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. 2022 Jan 19;322(3):C354–C369. doi: 10.1152/ajpcell.00411.2021

Table 2.

Cytokine quantification in MRcko mdx and WT skeletal muscle

TNF-α IL-1β M-CSF C5/C5a IL-4 IL-10 sICAM-1 TIMP-1 IL-1α IL-1ra
Coordinate D3 A10 C4 A2 B2 B6 A7 D2 A9 A11
MRcko
mdx 4WK QUAD +++ +++ ↑2.8× ↑1.2× +++ +++ ↓1% ↑1.2× +++ ↓6%
mdx 4WK DIA ↓20% ↓64% ↓10% ↓1% ↓45% ↓50% === === ↓50% ↓11%
 WT AID4 TA ↑1.6× N.D. ↑1.3× ↑1.1× N.D. N.D. === ↑1.1× N.D. ===

Quantification of relative cytokine levels detected in myeloid mineralocorticoid receptor knockout (MRcko) mdx and injured MRcko wild-type (WT) skeletal muscle by pixel densitometry. Results are displayed as fold increases and % decreases in MRcko skeletal muscle relative to the appropriate Cre controls. Coordinates listed in the table correspond to the individual chemokine’s location (in duplicate) on the immunoblot. Some quantified cytokines were equivalent (===) or not detected (N.D.) compared with Cre controls. Other cytokines were upregulated (+++) but, however, undetected in Cre controls and therefore excluded from quantification. AID4, 4 days after acute injury; DIA, diaphragm; M-CSF, macrophage colony-stimulating factor; QUAD, quadriceps; sICAM-1, soluble ICAM-1; TA, tibialis anterior; TIMP-1, tissue inhibitor of metalloproteinase-1; 4WK, 4 wk of age.