Fig. 1.
![Fig. 1. Eotaxin-induced [Ca++]ichanges in monocytes. / FURA-2-loaded monocytes were stimulated sequentially at 90-second intervals with 1 μM eotaxin followed by 10 nM MCP-1, 30 nM RANTES, or 10 nM MIP-1β (A) or vice versa (B), and [Ca++]i-dependent fluorescence changes were recorded. The tracings are representative of 2 to 4 independent experiments performed under identical conditions with cells from different donors.](https://ash.silverchair-cdn.com/ash/content_public/journal/blood/97/7/10.1182_blood.v97.7.1920/6/h80710851001.jpeg?Expires=1735576022&Signature=jM1iYESvFvsWZsVHNjUU9W3xfhtFPrJA1F-sRQILPYZwbX-IKswcmkDgu3zJBjJfe6XdiJV603zjZq~3Xf4MbUJvyL4~CXNfMXc-TRteqS9XNnZlDT0oMUwzxBgKw639Mas2UrRxl6f1~ZvdFJP-FGWOx4UhagMdGl0KlY-iVwUj5Ll~ozYU4gUnef8lEzJPB8fefrqCV20aMrpp5KZLzhInIxHz-FgIg~8C5Neb3kuXn4Mp9obM35qAZG721clYylJRYbopWdvMO7ef0u0iSlOEJiCIuBKaQfC3to1wdXg8kMqbE-I5cDlmuxkFbnOaFRrFlAJZzK9QYWxsaIfyNw__&Key-Pair-Id=APKAIE5G5CRDK6RD3PGA)
Eotaxin-induced [Ca++]ichanges in monocytes.
FURA-2-loaded monocytes were stimulated sequentially at 90-second intervals with 1 μM eotaxin followed by 10 nM MCP-1, 30 nM RANTES, or 10 nM MIP-1β (A) or vice versa (B), and [Ca++]i-dependent fluorescence changes were recorded. The tracings are representative of 2 to 4 independent experiments performed under identical conditions with cells from different donors.
