ArticleThe Journal of clinical investigation1977
Eosinophilopoietin. A circulating low molecular weight peptide-like substance which stimulates the production of eosinophils in mice.
Article in The Journal of clinical investigation, 1977. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.
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Who cites it
10 citing papers in PubMed.
- Hypereosinophilia in a horse with intestinal lymphosarcoma.The Canadian veterinary journal = La revue veterinaire canadienne · 1997Article
- Extramedullary eosinophilopoiesis in the liver of Schistosoma japonicum-infected mice, with reference to hemopoietic stem cells.Parasitology research · 1990Article
- Severe eosinophilia associated with a malignant islet cell tumour.CMAJ : Canadian Medical Association journal = journal de l'Association medicale canadienne · 1989Article
- The effect of eosinophil chemotactic factors on in vitro eosinopoiesis in the guinea pig.Blut · 1983Article
- Enhancement of human eosinophil-mediated killing of Schistosoma mansoni larvae by mononuclear cell products in vitro.The Journal of experimental medicine · 1983Article
- Genetic control of eosinophilia. Mouse strain variation in response to antigens of parasite origin.Clinical and experimental immunology · 1983Article
- Eosinophilic gastroenteritis with rectal involvement: case report and a review of literature.Journal of the National Medical Association · 1981Review
- Review
- Human erythroid burst-forming unit: T-cell requirement for proliferation in vitro.The Journal of experimental medicine · 1978Article
- Age-related changes in the manifestations of tuberculosis. Implications for drug therapy.Drugs & agingReview
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Authors and funding
3 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
In earlier studies, methods were developed to raise specific antibodies in rabbits against purified suspensions of mouse or human eosinophils. On administration of antieosinophil serum (AES) to mice, the mature eosinophils in tissues, peripheral blood, and bone marrow were depleted, while the immature eosinophil pool in the bone marrow was observed to proliferate. The current investigations explore the generation of eosinophilopoietic factors during AES-induced eosinophilopenia. Mice received three injections of AES, one every other day. As the peripheral eosinophil counts started to recover after the last AES injection, the serum was collected and transferred to normal animals. Within 2 days the recipients showed an increase in peripheral blood as well as in bone marrow eosinophils. The rise in bone marrow eosinophils was due to newly formed cells as evidenced by increased uptake of [(3)H]thymidine. The generation of eosinophilopoietic activity was specifically related to depletion of eosinophils but not neutrophils. The eosinophilopoietic activity was: (a) dependent on the volume of serum transferred, (b) lost on dialysis, and (c) largely heat labile. The activity eluted as a low molecular weight substance on G-25 Sephadex and was digested by pronase but not by trypsin. Active fractions collected from G-25 columns were not chemotactic for the eosinophils in vitro. Thus, specific depletion of mature eosinophils generates a low molecular weight peptide which stimulates eosinophilopoiesis in vivo. It is suggested that this substance be named eosinophilopoietin.
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