Season Dependent Changes in the Expression of Protein Kinase C Isoenzymes in a Female Patient with Systemic Lupus Erythematosus

The 20-year-old girl arrived in July (summer I) with some purpuras on the leg, maculopapular rash and livedo reticularis, oedema around the eyes and Raynaud’s phenomenon. White blood cell count was 3530 cells/mm³, platelet count was 79,000 cells/mm³. The autoantibody profile showed anti-nuclear antibody (ANA) positivity in 1:160 serum dilution (homogenous pattern), and an increased level of anti-dsDNA antibodies (74.1 versus 18 IU/ml). In addition, anti-platelet antibody positivity, lower complement factor 4 level (0.09 g/l), and anti-Epstein-Barr virus serum IgG positivity were demonstrated. Liver and renal tests were normal without proteinuria. The SLE was diagnosed according to the criteria of SLICC group based on the presence of photosensitivity, maculopapular rash, leukopenia, thrombocytopenia, ANA, anti-dsDNA positivity, representing an SLE Disease Activity Index (SLEDAI) value of 14. The therapy started with 0.5 mg/kg of methylprednisolone (MP) (32 mg in total) and 250 mg of hydroxychloroquine (HC). The dose of MD was gradually reduced to 8 mg until September, however the 250 mg of HC was continued.

The patient’s family history was negative for any autoimmune diseases; the 40-year-old healthy mother was still before menopause and working as hairdresser. The healthy 41-year-old father only with an abnormal glucose tolerance was working as truck driver. The 8-year-old younger brother was also healthy. The family belongs to the European white population.

In September, at the second visit of patient taking MP and HC, the clinical state improved remarkably (SLEDAI was 5) but the platelet cell count was still low (20,000 cells/mm³) without any bleeding complications. Therefore, the dose of MP was increased, HC remained and additionally azathioprine (AZA) was introduced (48 mg of MP + 250 mg of HC + 150 mg of AZA). In December (in winter), at the third visit, the dose of MP was reduced to 8 mg, HC and AZA therapies were continued. The platelet count was already elevated (112,000 cells/mm³) and SLEDAI was 8. In July, at the fourth visit (in summer II), the clinical state improved further (SLEDAI was 3), the platelet count became 196,000 cells/mm³ and 8 mg of MP was continued together with 250 mg of HC, while AZA treatment was stopped. The laboratory tests still showed ANA and anti-dsDNA positivity (60.9 IU/ml). Now, the patient has no clinical symptoms and receives 8 mg MP and 250 mg HC as maintenance therapy.

In December and the following July (summer II), the serum levels of three thyroid hormones free thyroxine (FT4), free triiodine-thyronine (FT3) and thyroid stimulating hormone (TSH) were measured in the patient.

All three members of family gave a written consent confirming their readiness to take part in this study and permit to publish the results.

We enrolled 6 women (range of age: 21–43 years) and 2 men (22 and 42 years old) who were chosen actually at the various visit times of patient and mother.

PBMC were isolated by Ficoll (Sigma-Aldrich, USA) gradient centrifugation. The expression of PKC isoenzymes were evaluated using western blotting and densitometry. Human β-actin served as an endogenous internal control.

Figure 1a demonstrates that at the first visit of the whole family in July (summer I), the expression of all PKC isoforms (α, β, δ, ε, η, θ) in the PBMC of healthy father was equally strong, and did not differ from the intensity of β-actin. On the other hand, the expression of isoenzymes was decreased remarkably both in the lupus patient and her healthy mother compared to the values of β-actin and the father’s results. For September, the intensive MP therapy elevated and almost restored the PKC levels, and resulted in a great improvement in the clinical state of patient.

However, in December (winter), both in the patient (treated with MP, HC and AZA) and her “SLE-free” healthy mother without any medication, the expression of the PKC isoenzymes elevated remarkably compared to the values of “female control 1” (28-year-old European white woman) (Fig. 1b).

Whereas in the following summer (summer II), the PKC values of both the patient (taking MP, HC and AZA) and her mother were lower again than those of “female control 4” (22-year-old European white woman) and “female control 5” (41-year-old European white woman) (Fig. 1c).

Table 1 presents all the numeric data of densitometry on the expression of PKC isoenzymes in PBMC of the family followed up for one year. In the data of the first visit in July (summer I), then in September, the values of father’s densitometry were regarded as 1.0 and the data of “mother” and “patient” were compared to them and to their internal control, β-actin. Later, in the further simultaneous studies on the cells of “mother” and “patient”, the data of densitometry were statistically compared to the average of 8 subjects forming the “group of healthy controls”. It was a striking surprise at the first visit that in the PBMC of healthy mother, the expression of each PKC isoenzymes showed not only significantly lower values than those in the healthy father and healthy controls (0.09 + 0.23 versus 1.04 + 0.24; p < 0.05), but they were even lower than those in her sick daughter (0.09 + 0.23 versus 0.33 + 0.27). In the patient, we recognized a similar pattern what we published earlier [1] showing significant decrease in the expression of various PKC isoenzymes (0.33 + 0.27 versus 1.04 + 0.27; p < 0.05), and the significant, almost total restoring effect of MP (0.88 + 0.64 versus 0.33 + 0.27 p < 0.05). However, at the following visit in December (winter), each PKC level, both in the mother and patient, increased significantly compared to the values of healthy controls (mother: 1.53 + 0.69; patient: 1.48 + 0.88; versus controls: 1.04 + 0.27; p < 0.05). On the other hand, in the following July (summer II), the PKC levels were significantly decreased again in both subjects, in the mother: 0.43 + 0.36; in the patient (taking 8 mg of GCS + HC): 0.58 + 0.48 versus in the controls: 1.04 + 0.27 (p < 0.05).

In Table 2, we summarized the changes in SLEDAI values of patient and doses of MP with other immunosuppressive drugs. Moreover, we also compared the serum levels of three thyroid hormones in December and following July. The three hormones, TSH, FT4 and FT3 regulating the seasonal adaptation, showed slightly higher concentrations in winter than in summer suggesting a moderate suppression of gonadotropin secretion. However, in summer the situation was inversed, the decreased thyroid hormone levels might involve an elevated gonadotropin secretion [2].