Evidence map›Paper›PMID 42681429›Full record

ArticleMethods in molecular biology (Clifton, N.J.)2026

Assessing the Impact of Intravascular Hemolysis on Erythropoiesis in Sickle Cell Disease.

Huan Zhang, Xiuli An

Abstract read
PubMed Publisher
In one paragraph

Article in Methods in molecular biology (Clifton, N.J.), 2026. 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

2 authors.

Huan ZhangSchool of Life Sciences, Zhengzhou University, Zhengzhou, Henan, People's Republic of China.
Xiuli AnLaboratory of Membrane Biology, New York Blood Center, New York, NY, USA. xan@nybc.org.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Intravascular hemolysis is a hallmark of sickle cell disease (SCD). While it has been well established that the hemolysis-derived products, such as hemoglobin (Hb) and free heme, exert proinflammatory and pro-oxidative effects, contributing to the vascular and tissue damage in SCD, the effects of hemolysis on erythropoiesis have not been studied. We and others have reported that hemolysis in SCD led to upregulation of type I interferon IFNα. We further documented that the ability of Townes sickle mice to increase their erythropoietic capacity to compensate for anemia was impaired. To examine whether the impaired erythropoiesis in SCD is associated with the hemolysis-driven IFNα production and to define the underlying mechanisms, we injected mice with hemin, red cell lysate, or IFNα to mimic the hemolysis status in SCD and then examined erythropoiesis by colony-forming assay, flow cytometric analysis, and western blot. We also examined the effects of hemin and IFNα on erythropoiesis using an in vitro erythroid culture system. We found that intravascular hemolysis inhibited erythropoiesis in SCD through inhibition of erythropoietin (EPO)/erythropoietin receptor (EPOR) signaling via a heme-IFNα-CISH axis. Herein, we describe how to prepare hemin, red cell lysate, and IFNα, and present examples of in vivo and in vitro assays to assess erythropoiesis. Our methods can be applied to study changes in erythropoiesis in other diseases characterized by intravascular hemolysis.

Indexed as

Anemia, Sickle CellErythropoiesisHemolysisAnimalsDisease Models, AnimalErythrocytesErythropoietinHemeHeminHumansInterferon-alphaMiceErythropoietinHemeHeminInterferon-alphaEPO/EPORErythropoiesisFree hemeIFNαIntravascular hemolysisSickle cell disease

Identifiers

What Socratic 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 Socratic graph.