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=1722431976&Signature=1~QWPaqEoYHyLKHqt~jBGo70B4v3dX65BCc84uaqsvj2v9RMJRKulGgTjsyo6Tr4nmtqgk3bU~WcpXD2FQSVOqQD8v0d9U8BshPJBbdLxKldar3Ph5G~9ov7tZzJrkMSRUSmXsrKfc4rAR9JlswEf4xLzr5B24HgdDtOFCwoM2NQoSOx7eITXjm0ZTByqa-oC71ReU3jUVEWWYqxmPZaGH4IU7rfFOjYasgFJ4w6FCCLnMIQqfyGCebIe~W59Kl8E3A0DiFqnS~mii9BnR0QvqrXqj0F4XNNgu~vH3kxYwCBb0LLKMAvV8a8dSTCEOc2RjBVv1CtDne-sLZO6q~AhQ__&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.
