Immunohistochemical demonstration of nerve growth factor receptor in bovine testis.

Cell Tissue Res

Institut für Anatomie der Universität, Universitätsstrasse 31, D-93040 Regensburg, Germany.

Published: August 1996

AI Article Synopsis

  • The study used an antibody to identify low-affinity nerve growth factor receptors in bovine testis tissue, showing strong expression in certain immature cells like fibroblast-like mesenchymal cells.
  • After these cells differentiated into Leydig and myoid cells, receptor expression decreased, while peritubular and intertubular fibroblasts continued to show positivity.
  • Additionally, the receptor was found in various stages of spermatogonia, with expression in A-spermatogonia and I-spermatogonia linked to the cell cycle, predominantly during the G1 phase, and was localized to the outer surface of those cells.

Article Abstract

Nerve growth factor receptor (low-affinity form) was demonstrated immunohistochemically in bovine testis by using a monoclonal mouse anti-human antibody. In the 7-month-old fetus and in the early postnatal testis, the peritubular and intertubular fibroblast-like mesenchymal cells showed a strong reaction. Following differentiation of these cells into Leydig and myoid peritubular cells, the nerve growth factor receptor was no longer expressed. However, peritubular and intertubular testicular fibroblasts/fibrocytes, which are also derived from mesenchymal precursors, remained positive. Additionally, the nerve growth factor receptor was demonstrated in postnatal prespermatogonia, A-spermatogonia, I-spermatogonia and members of the spermatogonia precursor cell line; B-spermatogonia remained negative. In A-spermatogonia and I-spermatogonia, the expression of the nerve growth factor receptor was cell-cycle-dependent and was mostly observed during G1-phase. Pre-embedding ultrahistochemistry with gold-conjugated antibody followed by silver-enhancement revealed that the nerve growth factor receptor was localized at the outer cell surface. The metal granules showed a regular distribution in positive spermatogonia. In testicular fibroblasts/fibrocytes the long narrow processes were preferentially decorated.

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http://dx.doi.org/10.1007/s004410050636DOI Listing

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