Review Volume 1, Issue 2 pp 157—181

Immune physiology in tissue regeneration and aging, tumor growth, and regenerative medicine

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Figure 3. Uterine ectocervix immunohistochemistry as indicated above columns. (A) Dendritic cell (DC) precursors secrete HLA-DR among parabasal cells (arrows) and differentiate into mature DC (arrowheads). (B) T cells migrate through parabasal layer (arrow) to parabasal/intermediate interface (dashed line) and show fragmentation after entering the intermediate layer (arrowheads). (C) Transformation of DC precursors into mature DC at the top of parabasal layer is associated with CD68 expression (arrow). Mature DC (black arrowheads) secrete CD68 material in intermediate layer accompanying mature (intermediate) and aged (superficial) epithelial cells (white arrowheads). (D) CD1a is expressed by DC precursors (arrows) and mature DC (black arrowheads). Mature DC (Langerhans' cells) undergo fragmentation in the mid intermediate layer (white arrowheads). (E) Strong IgM binding (arrowheads) in upper parabasal [1], upper intermediate [2] and upper superficial layers [3]. (F) IgG binds to the entire superficial layer. For abbreviations see Figure 2. Reprinted from Ref. [4], © Antonin Bukovsky.