Review Article

Biological Functionalities of Transglutaminase 2 and the Possibility of Its Compensation by Other Members of the Transglutaminase Family

Table 1

Members of the transglutaminase (TGase) enzyme family, their nomenclature, tissue distribution, biological functions, and pathological involvement [4, 30].

TGaseNomenclatureTissue distribution, cellular and subcellular localization Biological functionsPathology

TG1Keratinocyte TG, particulate TG, TG1, and TGKSquamous epithelia, keratinocytes, cytosolic, membraneBarrier function in stratified squamous epithelia, cornified envelope formation in keratinocyte differentiation Lamellar ichthyosis [119]

TG2Liver TG, tissue TG, cytosolic TG, erythrocyte TG, Ghα, and endothelial TGUbiquitously distributed in many types of tissue, cell membrane, cytosol, nucleus, extracellular Apoptosis, cell survival signalling, cell differentiation, matrix stabilization, endocytosis, and so forth Autoimmune diseases, neurodegenerative diseases, malignancies, metabolic diseases, and so forth [78]

TG3Epidermal TG, callus TG, hair follicle TG, and bovine snout TGEpidermis, hair follicle, brain, cytosolicTerminal differentiation of keratinocytes, hair follicles Human epidermis diseases

TG4Prostate TG, TGp, androgen regulated major secretory protein, vesiculase, dorsal prostate protein 1 (DP1), and type 4 TGProstate gland, prostatic fluids, and seminal plasma, extracellularReproduction and fertility, especially in rodents where it is involved in semen coagulationNot known

TG5TGX, type 5 TG, and TG5Ubiquitously expressed but predominant in female reproductive tissues, skeletal muscle, and foetal tissues, foreskin keratinocytes, epithelial barrier lining, cytosolicEpidermal differentiationSecondarily involved in hyperkeratotic phenotype in ichthyosis and in psoriasis, overexpressed or absent in different areas of the Darier’s disease lesions [120]

TG6TGY, type 6 TG, and TG6, Testis, lungs, and brain, cellular localization is yet to be definedCentral nervous system development, motor function, and late stage cell envelope formation in the epidermis and the hair follicleSpinocerebellar ataxias [121, 122]; polyglutamine (polyQ) diseases [123]

TG7TGZ, type 7 TG, TG7, and transglutaminase 7Ubiquitously expressed, prominent in testis and lungs, cellular and subcellular localization are unknown Not known

FXIIIAFactor XIII A, fibrin stabilizing factor, fibrinoligase, plasma TG, and Laki-Lorand factor Chondrocytes platelets, placenta, astrocytes, macrophages, synovial fluid, heart, eye, bone, dendritic cells in the dermis Wound healing, blood clotting, and bone growthF13A1 deficiency characterized by impaired wound healing, spontaneous abortion in women, subcutaneous and intramuscular haematomas, and severe bleeding tendency

Band 4.2Erythrocyte membrane protein band 4.2, B4.2, ATP-binding erythrocyte membrane protein band 4.2Surface of erythrocyte membranes, bone marrow, foetal liver, spleen, membranal Key component of erythrocyte skeletal network maintains erythrocyte shape and mechanical propertiesSpherocytic elliptocytosis