Evidence map›Paper›PMID 29401392›Full record

ArticleAnalytical chemistry2018

Label-Free Imaging of Heme Dynamics in Living Organisms by Transient Absorption Microscopy.

Andy Jing Chen, Xiaojing Yuan, Junjie Li, Puting Dong, Iqbal Hamza, Ji-Xin Cheng

Abstract read
In one paragraph

Article in Analytical chemistry, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
2.2field-weighted citation impact, top 11% 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

16 citing papers in PubMed, 38 citations in OpenAlex.

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  10. Leaving the Limits of Linearity for Light Microscopy.The journal of physical chemistry. C, Nanomaterials and interfaces · 2020
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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

6 authors at 3 institutions in 1 country.

Andy Jing ChenDepartment of Biological Sciences , Purdue University , West Lafayette , Indiana 47907 , United States.
Xiaojing YuanDepartment of Animal & Avian Sciences , University of Maryland , College Park , Maryland 20742 , United States.
Junjie LiDepartment of Electrical & Computer Engineering , Boston University , Boston , Massachusetts 02215 , United States.
Puting DongDepartment of Chemistry , Boston University , Boston , Massachusetts 02215 , United States.
Iqbal HamzaDepartment of Animal & Avian Sciences , University of Maryland , College Park , Maryland 20742 , United States.
Ji-Xin ChengDepartment of Electrical & Computer Engineering , Boston University , Boston , Massachusetts 02215 , United States.ORCID 0000-0002-5607-6683
Boston University · USUniversity of Maryland, College Park · USPurdue University West Lafayette · US

Funding

Proteomics CoreU54DK110858 · NIDDK · UTAH STATE HIGHER EDUCATION SYSTEM--UNIVERSITY OF UTAH · PI Anna E Beaudin, JAMES Eric COX · 2016 to 2026
$8.6M
The Biological Role of Heme in NutritionR01DK074797 · NIDDK · UNIV OF MARYLAND, COLLEGE PARK · PI Iqbal Hamza · 2006 to 2026
$5.4M
Molecular Determinants of Intracellular Survival and Replication in LeishmaniaR01AI067979 · NIAID · YALE UNIVERSITY · PI ANDREWS, NORMA WINDSOR · 2007 to 2018
$3.8M
The Transport of Nutritional Heme in Animal DevelopmentR01DK085035 · NIDDK · UNIV OF MARYLAND, COLLEGE PARK · PI HAMZA, IQBAL · 2010 to 2019
$3.6M
Imaging heme based mitochondrial-cell signaling networks in cell and animal modelR33ES025661 · NIEHS · GEORGIA INSTITUTE OF TECHNOLOGY · PI REDDI, AMIT RAM · 2017 to 2019
$1.7M
Microsecond Raman spectroscopy: Assessing single cell metabolism in a vital organismR21GM114853 · NIGMS · PURDUE UNIVERSITY · PI CHENG, JI-XIN · 2014 to 2015
$449k
NIAID NIH HHS R01 AI067979NIDDK NIH HHS R01 DK074797NIDDK NIH HHS R01 DK085035NIDDK NIH HHS U54 DK110858NIEHS NIH HHS R33 ES025661NIGMS NIH HHS R21 GM114853
6 · The paper itself

Abstract

Heme, a hydrophobic and cytotoxic macrocycle, is an essential cofactor in a large number of proteins and is important for cell signaling. This must mean that heme is mobilized from its place of synthesis or entry into the cell to other parts of the cell where hemoproteins reside. However, the cellular dynamics of heme movement is not well understood, in large part due to the inability to image heme noninvasively in live biological systems. Here, using high-resolution transient absorption microscopy, we showed that heme storage and distribution is dynamic in Caenorhabditis elegans. Intracellular heme exists in concentrated granular puncta which localizes to lysosomal-related organelles. These granules are dynamic, and their breaking down into smaller granules provides a mechanism by which heme stores can be mobilized. Collectively, these direct and noninvasive dynamic imaging techniques provide new insights into heme storage and transport and open a new avenue for label-free investigation of heme function and regulation in living systems.

Indexed as

AnimalsCaenorhabditis elegansHEK293 CellsHemeHumansLysosomesMicroscopyOptical ImagingHeme

Identifiers

PMID29401392
PMCPMC5972037
OpenAlexW2790265768

What OpenQuestion holds

Textmetadata
LicenceTDM
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.