Introduction: Macrophages reside within the interstitial compartment of the testis and form junction complexes with Leydig cells in vivo. We have previously shown that testicular macrophages produce a factor that stimulates testosterone secretion by Leydig cells while peritoneal macrophages have no effect. The purpose of the studies of this application is to investigate the development and regulation of this paracrine phenomenon. Hypothesis: Monocytes from bone marrow migrate to the testis at an important time of development and a subpopulation of these cells are then influenced by local testicular factors in interact with Leydig cells.
Specific Aims : 1. determine if the initial appearance of macrophages in the testis or the development of junctions between Leydig cells and macrophages occurs during an important time in testicular development, 2. determine if factors from the local testicular environment are involved in the differentiation or regulation of macrophages. Methods: We will determine the stage of development that macrophages first appear in the testis using light microscopic immunocytochemical methods. To determine when junctional complexes form between the macrophages and Leydig cells we will study the testes from animals at various stages of development or postnatal maturation using electron microscopic techniques. We will employ retrovirus mediated gene-transfer studies to determine if stem cells in the bone marrow produce testicular macrophages. To determine if local testicular factors are capable of regulating or inducing the testis- specific phenotype, we will treat macrophages from the testis, blood (monocytes), peritoneum, lung and ovary with factors form testicular extracts, interstitial fluid or culture medium of various testicular cell types and then assay for testis-specific functions. Significance: These studies will contribute to an understanding of the regulation and differentiation of the interaction between macrophages and Leydig cells. Since these multidisciplinary studies are broad-based and employ both in vivo and in vitro methods, important information concerning the physiological relevance of testicular macrophages will be gained.

Agency
National Institute of Health (NIH)
Institute
Eunice Kennedy Shriver National Institute of Child Health & Human Development (NICHD)
Type
Research Project (R01)
Project #
5R01HD026733-03
Application #
2200065
Study Section
Reproductive Biology Study Section (REB)
Project Start
1990-09-01
Project End
1995-08-31
Budget Start
1992-09-01
Budget End
1995-08-31
Support Year
3
Fiscal Year
1992
Total Cost
Indirect Cost
Name
Texas Tech University
Department
Biochemistry
Type
Schools of Medicine
DUNS #
609980727
City
Lubbock
State
TX
Country
United States
Zip Code
79430
Moore, C; Hutson, J C (1994) Physiological relevance of tumor necrosis factor in mediating macrophage-Leydig cell interactions. Endocrinology 134:63-9
Raburn, D J; Coquelin, A; Reinhart, A J et al. (1993) Regulation of the macrophage population in postnatal rat testis. J Reprod Immunol 24:139-51
Hutson, J C (1993) Secretion of tumor necrosis factor alpha by testicular macrophages. J Reprod Immunol 23:63-72
Hutson, J C (1992) Development of cytoplasmic digitations between Leydig cells and testicular macrophages of the rat. Cell Tissue Res 267:385-9
Straus, D C; Lonon, M K; Hutson, J C (1992) Inhibition of rat alveolar macrophage phagocytic function by a Pseudomonas cepacia lipase. J Med Microbiol 37:335-40
Raburn, D J; Coquelin, A; Hutson, J C (1991) Human chorionic gonadotropin increases the concentration of macrophages in neonatal rat testis. Biol Reprod 45:172-7