Wittrup:Making a cell line from tumor sections: Difference between revisions

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(New page: *Protocol courtesy of Leah Schmidt, Jacks Lab @MIT* Reagents: Collagenase Type IV Worthington Biochemical Corp ls004186 Hyaluronidase Worthington Biochemical Corp ls002594 Collagenase Ty...)
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Revision as of 11:06, 16 August 2012

  • Protocol courtesy of Leah Schmidt, Jacks Lab @MIT*

Reagents:

Collagenase Type IV Worthington Biochemical Corp ls004186 Hyaluronidase Worthington Biochemical Corp ls002594 Collagenase Type I Worthington Biochemical Corp ls004194 Collagenase/Dispase Roche 10269 638001

1. Finely dice tumors in plastic dishes without media, then transfer to a 15 ml Falcon tube (no filter yet) 2. Add 2 mL digestion media/tumor: For FACS samples, 125 U/ml Collagenase Type IV, 60 U/ml Hyaluronidas in PBS or RPMI + 1% serum; for cell lines, 125 U/ml Collagenase Type I, 60 U/ml Hyaluronidase, 2 mg/ml Collagenase/Dispase in PBS or RPI + 1% serum (can also add gentamicin for cell lines) NOTE: Collagenase type I and Dispase tend to remove surface proteins, so don't use those for FACS samples 3. Incubate in digestion media ~ 1 hr on 37°C shaker, then pass the cells over a cell strainer 4. Wash with PBS and plate cells in DMEM+gentamicin, pen-strep, and 10% FBS 5. Next day, change media (gently) 6. In a few days to weeks, cells should grow out amidst many dead/senescent cells. Passage them until they look somewhat uniform.