AI Article Synopsis

  • The study examined the expression, autophosphorylation, and localization of PKD2 in reactive lymph nodes and lymphoid tissue tumors, particularly non-Hodgkin's lymphoma (NHL) and Hodgkin's lymphoma (HL).
  • Specific antibodies were used to analyze tissue samples through immunohistochemical and biochemical methods, revealing PKD2 presence in tonsils and tumor tissues, while PKD1 was absent.
  • Findings indicated that PKD2 expression varies by type of lymphoma, being highest in activated B cell phenotypes and associated with higher levels of cell differentiation and activation.

Article Abstract

Aim: To study the PKD2 expression, autophosphorylation and localization in reactive lymph nodes and tumors of lymphoid tissues.

Materials And Methods: Specific antibodies, which recognize PKD1/2 or PKD2 and autophosphorylated PKD1/2, were used for immunohistochemical and biochemical studies of tonsils, reactive lymph nodes, tumor samples of non-Hodgkin's lymphoma (NHL) and Hodgkin's lymphoma (HL).

Results: Immunohistochemical and biochemical analysis of PKD1 and PKD2 expression showed PKD2 expression in tonsils, reactive lymph nodes and tumor tissues from patients with NHL and HL. Furthermore, we were not able to reveal PKD1 expression in studied lymphoid tissues. In tonsils and reactive lymph nodes the PKD2 expression was detected in T and B cell zones with highest level in germinal centers of lymphoid follicles and the maximum level of autophosphorylation in the light zones of the germinal centers. We found that low level of PKD2 expression and autophosphorylation was characteristic feature for mantle cell lymphomas, Burkitt's lymphomas, and in 50% of CLL/small lymphocytic lymphomas. Lymphoma cells of germinal center origin and with activated B cell phenotype (diffuse large B cell lymphomas, HL) and anaplastic large cells lymphoma demonstrated the high level of PKD2 expression and autophosphorylation.

Conclusions: The level of PKD2 expression and autophosphorylation in neoplastic cells corresponds to the expression pattern of this kinase in their normal analogs, and to the level of cell differentiation and activation.

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