PRIMARY HUMAN MUSCLE SATELLITE CELL-CULTURE - VARIATIONS OF CELL YIELD, PROLIFERATION AND DIFFERENTIATION RATES ACCORDING TO AGE AND SEX OFDONORS, SITE OF MUSCLE BIOPSY, AND DELAY BEFORE PROCESSING

Citation
S. Bonavaud et al., PRIMARY HUMAN MUSCLE SATELLITE CELL-CULTURE - VARIATIONS OF CELL YIELD, PROLIFERATION AND DIFFERENTIATION RATES ACCORDING TO AGE AND SEX OFDONORS, SITE OF MUSCLE BIOPSY, AND DELAY BEFORE PROCESSING, Biology of the cell, 89(3), 1997, pp. 233-240
Citations number
36
Categorie Soggetti
Cell Biology
Journal title
ISSN journal
02484900
Volume
89
Issue
3
Year of publication
1997
Pages
233 - 240
Database
ISI
SICI code
0248-4900(1997)89:3<233:PHMSC->2.0.ZU;2-7
Abstract
The present study was performed to determine the influence on human sa tellite cell yield, proliferation, and differentiation rates of: 1) se x and age of donors; 2) site of the muscle biopsy; and 3) delay before processing of the muscle biopsy sample. We used a standardized primar y muscle cell culture procedure on 206 normal muscle samples obtained from different muscle groups of patients aged from 20 to 88 years, at time of orthopedic surgery. Sex of donors did not influence muscle cul ture parameters. In contrast, aging tended to affect muscle cell yield (age group 50-59 years vs 70-79 years, P < 0.08), but not myogenic ce ll abilities to proliferate and to fuse into myotubes. The anatomic or igin of muscle samples used for culture appeared to influence culture parameters. In contrast with other tested muscles, the tensor fasciae muscle gave both a good cell yield (174 +/- 25 10(3) cells per gram) a nd homogeneous proliferation and differentiation rates. Storage of the muscle sample at 4 degrees C in transport medium was associated with a very high cell yield when processing was done in early hours after b iopsy (277 +/- 50 10(3) cells/g), a high and stable cell yield when pr ocessing was done from day 1 to day 3 after biopsy (185 +/- 15 10(3) c ells/g), and a poor cell yield when processing was done after day 4 (1 11 +/- 13 10(3) cells/g). Storage of muscle biopsy samples at 4 degree s C for 1 to 4 days was associated with good proliferation and fusion rates. In conclusion, these data validate a convenient procedure of pr imary human muscle cell culture, using tensor fasciae muscle biopsy, w hich is easily done at time of orthopedic surgery, obtained from men a nd women of all ages (if possible less than 70 years to obtain good ce ll yield), and allowing of 1-3 days of storage before processing that may compensate uncertainty of the exact time of availability of muscle samples for the scientist.