Erythroferrone contributes to hepcidin repression in a mouse model of malarial anemia Article Swipe
Chloé Latour
,
Myriam F. Wlodarczyk
,
Grace Jung
,
Aurélie Gineste
,
Nicolas Blanchard
,
Tomas Ganz
,
Marie‐Paule Roth
,
Hélène Coppin
,
Léon Kautz
·
YOU?
·
· 2016
· Open Access
·
· DOI: https://doi.org/10.3324/haematol.2016.150227
YOU?
·
· 2016
· Open Access
·
· DOI: https://doi.org/10.3324/haematol.2016.150227
Malaria, a major global health challenge worldwide, is accompanied by a severe anemia secondary to hemolysis and increased erythrophagocytosis. Iron is an essential functional component of erythrocyte hemoglobin and its availability is controlled by the liver-derived hormone hepcidin. We examined the regulation of hepcidin during malarial infection in mice using the rodent parasite Plasmodium berghei K173. Mice infected with Plasmodium berghei K173 develop a severe anemia and die after 18 to 22 days without cerebral malaria. During the early phase of blood-stage infection (days 1 to 5), a strong inflammatory signature was associated with an increased production of hepcidin. Between days 7 and 18, while infection progressed, red blood cell count, hemoglobin and hematocrit dramatically decreased. In the late phase of malarial infection, hepcidin production was reduced concomitantly to an increase in the messenger RNA expression of the hepcidin suppressor erythroferrone in the bone marrow and the spleen. Compared with wild-type mice, Erfe-/- mice failed to adequately suppress hepcidin expression after infection with Plasmodium berghei K173. Importantly, the sustained production of hepcidin allowed by erythroferrone ablation was associated with decreased parasitemia, providing further evidence that transient iron restriction could be beneficial in the treatment of malaria.
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Metadata
- Type
- article
- Language
- en
- Landing Page
- https://doi.org/10.3324/haematol.2016.150227
- http://www.haematologica.org/content/haematol/102/1/60.full.pdf
- OA Status
- gold
- Cited By
- 38
- References
- 48
- Related Works
- 10
- OpenAlex ID
- https://openalex.org/W2522399701
All OpenAlex metadata
Raw OpenAlex JSON
- OpenAlex ID
-
https://openalex.org/W2522399701Canonical identifier for this work in OpenAlex
- DOI
-
https://doi.org/10.3324/haematol.2016.150227Digital Object Identifier
- Title
-
Erythroferrone contributes to hepcidin repression in a mouse model of malarial anemiaWork title
- Type
-
articleOpenAlex work type
- Language
-
enPrimary language
- Publication year
-
2016Year of publication
- Publication date
-
2016-09-22Full publication date if available
- Authors
-
Chloé Latour, Myriam F. Wlodarczyk, Grace Jung, Aurélie Gineste, Nicolas Blanchard, Tomas Ganz, Marie‐Paule Roth, Hélène Coppin, Léon KautzList of authors in order
- Landing page
-
https://doi.org/10.3324/haematol.2016.150227Publisher landing page
- PDF URL
-
https://www.haematologica.org/content/haematol/102/1/60.full.pdfDirect link to full text PDF
- Open access
-
YesWhether a free full text is available
- OA status
-
goldOpen access status per OpenAlex
- OA URL
-
https://www.haematologica.org/content/haematol/102/1/60.full.pdfDirect OA link when available
- Concepts
-
Plasmodium berghei, Hepcidin, Erythropoiesis, Spleen, Anemia, Parasitemia, Erythropoietin, Immunology, Biology, Internal medicine, Hematocrit, Hemoglobin, Endocrinology, Medicine, Malaria, Plasmodium falciparumTop concepts (fields/topics) attached by OpenAlex
- Cited by
-
38Total citation count in OpenAlex
- Citations by year (recent)
-
2025: 3, 2024: 6, 2023: 3, 2022: 2, 2021: 5Per-year citation counts (last 5 years)
- References (count)
-
48Number of works referenced by this work
- Related works (count)
-
10Other works algorithmically related by OpenAlex
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| abstract_inverted_index.hemoglobin | 27, 111 |
| abstract_inverted_index.infection, | 122 |
| abstract_inverted_index.production | 96, 124, 169 |
| abstract_inverted_index.regulation | 41 |
| abstract_inverted_index.suppressor | 139 |
| abstract_inverted_index.worldwide, | 6 |
| abstract_inverted_index.accompanied | 8 |
| abstract_inverted_index.blood-stage | 81 |
| abstract_inverted_index.erythrocyte | 26 |
| abstract_inverted_index.progressed, | 106 |
| abstract_inverted_index.restriction | 187 |
| abstract_inverted_index.Importantly, | 166 |
| abstract_inverted_index.availability | 30 |
| abstract_inverted_index.dramatically | 114 |
| abstract_inverted_index.inflammatory | 89 |
| abstract_inverted_index.parasitemia, | 180 |
| abstract_inverted_index.concomitantly | 127 |
| abstract_inverted_index.liver-derived | 35 |
| abstract_inverted_index.erythroferrone | 140, 174 |
| abstract_inverted_index.Erfe<sup>-/-</sup> | 152 |
| abstract_inverted_index.erythrophagocytosis. | 18 |
| cited_by_percentile_year.max | 99 |
| cited_by_percentile_year.min | 94 |
| countries_distinct_count | 2 |
| institutions_distinct_count | 9 |
| sustainable_development_goals[0].id | https://metadata.un.org/sdg/3 |
| sustainable_development_goals[0].score | 0.8100000023841858 |
| sustainable_development_goals[0].display_name | Good health and well-being |
| citation_normalized_percentile.value | 0.90405595 |
| citation_normalized_percentile.is_in_top_1_percent | False |
| citation_normalized_percentile.is_in_top_10_percent | True |