Evidence map›Paper›PMID 40501913›Full record

ArticlebioRxiv : the preprint server for biology2025

Finding signatures of low-dimensional geometric landscapes in high-dimensional cell fate transitions.

Maria Yampolskaya, Laertis Ikonomou, Pankaj Mehta

Abstract readPreprint
In one paragraph

Article in bioRxiv : the preprint server for biology, 2025. 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

3 authors.

Maria YampolskayaDepartment of Physics, Boston University, Boston, MA 02215, USA.ORCID 0000-0003-2941-2589
Laertis IkonomouDepartment of Oral Biology, University at Buffalo School of Dental Medicine, Buffalo, NY 14215, USA Cell, Gene and Tissue Engineering Center, University at Buffalo, Buffalo, NY 14260, USA and Chemical and Biological Engineering Department, University at Buffalo, Buffalo, NY 14260, USA.ORCID 0000-0003-0993-6713
Pankaj MehtaDepartment of Physics, Boston University, Boston, MA 02215, USA Center for Regenerative Medicine of Boston University and Boston Medical Center, Boston, MA 02215, USA.ORCID 0000-0003-1290-5897

Funding

MODELING EMERGENT BEHAVIORS IN SYSTEMS BIOLOGY: A BIOLOGICAL PHYSICS APPROACHR35GM119461 · NIGMS · BOSTON UNIVERSITY (CHARLES RIVER CAMPUS) · PI Pankaj Mehta · 2016 to 2026
$3.6M
NIGMS NIH HHS R35 GM119461
6 · The paper itself

Abstract

Multicellular organisms develop a wide variety of highly-specialized cell types. The consistency and robustness of developmental cell fate trajectories suggests that complex gene regulatory networks effectively act as low-dimensional cell fate landscapes. A complementary set of works draws on the theory of dynamical systems to argue that cell fate transitions can be categorized into universal decision-making classes. However, the theory connecting geometric landscapes and decision-making classes to high-dimensional gene expression space is still in its infancy. Here, we introduce a phenomenological model that allows us to identify gene expression signatures of decision-making classes from single-cell RNA-sequencing time-series data. Our model combines low-dimensional gradient-like dynamical systems and high-dimensional Hopfield networks to capture the interplay between cell fate, gene expression, and signaling pathways. We apply our model to the maturation of alveolar cells in mouse lungs to show that the transient appearance of a mixed alveolar type 1/type 2 state suggests the triple cusp decision-making class. We also analyze lineage-tracing data on hematopoetic differentiation and show that bipotent neutrophil-monocyte progenitors likely undergo a heteroclinic flip bifurcation. Our results suggest it is possible to identify universal decision-making classes for cell fate transitions directly from data.

Identifiers

PMID40501913
PMCPMC12154842

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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.