4.5 Article

CHHBP: a newly identified receptor of crustacean hyperglycemic hormone

Journal

JOURNAL OF EXPERIMENTAL BIOLOGY
Volume 219, Issue 8, Pages 1259-1268

Publisher

COMPANY OF BIOLOGISTS LTD
DOI: 10.1242/jeb.133181

Keywords

Glucose metabolism; Hormone receptor; Cell signaling; Protein-protein interaction; Cell surface receptor; Crustacean hyperglycemic hormone; Eriocheir sinensis

Categories

Funding

  1. National High Technology Research and Development Program of China [2012AA10A401]
  2. National Natural Science Foundation of China [31302168]
  3. Natural Science Foundation of Tianjin [14JCYBJC30700]
  4. Key Laboratory of freshwater aquaculture germplasm resources of Ministry of Agriculture: National Key Technology Program [2012BAD26B00]
  5. Science and PhD Start-up Fund of Tianjin Normal University [52XB1303]

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Crustacean hyperglycemic hormone (CHH) is a neurohormone found only in arthropods that plays a pivotal role in the regulation of hemolymph glucose levels, molting and stress responses. Although it was determined that a membrane guanylyl cyclase (GC) acts as the CHH receptor in the Y-organ during ecdysteroidogenesis, the identity of the CHH receptor in the hepatopancreas has not been established. In this study, we identified CHH binding protein (CHHBP), as a potential receptor by screening the annotated unigenes from the transcriptome of Eriocheir sinensis, after removal of the eyestalk. Analysis of the binding affinity between CHH and CHHBP provided direct evidence that CHH interacts with CHHBP in a specific binding mode. Subsequent analysis showed that CHHBP is expressed primarily in the hepatopancreas where it localizes to the cell membrane. In addition, real-time PCR analysis showed that CHHBP transcript levels gradually increase in the hepatopancreas following eyestalk ablation. RNA-imediated suppression of CHHBP expression resulted in decreased glucose levels. Furthermore, the reduction of blood glucose induced by CHHBP RNAi reached the same level as that observed in the eyestalk ablation group, suggesting that CHHBP is involved in glucose metabolism regulated by CHH. In addition, compared with the control group, injection of CHH was unable to rescue the decreased glucose levels in CHHBP RNAi crabs. CHH induced transport of 2-NBDG to the outside of cells, with indispensable assistance from CHHBP. Taken together, these findings suggest that CHHBP acts as one type of the primary signal processor of CHH-mediated regulation of cellular glucose metabolism.

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