Serum-free animal cell culture medium and methods for the primary culture and production of cell lines using this medium

Claim 2

Serum-free animal cell culture medium, characterized in that is consists essentially of: (a) a synthetic basal medium designed for animal cell culture; (b) 0.05 to 30 μeq/l of a mixture of the six fatty acids palmitic acid, cis-palmitoleic acid, stearic acid, cis-oleic acid, cis-linoleic acid and cis-linolenic acid or their esters, in the following proportions, relative to the free fatty acid: from 0.0155 to 24.0 μmole/l of palmitic acid; from 0.0058 to 9.0 μmole/l of cis-palmitoleic acid; from 0.0014 to 2.0 μmole/l of stearic acid; from 0.0067 to 10.0 μmole/l of cis-oleic acid; from 0.0178 to 27.0 μmole/l of cis-linolenic acid; and from 0.0028 to 4.0 μmole/l of cis-linolenic acid, adsorbed on (c) at least one water-soluble lipophile biopolymer present in an amount capable of ensuring the dissolution of the fatty acids or esters present in the medium.

Claim 3

Culture medium according to claim 1, wherein the mixture is of said six fatty acids are present therein in the free acid state.

Claim 4

Culture medium according to claim 1, wherein the synthetic basal medium is selected from the group consisting of: Ham media Waymouth MB 752/1 medium RPMI 1629 or 1640 media Eagle medium modified Eagle media Williams E medium medium 199 and derived media of the types MEM and MEMα.

Claim 5

Culture medium according to claim 1, wherein said antibiotic has a wide spectrum.

Claim 6

Culture medium according to claim 1, wherein said antibiotic is gentamicin in the proportion of 25 to 100 mg/l.

Claim 7

Culture medium according to claim 1, wherein the water soluble lipophile biopolymer is constituted by lipid-free or not lipid-free albumin or by a dextran.

Claim 8

Culture medium according to claim 6, wherein the albumin is present in an amount of 2 to 6 g/l of culture medium.

Claim 9

Culture medium according to claim 6, wherein the dextran is present in an amount from 0.5 to 200 mg/l of culture medium.

Claim 10

Process for obtaining a cell line using the culture medium according to claim 1, which consists of: (a) subjecting to enzymatic digestion the cellular product of a prior culture, to initiate one or several secondary culture(s), (b) carrying out the one or more secondary culture(s) in the culture medium, and (c) repeating steps (a) and (b) with the cellular product of the preceding step (b) as many times as necessary to preserve the cell line during the desired time.

Claim 11

Process for obtaining a cell line according to claim 9, wherein the cellular product results of a prior culture which as reached confluency.

Claim 12

Culture medium according to claim 1 further including an antibiotic in non-cytotoxic concentration throughout the passage of the culture.

Claim 13

Culture medium according to claim 1 further including at least one compound selected from hormones and growth factors.

Claim 14

Culture medium according to claim 12 further including an antibiotic in non-cytotoxic concentration throughout the passage of the culture.

Claim 15

A process for obtaining a cell line using the culture medium according to claim 13, which consists essentially of: (a) suspending cells of a prior culture in the said culture medium; (b) carrying out the culture of the cells in the said culture medium; and (c) repeating steps (a) and (b) as many times as necessary to preserve the cell line during the desired time.

Claim 16

Process for the primary culture of rat liver epithelial cells using the culture medium according to claim 1, characterized in that it consists essentially of: (1) taking up the tissue containing the cells to be cultivated and mincing it very finely, in a basal culture medium, not containing Ca 2+ and Mg 2+ ions, warmed (30°-37° C.), under aseptic conditions; (2) after rinsing, in the basal medium not containing Ca 2+ and Mg 2+ ions, subjecting the tissue to a sequential enzymatic digestion, (3) transferring the suspension of cells thus released into a basal culture medium, centrifuging while following in parallel the digestion of the remaining tissue in step 2, (4) placing the centrifugation pellet in suspension in the culture medium then, (5) inoculating the suspension so obtained on the culture substratum previously or simultaneously surfacted, (6) incubating in an air-tight incubator, saturated with water vapour, in the presence of a nitrogen, oxygen, and carbon dioxide mixture at 76%:19%:5%, while renewing the culture medium periodically, steps (3) to (6) being repeated on the different fractions of dissociated desired cells, obtained sequentially at step (2), using each time a new culture substratum.

Claim 17

A process according to claim 15 wherein, in step (4), the culture medium contains a surface coating agent for the culture substratum.

Claim 18

Process of primary culture of rat liver epithelial cells according to claim 15, characterized in that the enzymatic digestion is carried out by means of collagenase or trypsin.

Claim 19

Process of primary culture of rat liver epithelial cells according to claim 15, characterized in that the surfacting of the substratum is carried out by means of serum, collagen, polylysine or fibronectine.

Claim 20

Process according to claim 18, wherein the surface coating agent of the substratum is fetal calf serum, newborn calf serum or fibronectin.

Claim 21

Process of primary culture of rat liver epithelial cells according to claim 15, wherein the basal culture medium is that used in the preparation of the culture medium of step (4).