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Quail Fetal Antigen (QFA): Identification and comparison with chicken fetal antigen

  • M. A. Qureshi
  • , K. A. Trembicki
  • , J. V. Jackson
  • , P. E. Borenstein
  • , R. R. Dietert

Research output: Contribution to journalArticlepeer-review

4 Scopus citations

Abstract

Quail fetal antigen (QFA), an analogous hematopoietic antigen to chicken fetal antigen (CFA), was identified and shown to be a developmental antigen on the blood cells of Japanese quail and other avian species. Rabbit antiserum against 14-day embryonic quail red blood cells (RBCs) was specifically adsorbed to achieve fetal specificity and to eliminate any cross reactivity with the CFA system. Complement-mediated microcytotoxicity and hemagglutination assays were used to detect the presence of QFA on hematopoietic cells. QFA was found on 100% of the peripheral RBCs from 10-day quail embryos but incidence of the antigen gradually declined with increasing development. Complete loss of QFA from RBCs occurred just prior to sexual maturation between 31 and 42 days of age. No qualitative differences in erythroid expression of QFA were observed during development; however, RBCs from both embryonic duck and interspecific quail- chicken hybrids reacted with R-anti QFA. Like CFA, quail fetal antigen was associated with lymphocytes, particularly those from primary lymphoid organs. Similarities in the developmentally controlled tissue distribution of QFA and CFA suggest that developmental hematopoietic antigens are a common feature of avian species and are useful cell surface markers for studies of development and differentiation.

Original languageEnglish
Pages (from-to)325-331
Number of pages7
JournalDevelopmental and Comparative Immunology
Volume7
Issue number2
DOIs
StatePublished - 1983

Funding

The authors thank Drs. S.E. Bloom, W. Dean, K. Keshavares, C. Walcott, and Mr. I. Reed for supplying and transporting biological materials. Drs. S.G. Campbell and K.A. Schat are gratefully acknowledged for their helpful discussions. Technical assistance provided by Forrest Sanders and Diann Hartwell is greatly appreciated. The assistance of Tom Grant in the production of interspecific hybrids and Diane Colf and Connie Gow in the preparation of this manuscript is gratefully acknowledged. Supported by NSF grant PCM 8109810 and NY(C)157424 from the USDA.

FundersFunder number
National Science Foundation Arctic Social Science Program157424, PCM 8109810
U.S. Department of Agriculture

    ASJC Scopus subject areas

    • Immunology
    • Developmental Biology

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