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Laminin isoforms in human extraocular muscles

Kjellgren, Daniel (författare)
Umeå universitet,Oftalmiatrik
Thornell, Lars-Eric (författare)
Umeå universitet,Högskolan i Gävle,Belastningsskadecentrum,Anatomi
Virtanen, Ismo (författare)
visa fler...
Pedrosa-Domellöf, Fatima (författare)
Umeå universitet,Högskolan i Gävle,Belastningsskadecentrum,Anatomi,Oftalmiatrik
visa färre...
 (creator_code:org_t)
Association for Research in Vision and Ophthalmology (ARVO), 2004
2004
Engelska.
Ingår i: Investigative Ophthalmology and Visual Science. - : Association for Research in Vision and Ophthalmology (ARVO). - 0146-0404 .- 1552-5783. ; 45:12, s. 4233-4239
  • Tidskriftsartikel (refereegranskat)
Abstract Ämnesord
Stäng  
  • PURPOSE: To determine the laminin isoform composition of the basement membranes (BMs) in the human extraocular muscles (EOMs) and relate it to the fact that EOMs are spared in laminin alpha2-chain-deficient congenital muscular dystrophy. METHODS: Samples from adult human EOMs and limb muscle were processed for immunocytochemistry, with monoclonal antibodies against laminin chains (Ln) alpha1 to -5, beta1 and -2, and gamma1. Neuromuscular junctions (NMJs) were identified with acetylcholinesterase reaction. The capillary density was measured in sections stained with anti-Lnalpha5. RESULTS: The extrasynaptic BM of the EOM muscle fibers contained Lnalpha2, -beta1, -beta2, and -gamma1, and, in contrast to limb muscle, it also contained Lnalpha4 and -alpha5, to some extent. The distinct laminin composition of the EOMs was confirmed by the presence of Lutheran protein, an alpha5-chain-specific receptor not found in limb muscle. At the NMJs, there was increased expression of Lnalpha4 and expression of Lnalpha2, -alpha5, -beta1, -beta2, and -gamma1 was also maintained. The capillary density was very high (1050 +/- 190 capillaries/mm(2)) in the EOMs and significantly (P < 0.05) higher in the orbital (1170 +/- 180 capillaries/mm(2)) than in the global (930 +/- 110 capillaries/mm(2)) layer. CONCLUSIONS: The human EOMs showed important differences in laminin isoform composition and capillary density when compared with human limb muscle and muscles of other species. The presence of additional laminin isoforms other than laminin-2 in the BM of the extrasynaptic sarcolemma could partly explain the sparing of the EOMs in Lnalpha2-deficient congenital muscular dystrophy.

Ämnesord

MEDICIN OCH HÄLSOVETENSKAP  -- Klinisk medicin -- Oftalmologi (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Clinical Medicine -- Ophthalmology (hsv//eng)

Nyckelord

Adolescent
Adult
Aged
Aged
80 and over
Basement Membrane metabolism
Capillaries anatomy & histology
Extremities
Histocytochemistry
Humans
Immunohistochemistry
Infant
Newborn
Laminin metabolism
Middle Aged
Muscle Fibers metabolism
Muscle
Skeletal blood supply metabolism
Oculomotor Muscles blood supply metabolism
Protein Isoforms metabolism
Receptors
Laminin metabolism
Sarcolemma metabolism
Tissue Distribution
MEDICINE

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