e verfasserin |4 aut | |
700 | 1 | |a Dawson, Maggie M |e verfasserin |4 aut | |
700 | 1 | |a Moore, Camille M |e verfasserin |4 aut | |
700 | 1 | |a Armstrong, Laura Craig |e verfasserin |4 aut | |
700 | 1 | |a Cho, Okyong |e verfasserin |4 aut | |
700 | 1 | |a Richmond, Bradley W |e verfasserin |4 aut | |
700 | 1 | |a Kropski, Jonathan A |e verfasserin |4 aut | |
700 | 1 | |a West, James D |e verfasserin |4 aut | |
700 | 1 | |a Geraghty, Patrick |e verfasserin |4 aut | |
700 | 1 | |a Gomperts, Brigitte N |e verfasserin |4 aut | |
700 | 1 | |a Ess, Kevin C |e verfasserin |4 aut | |
700 | 1 | |a Gally, Fabienne |e verfasserin |4 aut | |
700 | 1 | |a Majka, Susan M |e verfasserin |4 aut | |
773 | 0 | 8 | |i Enthalten in |t The Journal of clinical investigation |d 1924 |g 133(2023), 24 vom: 15. Dez. |w (DE-627)NLM000005487 |x 1558-8238 |7 nnns |
773 | 1 | 8 | |g volume:133 |g year:2023 |g number:24 |g day:15 |g month:12 |
856 | 4 | 0 | |u http://dx.doi.org/10.1172/JCI171430 |3 Volltext |
912 | |a GBV_USEFLAG_A | ||
912 | |a GBV_NLM | ||
951 | |a AR | ||
952 | |d 133 |j 2023 |e 24 |b 15 |c 12 |