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Updated: Mar 6, 2026

Direct Lineage Reprogramming of Adult Mouse Fibroblast to Erythroid Progenitors
Published on: December 14, 2018
The metamorphic switch in hemoglobin phenotype ofXenopus laevis involves erythroid cell replacement.
Rudolf Weber1, Marianne Geiser1, Peter Müller1
1Abteilung für Zell-und Entwicklungsbiologie, Zoologisches Institut, Baltzerstrasse 4, CH-3012, Bern, Switzerland.
Hemoglobin transition in Xenopus laevis involves replacing larval red blood cells with adult ones. This shift occurs as larval cell renewal stops, indicating a developmental switch in erythropoiesis.
Area of Science:
- Developmental Biology
- Hematology
- Xenopus laevis Research
Background:
- Metamorphosis in Xenopus laevis involves significant physiological changes, including a switch in hemoglobin types.
- Understanding the cellular mechanisms of hemoglobin transition is crucial for comprehending amphibian development.
Purpose of the Study:
- To investigate the cellular basis of hemoglobin transition during Xenopus laevis metamorphosis.
- To determine if hemoglobin transition is due to cellular replacement or changes within existing erythrocytes.
Main Methods:
- Indirect immunofluorescence was used to analyze the distribution of larval and adult hemoglobins in circulating erythrocytes.
- Erythrocyte morphology, DNA synthesis, and hemoglobin synthesis were monitored throughout metamorphosis.
Main Results:
- Larval and adult hemoglobins were found to be localized in distinct erythrocyte populations.
- Hemoglobin transition correlated with the replacement of larval erythrocytes by new cells synthesizing adult globin.
- The process was not accompanied by an increase in immature erythroid cells, suggesting advanced maturation of new cells.
Conclusions:
- Hemoglobin transition in Xenopus laevis is primarily mediated by the replacement of larval erythrocytes with adult-committed cells.
- Cessation of DNA synthesis and larval hemoglobin production in the larval erythrocyte population is a key event.
- Presumptive adult erythroid cells likely enter circulation at a more mature stage.
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