Evidence map›Paper›PMID 17148659›Full record

ArticleThe American journal of pathology2006

Role of endocytic inhibitory drugs on internalization of amyloidogenic light chains by cardiac fibroblasts.

Grace Fortes Monis, Christopher Schultz, Ruiyi Ren, Jeremy Eberhard, Catherine Costello, Lawreen Connors, Martha Skinner, Vickery Trinkaus-Randall

Open access · bronzeAbstract read
In one paragraph

Article in The American journal of pathology, 2006. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers.

0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed
1.1field-weighted citation impact, top 26% 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

29 citing papers in PubMed, 55 citations in OpenAlex.

  1. Trial
  2. Article
  3. Review
  4. Serum and Tissue Light-Chains as Disease Biomarkers in AL Amyloidosis.International journal of molecular sciences · 2025
    Review
  5. Review
  6. Review
  7. Future Perspectives.Hematology/oncology clinics of North America · 2020
    Review
  8. Article
  9. Immunoglobulin light chain amyloid aggregation.Chemical communications (Cambridge, England) · 2018
    Review
  10. Article
  11. Article
  12. Article
  13. Article
  14. Review
  15. Review
  16. Article
  17. Article
  18. Systemic amyloidoses.Annual review of biochemistry · 2013
    Review
  19. Article
  20. 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

8 authors at 2 institutions in 1 country.

Grace Fortes MonisDepartment of Pathology, Gerry Amyloid Research Laboratory, Boston University School of Medicine, 80 E. Concord St. L904, Boston, MA 02118, USA.
Christopher Schultz
Ruiyi Ren
Jeremy Eberhard
Catherine Costello
Lawreen Connors
Martha Skinner
Vickery Trinkaus-Randall
Boston University · USAmyloidosis Foundation · US

Funding

XI INTERNATIONAL SYMPOSIUM ON AMYLOIDOSISP41RR010888 · NCRR · BOSTON UNIVERSITY MEDICAL CAMPUS · PI ZAIA, JOSEPH · 1996 to 2011
$18.6M
Tissue response to amyloidogenic light chainsP01HL068705 · NHLBI · BOSTON UNIVERSITY MEDICAL CAMPUS · PI SELDIN, DAVID C · 2002 to 2006
$7.8M
NCRR NIH HHS P41 RR010888NHLBI NIH HHS P01 HL-068705NHLBI NIH HHS P01 HL068705
6 · The paper itself

Abstract

Amyloidosis is a disease of protein misfolding that ultimately impairs organ function. Previously, we demonstrated that amyloidogenic light chains (kappa1, lambda6, and lambda3 subtypes), internalized by cardiac fibroblasts, enhanced sulfation of secreted glycosaminoglycans. In this study, we investigated the internalization and cellular trafficking of urinary immunoglobulin light chains into cardiac fibroblasts. We demonstrate that these light chains have the ability to form annular rings in solution. Internalization was assessed by incubating cells in the presence of light chain conjugated to Oregon Green 488 followed by monitoring with live cell confocal imaging. The rate of light chain internalization was reduced by treatment with methyl-beta-cyclodextrin but not filipin. Amyloid light chain did co-localize with dextran-Texas Red. Once internalized, the light chains were detected in lysosomes and then secreted into the extracellular medium. The light chain detected in the cell lysate and medium possessed a lower hydrophobic species. Nocodazole, a microtubule inhibitor, did not disperse aggregates. In addition, internalization and retention of the light chain proteins was altered in the presence of the proteasomal inhibitor MG132. These results indicate that the cell internalizes light chain by a fluid phase endocytosis, which is then modified and ultimately compromises the cell.

Indexed as

AmyloidAmyloidosisAnimalsCell MembraneCells, CulturedDextransEndocytosisFibroblastsHydrophobic and Hydrophilic InteractionsImmunoglobulin Light ChainsMyocardiumRatsAmyloidDextransImmunoglobulin Light Chains

Identifiers

PMID17148659
PMCPMC1762491
OpenAlexW2000274949

What OpenQuestion holds

Textmetadata
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.