G. Aust et al., EXPRESSION OF TUMOR-NECROSIS-FACTOR-ALPHA (TNF-ALPHA) MESSENGER-RNA AND PROTEIN IN PATHOLOGICAL THYROID-TISSUE AND CARCINOMA CELL-LINES, Clinical and experimental immunology, 105(1), 1996, pp. 148-154
There has been much controversy about the presence of TNF-alpha within
thyroid tissue. We therefore conducted a study to determine if TNF-al
pha mRNA is present in thyroid tissue and thyroid-derived cells. Semiq
uantitative reverse transcriptase-polymerase chain reaction (RT-PCR) w
as employed with a heterologous competitor fragment. Significantly low
er levels of TNF-alpha mRNA were found in the autonomous nodules from
patients with thyroid autonomy (TA, n = 4; 5.7 +/- 1.3 arbitrary units
(AU) (mean +/- s.e.m.); P < 0.03) and in normal thyroid tissue (n = 2
, 7.0 +/- 3.1 AU) compared with tissue from patients with Graves' dise
ase (GD; n = 13; 27.9 +/- 10.3 AU), non-toxic multinodular goitre (NTG
; n = 5; 20.9 +/- 5.8 AU) and perinodular tissue from TA patients (20.
3 +/- 4.0 AU). Higher levels were detected in tissues from patients wi
th Hashimoto's thyroiditis (HT; n = 2; 51.3 +/- 10.3 AU). Cultures of
pure thyroid-derived fibroblasts (46 +/- 18 AU), thyrocytes (33 +/- 8
AU), and the anaplastic thyroid carcinoma cell lines 8505 C (39 +/- 11
AU), SW 1736 (214 +/- 16 AU) and C 643 (3 +/- 1 AU) showed significan
tly lower TNF-alpha mRNA levels than thyroid-derived lymphocytes (1650
+/- 32 AU). TNF-alpha was detected in the supernatants of unstimulate
d lymphocytes (22.1 +/- 1.1 pg/ml) and SW 1736 cells (3.5 +/- 0.9 pg/m
l), but not in unstimulated fibroblasts and thyrocytes. Using an intra
cellular labelling technique in flow cytometry, the immunophenotype of
stimulated TNF-alpha-positive lymphocytes was determined as predomina
ntly CD3(+)CD45RO(+). Our results suggest that TNF-alpha is present in
the thyroid tissue of different thyroid disorders. Thyroid-derived ly
mphocytes are potential TNF-alpha producers and may thus locally influ
ence thyroid function.