Evidence map›Paper›PMID 35452314›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2022

Protein and lipid mass concentration measurement in tissues by stimulated Raman scattering microscopy.

Seungeun Oh, ChangHee Lee, Wenlong Yang, Ang Li, Avik Mukherjee, Markus Basan, Chongzhao Ran, Wei Yin, Clifford J Tabin, Dan Fu and 2 more

Open access · greenAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 71 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
71citing papers in PubMed, 1 pooled it
25.6field-weighted citation impact, top 1% 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

71 citing papers in PubMed, 1 synthesis or guideline pooled it, 99 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Article
  4. PLANCK: super-multiplex optical imaging without labeling.bioRxiv : the preprint server for biology · 2026
    Article
  5. Review
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  10. Review
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  14. Review
  15. Article
  16. Article
  17. Review
  18. Article
  19. Normalized Raman Imaging for Studies of Tissue Physiology of the Kidney.bioRxiv : the preprint server for biology · 2025
    Article
  20. Imaging Cellular Metabolic Rewiring with SuMMIT-SRS.bioRxiv : the preprint server for biology · 2025
    Article

11 more citing papers are in PubMed but not listed here.

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

12 authors at 3 institutions in 2 countries.

Seungeun OhDepartment of Systems Biology, Harvard Medical School, Boston, MA 02115.ORCID 0000-0002-4064-9301
ChangHee LeeDepartment of Genetics, Harvard Medical School, Boston, MA 02115.
Wenlong YangCenter for Advanced Imaging, Harvard University, Cambridge, MA 20138.
Ang LiDepartment of Systems Biology, Harvard Medical School, Boston, MA 02115.
Avik MukherjeeDepartment of Systems Biology, Harvard Medical School, Boston, MA 02115.
Markus BasanDepartment of Systems Biology, Harvard Medical School, Boston, MA 02115.
Chongzhao RanAthinoula A. Martinos Center for Biomedical Imaging, Massachusetts General Hospital and Harvard Medical School, Boston, MA 02129.ORCID 0000-0002-3892-4108
Wei YinAthinoula A. Martinos Center for Biomedical Imaging, Massachusetts General Hospital and Harvard Medical School, Boston, MA 02129.
Clifford J TabinDepartment of Genetics, Harvard Medical School, Boston, MA 02115.
Dan FuDepartment of Chemistry, University of Washington, Seattle, WA 98195.ORCID 0000-0001-9243-8306
X Sunney XieBiomedical Pioneering Innovation Center, Peking University, Beijing 100871; China.
Marc W KirschnerDepartment of Systems Biology, Harvard Medical School, Boston, MA 02115.ORCID 0000-0001-6540-6130
Harvard University · USPeking University · CNUniversity of Washington · US

Funding

BIOCHEMICAL STUDIES OF MITOSISR01GM026875 · NIGMS · UNIVERSITY OF CALIFORNIA SAN FRANCISCO · PI KIRSCHNER, MARC WALLACE · 1985 to 2019
$18.2M
Reverse Engineering of Cell SenescenceR01AG073341 · NIA · HARVARD MEDICAL SCHOOL · PI MARC Wallace KIRSCHNER · 2022 to 2026
$3.3M
Elucidating physiology of dormant bacteria to combat antibiotic persistenceR35GM137895 · NIGMS · HARVARD MEDICAL SCHOOL · PI Markus Thomas Basan · 2020 to 2026
$3.2M
Near infrared fluorescence imaging of reactive oxygen species in Alzheimer's diseaseR01AG055413 · NIA · MASSACHUSETTS GENERAL HOSPITAL · PI RAN, CHONGZHAO · 2018 to 2022
$2.1M
In vivo Handheld Coherent Raman Scattering (CRS) Microscopy for Glioma ImagingR01EB017254 · NIBIB · HARVARD UNIVERSITY · PI ORRINGER, DANIEL, XIE, XIAOLIANG SUNNEY · 2014 to 2018
$1.9M
NIA NIH HHS R01 AG055413NIA NIH HHS R01 AG073341NIBIB NIH HHS R01 EB017254NIGMS NIH HHS R01 GM026875NIGMS NIH HHS R35 GM137895
6 · The paper itself

Abstract

Cell mass and chemical composition are important aggregate cellular properties that are especially relevant to physiological processes, such as growth control and tissue homeostasis. Despite their importance, it has been difficult to measure these features quantitatively at the individual cell level in intact tissue. Here, we introduce normalized Raman imaging (NoRI), a stimulated Raman scattering (SRS) microscopy method that provides the local concentrations of protein, lipid, and water from live or fixed tissue samples with high spatial resolution. Using NoRI, we demonstrate that protein, lipid, and water concentrations at the single cell are maintained in a tight range in cells under the same physiological conditions and are altered in different physiological states, such as cell cycle stages, attachment to substrates of different stiffness, or by entering senescence. In animal tissues, protein and lipid concentration varies with cell types, yet an unexpected cell-to-cell heterogeneity was found in cerebellar Purkinje cells. The protein and lipid concentration profile provides means to quantitatively compare disease-related pathology, as demonstrated using models of Alzheimer’s disease. This demonstration shows that NoRI is a broadly applicable technique for probing the biological regulation of protein mass, lipid mass, and water mass for studies of cellular and tissue growth, homeostasis, and disease.

Indexed as

Nonlinear Optical MicroscopySpectrum Analysis, RamanLipid MetabolismLipidsMicroscopyProteinsLipidsProteinscell sizelipid imagingquantitative microscopysingle cell mass quantificationstimulated Raman scattering

Identifiers

PMID35452314
PMCPMC9169924
OpenAlexW4225701840

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.