Evidence map›Paper›PMID 35384838›Full record

ArticleeLife2022

Acquisition of cellular properties during alveolar formation requires differential activity and distribution of mitochondria.

Kuan Zhang, Erica Yao, Biao Chen, Ethan Chuang, Julia Wong, Robert I Seed, Stephen L Nishimura, Paul J Wolters, Pao-Tien Chuang

Open access · goldAbstract read
In one paragraph

Article in eLife, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
3.0field-weighted citation impact, top 8% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

19 citing papers in PubMed, 21 citations in OpenAlex.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

9 authors.

Kuan ZhangCardiovascular Research Institute, University of California, San Francisco, United States.ORCID 0000-0002-9723-1328
Erica YaoCardiovascular Research Institute, University of California, San Francisco, United States.
Biao ChenCardiovascular Research Institute, University of California, San Francisco, United States.
Ethan ChuangCardiovascular Research Institute, University of California, San Francisco, United States.
Julia WongCardiovascular Research Institute, University of California, San Francisco, United States.
Robert I SeedDepartment of Pathology, University of California, San Francisco, United States.
Stephen L NishimuraDepartment of Pathology, University of California, San Francisco, United States.
Paul J WoltersDivision of Pulmonary, Critical Care, Allergy and Sleep Medicine, Department of Medicine, University of California, San Francisco, United States.
Pao-Tien ChuangCardiovascular Research Institute, University of California, San Francisco, United States.ORCID 0000-0002-8961-8653

Funding

Molecular mechanisms of alveolar development and regenerationR01HL142876 · NHLBI · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI CHUANG, PAO-TIEN · 2018 to 2021
$2.1M
NHLBI NIH HHS R01 HL142876
6 · The paper itself

Abstract

Alveolar formation requires coordinated movement and interaction between alveolar epithelial cells, mesenchymal myofibroblasts, and endothelial cells/pericytes to produce secondary septa. These processes rely on the acquisition of distinct cellular properties to enable ligand secretion for cell-cell signaling and initiate morphogenesis through cellular contraction, cell migration, and cell shape change. In this study, we showed that mitochondrial activity and distribution play a key role in bestowing cellular functions on both alveolar epithelial cells and mesenchymal myofibroblasts for generating secondary septa to form alveoli in mice. These results suggest that mitochondrial function is tightly regulated to empower cellular machineries in a spatially specific manner. Indeed, such regulation via mitochondria is required for secretion of ligands, such as platelet-derived growth factor, from alveolar epithelial cells to influence myofibroblast proliferation and contraction/migration. Moreover, mitochondrial function enables myofibroblast contraction/migration during alveolar formation. Together, these findings yield novel mechanistic insights into how mitochondria regulate pivotal steps of alveologenesis. They highlight selective utilization of energy in cells and diverse energy demands in different cellular processes during development. Our work serves as a paradigm for studying how mitochondria control tissue patterning.

Indexed as

Endothelial CellsPulmonary AlveoliAnimalsCell MovementLungMiceMitochondriaMyofibroblastsactivityalveolusdevelopmental biologydistributionlungmitochondriamouse

Identifiers

PMID35384838
PMCPMC9183236
OpenAlexW4226186162

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.