Jeffrey H. Miner, Ph.D.

Associate Professor
Department of Medicine

Renal Division
Department of Cell Biology and Physiology
Box 8126

tel: (314) 362-8235
fax: (314) 362-8237
email: minerj@wustl.edu
web: Personal Weblink

 

 

RESEARCH INTEREST

My research has two major focuses. The first deals with the roles of basement membranes, a specialized extracellular matrix, in embryonic development, organ function, and disease. Of particular interest are members of the laminin and collagen IV families and their roles in the kidney.
We have identified developmental transitions in laminin and collagen IV chain expression which parallel the stages of kidney development, and we have shown using knockout mice that these transitions are critical for maturation of the glomerular basement membrane, a component of the kidney's filtration apparatus. In addition, laminin alpha5 knockout mice exhibit a range of embryonic developmental defects that impair neural tube closure, limb patterning, placentation, and kidney and lung development. This underscores the importance of basement membranes in a variety of developmental processes. We are currently studying conditional laminin alpha5 knockout mice in order to better understand its role in mature kidney, lung, muscle, and intestine.
My second major interest concerns the role of fatty acid transport protein 4 (FATP4) in skin and hair development and in dietary fatty acid uptake. We discovered through positional cloning that mutation of FATP4 results in "wrinkle free" mice. These mice have very tight, thick skin and die shortly after birth because they are unable to breathe properly. In addition, grafted skin from the mutant exhibits impaired hair growth. We are now using biochemical, cell biological, and genetic techniques to determine the mechanism whereby FATP4 activity leads to normal skin development and normal hair growth. We are also investigating whether mice lacking FATP4 in the intestine have impaired dietary fat uptake.

SELECTED PUBLICATIONS

Moulson CL, Go G, Gardner JM, van der Wal A, Sillevis Smitt JH, van Hagen JM, and Miner JH. Homozygous and compound heterozygous mutations in ZMPSTE24 cause the laminopathy restrictive dermopathy. J. Invest. Dermatol. 2005. In Press.

Nguyen NM, Kelley DG, Schlueter JA, Meyer MJ, Senior RM, Miner JH. Epithelial laminin _5 is necessary for distal epithelial cell maturation, VEGF production, and alveolization in the developing murine lung. Dev Biol 2005 282:111-125.

Miner JH, Li C, Mudd JL, Go G, Sutherland AE. Compositional and structural requirements for laminin and basement membranes during mouse embryo implantation and gastrulation. Development 2004 131: 2247-2256.

Moulson CL, Martin DR, Lugus JJ, Schaffer JE, Lind AC, Miner JH. Cloning of wrinkle free, a previously uncharacterized mouse mutation, reveals crucial roles for fatty acid transport protein 4 in skin and hair development. Proc Natl Acad Sci USA 2003 100: 5274-5279.