Literature DB >> 9347793

Two Gq class G proteins are expressed in human keratinocytes.

B M Rock1, L Xin, J N Wilcox.   

Abstract

G proteins link many cell surface receptor generated signals to activation of multiple cellular processes in all tissues. There is specificity in the receptor interaction with the G protein and in the interaction of the specific G protein with different effector molecules. The purpose of this study was to determine some of the biologically relevant G proteins in keratinocytes. The G alpha subunit of the heterotrimeric G protein was investigated because much of the biologic activity and the receptor specificity resides there. A polymerase chain reaction strategy was used that amplified multiple G alpha gene segments between conserved primer sites from keratinocyte first strand cDNA. Two Gq class G proteins, G alpha 16 and G alpha y, were identified. Using northern analysis and in situ hybridization, mRNA of both of these genes were detected in keratinocytes in culture and in epidermal keratinocytes. G alpha y was expressed in multiple other cell types and tissues, but G alpha 16 was restricted in expression to keratinocytes and keratinocyte-derived adnexal structures in the skin. G alpha 16 has previously been reported to be limited in expression to hematopoietic cells. The physiologic receptor to which it couples in neutrophils is reported to be a C5a receptor. The receptor to which it couples in keratinocytes has not been elucidated but by analogy may be another chemokine receptor. We hypothesize that G alpha 16 is an important conduit for responses to inflammatory signals in keratinocytes.

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Year:  1997        PMID: 9347793     DOI: 10.1111/1523-1747.ep12337646

Source DB:  PubMed          Journal:  J Invest Dermatol        ISSN: 0022-202X            Impact factor:   8.551


  1 in total

1.  Signalling through the leukotriene B4 receptor involves both alphai and alpha16, but not alphaq or alpha11 G-protein subunits.

Authors:  R Gaudreau; C Le Gouill; S Métaoui; S Lemire; J Stankovà; M Rola-Pleszczynski
Journal:  Biochem J       Date:  1998-10-01       Impact factor: 3.857

  1 in total

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