Original Paper

Journal of Comparative Physiology B

, Volume 180, Issue 8, pp 1257-1265

First online:

Glycerol uptake by erythrocytes from warm- and cold-acclimated Cope’s gray treefrogs

  • David L. GoldsteinAffiliated withDepartment of Biological Sciences, Wright State University Email author 
  • , James FrisbieAffiliated withDepartment of Biological Sciences, Wright State University
  • , Andrew DillerAffiliated withDepartment of Biological Sciences, Wright State University
  • , Ram Naresh PandeyAffiliated withDepartment of Biological Sciences, Wright State University
  • , Carissa M. KraneAffiliated withDepartment of Biology, University of Dayton

Rent the article at a discount

Rent now

* Final gross prices may vary according to local VAT.

Get Access

Abstract

Cope’s gray treefrogs, Hyla chrysoscelis, accumulate glycerol during the period of cold acclimation that leads to the development of freeze tolerance. Glycerol must cross cell membranes in numerous processes during this time, including exit from hepatocytes where glycerol is synthesized and entry into other tissues, where glycerol is cryoprotective. Thus, we hypothesized that erythrocytes from H. chrysoscelis would be permeable to glycerol and that that permeability would be up-regulated during cold acclimation. Further, we hypothesized that glycerol permeability would be associated with the expression of aquaporins, particularly those from the glyceroporin sub-family. Erythrocytes from warm-acclimated treefrogs had high glycerol permeability at 20°C, as assessed by the time required for osmotic lysis following suspension in 0.2 M glycerol. That osmotic lysis, as well as uptake of radio-labeled glycerol, was inhibited by 0.3 mM HgCl3. Permeability assessed via osmotic lysis was markedly reduced at 5°C. These properties were similar in animals deriving from northern (Ohio) and southern (Alabama) populations, although suggestive (through statistical interactions) of greater glycerol permeability in northern animals. Erythrocytes expressed mRNA and protein for a previously described glyceroporin, HC-3. In cold-acclimated animals, HC-3 protein expression was up-regulated, but we could not detect a concomitant enhancement of glycerol permeability.

Keywords

Hyla chrysoscelis Cope’s gray treefrog Freeze tolerance Cryobiology Glycerol Erythrocyte Aquaporin Glyceroporin