4.4 Article

Immunolabeling of gamma-glutamyl transferase 5 in normal human tissues reveals that expression and localization differ from gamma-glutamyl transferase 1

Journal

HISTOCHEMISTRY AND CELL BIOLOGY
Volume 143, Issue 5, Pages 505-515

Publisher

SPRINGER
DOI: 10.1007/s00418-014-1295-x

Keywords

Gamma-glutamyl transferase; Gamma-glutamyl transpeptidase; Leukotriene C-4; Glutathione; Glycoproteins

Funding

  1. Oklahoma Center for the Advancement of Science and Technology (OCAST) [HR11-085]
  2. National Institute of General Medical Sciences of the National Institutes of Health [P20GM103640]

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Gamma-glutamyl transferase (GGT5) was discovered due to its ability to convert leukotriene C-4 (LTC4, a glutathione S-conjugate) to LTD4 and may have an important role in the immune system. However, it was not known which cells express the enzyme in humans. We have developed a sensitive and specific antibody that can be used to detect human GGT5 on Western blots and in fixed tissue sections. We localized GGT5 expression in normal human tissues. We observed GGT5 expressed by macrophages present in many tissues, including tissue-fixed macrophages such as Kupffer cells in the liver and dust cells in the lung. GGT5 was expressed in some of the same tissues that have been shown to express gamma-glutamyl transferase (GGT1), the only other enzymatically active protein in this family. But, the two enzymes were often expressed by different cell types within the tissue. For example, GGT5 was expressed by the interstitial cells of the kidney, whereas GGT1 is expressed on the apical surface of the renal proximal tubules. Other tissues with GGT5-positive cells included: adrenal gland, salivary gland, pituitary, thymus, spleen, liver, bone marrow, small intestine, stomach, testis, prostate and placenta. GGT5 and GGT1 are cell surface enzymes. The different pattern of expression results in their access to different extracellular fluids and therefore different substrates. GGT5 has access to substrates in blood and intercellular fluids, while GGT1 has access primarily to fluids in ducts and glands throughout the body. These data provide new insights into the different functions of these two related enzymes.

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