Intracellular localization of the migration inhibitory factor (MIF) in a long term human lymphoid cell line

M. B. Prystowsky, C. F. Sorokin, W. S. Ceglowski, K. Hirschhorn, P. R. Glade

Research output: Contribution to journalArticle

2 Scopus citations

Abstract

Subcellular fractions of the human lymphoid cell line PGLC 33H were obtained by N 2 cavitation and differential centrifugation. The purity of the fractions was assessed by the use of the following marker enzymes: β glucuronidase for the lysosomal intermediate fraction; a nonspecific esterase for the microsomal fraction; and LDH (lactic dehydrogenase) for the supernatant fraction. These subcellular fractions were studied for MIF (migratory inhibition factor) activity, utilizing human lymphoid cells from established lines as target cells. MIF activity was most consistently found in the microsomal fraction. Also, MIF activity was closely associated with the relative specific activity of esterase. No such correlation with MIF activity could be demonstrated for β glucuronidase or LDH.

Original languageEnglish (US)
Pages (from-to)225-235
Number of pages11
JournalInternational Archives of Allergy and Applied Immunology
Volume48
Issue number2
StatePublished - Jan 1 1975
Externally publishedYes

ASJC Scopus subject areas

  • Immunology and Allergy

Fingerprint Dive into the research topics of 'Intracellular localization of the migration inhibitory factor (MIF) in a long term human lymphoid cell line'. Together they form a unique fingerprint.

  • Cite this