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Expression of mitogen activated protein kinases in labial salivary glands of patients with Sjögren’s syndrome
  1. Hideki Nakamura,
  2. Atsushi Kawakami,
  3. Satoshi Yamasaki,
  4. Yojiro Kawabe,
  5. Tatsufumi Nakamura,
  6. Katsumi Eguchi
  1. First Department of Internal Medicine, Nagasaki University School of Medicine, Nagasaki, Japan
  1. Professor K Eguchi, First Department of Internal Medicine, Nagasaki University School of Medicine, 1–7–1 Sakamoto, Nagasaki City, Nagasaki 852–8501, Japan.

Abstract

OBJECTIVE The expression of CD40 and CD40 ligand (CD40L) in mononuclear cells (MNCs) infiltrating the salivary glands of patients with Sjögren’s syndrome (SS) has recently been reported. This study determined the expression of mitogen activated protein kinase (MAP kinase) superfamilies, which act as downstream effector molecules of CD40, in MNCs infiltrating labial salivary tissues in SS patients.

METHODS Six HTLV-I seronegative SS patients and 10 HTLV-I seropositive patients including five HTLV-I associated myelopathy (HAM) patients were examined. The expression of MAP kinase superfamilies in labial salivary glands was examined by immunohistochemistry containing the mirror section technique.

RESULTS Both active forms of c-Jun N-terminal kinase (JNK) and p38 were found in salivary infiltrating MNCs of SS patients. Only minimal expression of the active form of extracellular signal regulated kinase (ERK) was observed in these tissues, however, co-expression of active JNK and active p38 was confirmed by the mirror section technique. Furthermore, these protein kinases were co-expressed in CD40+ MNCs. No difference in expression levels of active JNK and p38 was found in patients who were positive or negative for anti-HTLV-I antibody.

CONCLUSION These results indicate that JNK and p38, but not ERK, function as downstream effector molecules of CD40 in salivary infiltrating MNCs in SS patients, and suggest that these molecules may be involved in the pathological process of chronic sialadenitis in SS.

  • Sjögren’s syndrome
  • protein kinases
  • salivary glands

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