Evidence map›Paper›PMID 39190102›Full record

ArticleCellular and molecular life sciences : CMLS2024

Notch transcriptional target tmtc1 maintains vascular homeostasis.

Na Yoon Paik, Jacob Neethling, Mumtaz Anwar, Prerak Gupta, Mark A Sanborn, Zekun Shen, Thilinie Bandara, James Hyun, L A Naiche, Jan K Kitajewski and 4 more

Abstract read
In one paragraph

Article in Cellular and molecular life sciences : CMLS, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. Article
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

14 authors.

Na Yoon PaikDepartment of Pharmacology and Regenerative Medicine, University of Illinois at Chicago College of Medicine, Chicago, IL, 60612, USA.
Jacob NeethlingDepartment of Pharmacology and Regenerative Medicine, University of Illinois at Chicago College of Medicine, Chicago, IL, 60612, USA.
Mumtaz AnwarDepartment of Pharmacology and Regenerative Medicine, University of Illinois at Chicago College of Medicine, Chicago, IL, 60612, USA.
Prerak GuptaDepartment of Pharmacology and Regenerative Medicine, University of Illinois at Chicago College of Medicine, Chicago, IL, 60612, USA.
Mark A SanbornDepartment of Biochemistry, University of Illinois at Chicago College of Medicine, Chicago, IL, USA.
Zekun ShenDepartment of Pharmacology and Regenerative Medicine, University of Illinois at Chicago College of Medicine, Chicago, IL, 60612, USA.
Thilinie BandaraDepartment of Pharmacology and Regenerative Medicine, University of Illinois at Chicago College of Medicine, Chicago, IL, 60612, USA.
James HyunDepartment of Pharmacology and Regenerative Medicine, University of Illinois at Chicago College of Medicine, Chicago, IL, 60612, USA.
L A NaicheDepartment of Physiology and Biophysics, University of Illinois College of Medicine, Chicago, IL, 60612, USA.
Jan K KitajewskiDepartment of Physiology and Biophysics, University of Illinois College of Medicine, Chicago, IL, 60612, USA.
Jalees RehmanDepartment of Biochemistry, University of Illinois at Chicago College of Medicine, Chicago, IL, USA.
Jae-Won ShinDepartment of Pharmacology and Regenerative Medicine, University of Illinois at Chicago College of Medicine, Chicago, IL, 60612, USA.
Dolly MehtaDepartment of Pharmacology and Regenerative Medicine, University of Illinois at Chicago College of Medicine, Chicago, IL, 60612, USA.
Kostandin V PajciniDepartment of Pharmacology and Regenerative Medicine, University of Illinois at Chicago College of Medicine, Chicago, IL, 60612, USA. kvp@uic.edu.ORCID http://orcid.org/0000-0001-7920-3318

Funding

Notch in Angiogenesis and Vascular BiologyR01HL112626 · NHLBI · UNIVERSITY OF ILLINOIS AT CHICAGO · PI Jan K. Kitajewski · 2012 to 2026
$6.3M
Training Core for Chicago KUH FORWARDTL1DK132769 · NIDDK · NORTHWESTERN UNIVERSITY AT CHICAGO · PI Tamara Isakova · 2021 to 2026
$4.0M
NOTCH FUNCTION IN VASCULAR BIOLOGY AND ANGIOGENESISR01HL062454 · NHLBI · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI KITAJEWSKI, JAN K. · 1999 to 2010
$3.4M
Mechanisms and Treatment of SARS-CoV-2 induced Lung Endothelial InjuryR01HL162308 · NHLBI · UNIVERSITY OF ILLINOIS AT CHICAGO · PI REHMAN, JALEES, RICHNER, JUSTIN · 2022 to 2025
$2.9M
iPSC-Derived Vascularized Human Lung Organoids and Interaction Between Lung Endothelial Cells and Alveolar Epithelial CellsR01HL163978 · NHLBI · UNIVERSITY OF ILLINOIS AT CHICAGO · PI KADUR LAKSHMINARASIM, PREETISH, REHMAN, JALEES · 2022 to 2025
$2.9M
The role of Notch signaling in fetal hematopoietic stem cellsR01HL134971 · NHLBI · UNIVERSITY OF ILLINOIS AT CHICAGO · PI PAJCINI, KOSTANDIN · 2017 to 2021
$2.2M
Encapsulation of mesenchymal stromal cells in engineered microgels for resolution of lung fibrosisR01HL141255 · NHLBI · UNIVERSITY OF ILLINOIS AT CHICAGO · PI SHIN, JAE-WON · 2019 to 2023
$2.0M
Engineering microscale hydrogel deposition to direct single stem cell differentiationR01GM141147 · NIGMS · UNIVERSITY OF ILLINOIS AT CHICAGO · PI SHIN, JAE-WON · 2021 to 2024
$1.9M
Therapeutic nanoscale matrimeresR01EB034507 · NIBIB · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI SHIN, JAE-WON · 2023 to 2025
$1.3M
Engineering extracellular vesicles for therapeutic receptor activationR01HL171590 · NHLBI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI Kostandin Pajcini, Jae-Won Shin · 2024 to 2026
$1.1M
A bio-engineered hepatic niche for ex vivo expansion of HSCsR01HL151720 · NHLBI · UNIVERSITY OF ILLINOIS AT CHICAGO · PI KHETANI, SALMAN R, PAJCINI, KOSTANDIN · 2021 to 2023
$959k
Notch signaling regulates stem cell function in the fetal liver hematopoietic nicheR01DK137093 · NIDDK · UNIVERSITY OF ILLINOIS AT CHICAGO · PI Kostandin Pajcini · 2024 to 2026
$929k
NHLBI Division of Intramural Research R01HL151720NHLBI NIH HHS R01 HL062454NHLBI NIH HHS R01 HL112626NHLBI NIH HHS R01 HL134971NHLBI NIH HHS R01HL134971NHLBI NIH HHS R01 HL141255NHLBI NIH HHS R01 HL151720NHLBI NIH HHS R01 HL162308NHLBI NIH HHS R01 HL163978NHLBI NIH HHS R01 HL171590NIBIB NIH HHS R01 EB034507NIDDK NIH HHS R01 DK137093NIDDK NIH HHS TL1 DK132769NIGMS NIH HHS R01 GM141147
6 · The paper itself

Abstract

Proper lung function requires the maintenance of a tight endothelial barrier while simultaneously permitting the exchange of macromolecules and fluids to underlying tissue. Disruption of this barrier results in an increased vascular permeability in the lungs, leading to acute lung injury. In this study, we set out to determine whether transcriptional targets of Notch signaling function to preserve vascular integrity. We tested the in vivo requirement for Notch transcriptional signaling in maintaining the pulmonary endothelial barrier by using two complementary endothelial-specific Notch loss-of-function murine transgenic models. Notch signaling was blocked using endothelial-specific activation of an inhibitor of Notch transcriptional activation, Dominant Negative Mastermindlike (DNMAML; CDH5Cre

Indexed as

Antigens, CDCadherinsEndothelial CellsHomeostasisLungSignal TransductionAdherens JunctionsAnimalsCadherin 5Capillary PermeabilityHumansMiceMice, Inbred C57BLMice, TransgenicReceptor, Notch1Receptors, NotchAntigens, CDCadherin 5CadherinsReceptor, Notch1Receptors, NotchEndothelial cellsNotch signalingVascular permeability

Identifiers

PMID39190102
PMCPMC11349727

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.