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Journal of Histochemistry and Cytochemistry, Vol. 48, 1545-1552, November 2000, Copyright © 2000, The Histochemical Society, Inc.


ARTICLE

Tissue Distribution of the Lipocalin Alpha-1 Microglobulin in the Developing Human Fetus

Lennart E. Lögdberga, Bo Åkerströmb, and Sunil Badvea
a Department of Pathology, Albert Einstein College of Medicine & Montefiore Medical Center, Bronx, New York
b Section for Molecular Signaling, Department of Cell and Molecular Biology, University of Lund, Lund, Sweden

Correspondence to: Lennart E. Lögdberg, Laboratory of Stem Cell Biology, Lindsay F. Kimball Research Inst., New York Blood Center, 310 East 67th Street, New York, NY 10021. E-mail: Logdberg@nybc.org or Lindalennart@msn.com

Alpha-1 microglobulin ({alpha}1m), a lipocalin, is an evolutionarily conserved immunomodulatory plasma protein. In all species studied, {alpha}1m is synthesized by hepatocytes and catabolized in the renal proximal tubular cells. {alpha}1m deficiency has not been reported in any species, suggesting that its absence is lethal and indicating an important physiological role for this protein To clarify its functional role, tissue distribution studies are crucial. Such studies in humans have been restricted largely to adult fresh/frozen tissue. Formalin-fixed, paraffin-embedded multi-organ block tissue from aborted fetuses (gestational age range 7–22 weeks) was immunohistochemically examined for {alpha}1m reactivity. Moderate to strong reactivity was seen at all ages in hepatocytes, renal proximal tubule cells, and a subset of pancreatic islet cells. Muscle (cardiac, skeletal, or smooth), adrenal cortex, a scattered subset of intestinal mucosal cells, tips of small intestinal villi, and Leydig cells showed weaker and/or variable levels of reactivity. Connective tissue stained with variable location and intensity. The following cells/sites were consistently negative: thymus, spleen, hematopoietic cells, lung parenchyma, glomeruli, exocrine pancreas, epidermis, cartilage/bone, ovary, seminiferous tubules, epididymis, thyroid, and parathyroid. The results underscore the dominant role of liver and kidney in fetal {alpha}1m metabolism and provide a framework for understanding the functional role of this immunoregulatory protein.

(J Histochem Cytochem 48:1545–1552, 2000)

Key Words: alpha-1-microglobulin, fetal, tissue distribution, lipocalin


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