FN Archimer Export Format PT J TI Isolation and primary culture of gill and digestive gland cells from the common mussel Mytilus edulis BT AF FAUCET, Jerome MAURICE, Manuelle GAGNAIRE, Beatrice RENAULT, Tristan BURGEOT, Thierry AS 1:;2:;3:;4:;5:; FF 1:PDG-DEL-PC;2:PDG-DOP-DCN-BE-LBEX;3:PDG-DOP-DCN-AGSAE-LGP;4:PDG-DOP-DCN-AGSAE-LGP;5:PDG-DOP-DCN-BE-LBEX; SI NANTES LA TREMBLADE SE PDG-DEL-PC PDG-DOP-DCN-BE-LBEX PDG-DOP-DCN-AGSAE-LGP TC 0 UR https://archimer.ifremer.fr/doc/2004/publication-936.pdf LA English DT Article DE ;Mytilus edulis;Gill;Flow cytometry;Digestive gland;Cell culture AB As the marine mussel Mytilus edulis is commonly used as a sentinel species, it would be useful to develop a primary culture of the target organs most often in contact with the marine environment. This study reports an improved method for dissociating the digestive gland and gills of M. edulis and considers the effect of mussel storage on cell viability and functionality before culture initiation. Viability and enzymatic activities such as those of esterase and peroxidase were monitored by flow cytometry, a sensitive, objective technique allowing large volumes of cells to be counted within a short time. A primary culture of digestive gland showed more than 75% viability after 72 h. Mussels were maintained in an aquarium containing clean, oxygenated seawater at 12 °C for two days before culture initiation, and dissociation was performed mechanically and chemically with Ca-Mg-free saline to obtain digestive gland cells. Application of nonspecific esterase activity, using fluorescein diacetate (FDA test) coupled with flow cytometry, characterised the functionality of digestive gland and gill cells in culture. PY 2004 SO Methods in Cell Science PU Springer VL 25 IS 3-4 DI 10.1007/s11022-004-8227-4 ID 936 ER EF