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29 May 2014 Age- and Species-Dependent Infiltration of Macrophages into the Testis of Rats and Mice Exposed to Mono-(2-Ethylhexyl) Phthalate (MEHP)
Caitlin J. Murphy, Angela R. Stermer, John H. Richburg
Author Affiliations +
Abstract

The mechanism by which noninfectious testicular inflammation results in infertility is poorly understood. Here the infiltration of CD11b immunoreactive testicular interstitial cells (neutrophil, macrophages, dendritic cells) in immature (Postnatal Day [PND] 21, 28, and 35) and adult (PND 56) Fischer rats is described at 12, 24, and 48 h after an oral dose of 1 g/kg mono-(2-ethylhexyl) phthalate (MEHP), a well-described Sertoli cell toxicant. Increases of CD11b cells are evident 12 h after MEHP exposure in PND 21 and 28 rats. In PND 28 rats, CD11b cells remained significantly elevated at 48 h, while in PND 21 rats, it returned to control levels by 24 h. The peak number of CD11b cells in PND 35 rat testis is delayed until 24 h, but remains significantly elevated at 48 h. In PND 56 rats, no increase in CD11b cells occurs after MEHP exposure. In PND 21, 28, and 35 rats, a significant increase in monocyte chemoattractant protein-1 (MCP-1) by peritubular myoid cells occurs 12 h after MEHP. Interestingly, MEHP treatment of C57BL/6J mice did not incite an infiltration of CD11b cells at either PND 21 or 28. The peak level of germ cell apoptosis observed 24 h after MEHP exposure in young rats is not seen in mice at any age or in PND 56 rats. Taken together, these findings implicate MCP-1 released by peritubular myoid cells in provoking the migration of CD11b cells into the immature rat testis early after MEHP exposure and point to a role for CD11b cells in triggering germ cell apoptosis in an age- and species-dependent manner.

Caitlin J. Murphy, Angela R. Stermer, and John H. Richburg "Age- and Species-Dependent Infiltration of Macrophages into the Testis of Rats and Mice Exposed to Mono-(2-Ethylhexyl) Phthalate (MEHP)," Biology of Reproduction 91(1), (29 May 2014). https://doi.org/10.1095/biolreprod.113.115527
Received: 1 November 2013; Accepted: 1 May 2014; Published: 29 May 2014
KEYWORDS
interstitial cells
macrophage
myoid cells
reproductive immunology
toxicology
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