Evidence map›Paper›PMID 42012134›Full record

ReviewPhysiological reviews2026

Transitional cell states at the crossroads of development, disease, and repair-regeneration.

Xiangyi Ke, Wellington V Cardoso

Abstract readReview
In one paragraph

Review in Physiological reviews, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

2 authors.

Xiangyi KeColumbia Center for Human Development, Department of Medicine, and Department of Genetics and Development, Columbia University Irving Medical Center, New York, New York, United States.
Wellington V CardosoColumbia Center for Human Development, Department of Medicine, and Department of Genetics and Development, Columbia University Irving Medical Center, New York, New York, United States.ORCID 0000-0002-8868-9716

Funding

T1alpha in type I cell formation, regulation &functionP01HL047049 · NHLBI · BOSTON UNIVERSITY MEDICAL CAMPUS · PI RAMIREZ, MARIA ISABEL · 1992 to 2012
$27.6M
Regulation of Progenitor Cell Plasticity in Lung Development and Disease-RepairR35HL166661 · NHLBI · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI Wellington V. Cardoso · 2023 to 2026
$4.4M
Local translation and viral infection in the airway epitheliumR01AI170904 · NIAID · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI Wellington V. Cardoso · 2023 to 2026
$2.6M
HHS | NIH | National Heart, Lung, and Blood Institute (NHLBI) R35 HL166661-01HHS | NIH | National Institute of Allergy and Infectious Diseases (NIAID) R01 AI170904-01NHLBI NIH HHS P01 HL047049NHLBI NIH HHS R35 HL166661NIAID NIH HHS R01 AI170904
6 · The paper itself

Abstract

Cells undergoing transitional states have been broadly referred to as plastic intermediates emerging between stable identities in multiple biological contexts. Once regarded as indistinct midpoints on lineage trajectories, these states are now recognized as discrete, biologically meaningful epigenetically permissive states, exquisitely responsive to environmental and stress signals at critical junctures of biological events that confer competence to proceed along their trajectories. These high-plasticity nodes have emerged as central regulators of developmental progression and determinants of disease outcomes, serving as functional bottlenecks in which resolution or persistence dictates normal or maladaptive pathological responses. Recent single-cell and multiomics technologies enabled their detection with unprecedented resolution, revealing conserved regulatory themes, including stress-response activation and striking context dependence shaped by niche cues and tissue architecture. Yet challenges remain in capturing their rapid heterogeneous dynamic in the multiple contexts, and defining their function, in vivo. Here we summarize current concepts on the identification, diversity, role, and regulation of these cell states in events from early development to adult homeostasis, repair, and disease. The increasing recognition that transitional states can be productive conduits or pathological traps underscores their relevance in these processes and potential for the identification of therapeutic targets for intervention in disease, cancer, and regenerative medicine.

Indexed as

Cell DifferentiationRegenerationAnimalsCell LineageHumanscell fatedevelopmentrepair-regenerationstem celltransitional cell state

Identifiers

PMID42012134
PMCPMC13182844

What OpenQuestion holds

Textmetadata
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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.