Histochemistry and Cell Biology

, Volume 110, Issue 1, pp 33–41

Differential expression of moesin in cells of hematopoietic lineage and lymphatic systems

Authors

  • Junya Masumoto
    • Department of Molecular Oncology and Angiology, Research Center on Aging and Adaptation, Shinshu University School of Medicine, Asahi 3-1-1, Matsumoto 390, Nagano, Japan Tel. +81-263-37-2723; fax +81-263-37-2724
  • Junji Sagara
    • Department of Molecular Oncology and Angiology, Research Center on Aging and Adaptation, Shinshu University School of Medicine, Asahi 3-1-1, Matsumoto 390, Nagano, Japan Tel. +81-263-37-2723; fax +81-263-37-2724
  • Masayoshi Hayama
    • Department of Laboratory Medicine, Shinshu University School of Medicine, Asahi 3-1-1, Matsumoto 390, Nagano, Japan
  • Eiko Hidaka
    • Department of Laboratory Medicine, Shinshu University School of Medicine, Asahi 3-1-1, Matsumoto 390, Nagano, Japan
  • Tsutomu Katsuyama
    • Department of Laboratory Medicine, Shinshu University School of Medicine, Asahi 3-1-1, Matsumoto 390, Nagano, Japan
  • Shun’ichiro Taniguchi
    • Department of Molecular Oncology and Angiology, Research Center on Aging and Adaptation, Shinshu University School of Medicine, Asahi 3-1-1, Matsumoto 390, Nagano, Japan Tel. +81-263-37-2723; fax +81-263-37-2724
ORIGINAL PAPER

DOI: 10.1007/s004180050262

Cite this article as:
Masumoto, J., Sagara, J., Hayama, M. et al. Histochemistry (1998) 110: 33. doi:10.1007/s004180050262

Abstract

 Moesin is a member of the ERM family consisting of ezrin, radixin, and moesin. The protein is located in the plasma membrane similarly to ezrin and radixin, and is thought to regulate cellular movements and morphological changes. Using monoclonal antibody CR-22, the specificity of which against human moesin was confirmed by immunoprecipitation and western blotting analysis, we immunohistochemically stained various formalin-fixed and paraffin-embedded human tissues, in particular, clots of bone marrow and lymphatic tissues, to examine moesin expression in cells of hematopoietic lineage and lymphatic systems. In the bone marrow, moesin was expressed in myeloid cells, while little staining was detected in erythroid cells. Moesin was highly expressed in both the center and the periphery of mature megakaryocytes. In the lymphatic tissues, moesin was strongly expressed by T-lymphocytes in the paracortex. In the mantle zone, the periphery of the germinal center, moesin was expressed by small lymphocytes which were identified as B-lymphocytes. Furthermore, in areas of inflammation, moesin was expressed in both the center and the periphery of neutrophils, whereas in some neutrophils in distant areas, moesin was localized at the cellular periphery. These results suggest that differential expression of moesin in these cells is involved in their morphology and specialized functions.

Copyright information

© Springer-Verlag Berlin Heidelberg 1998