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Published on: March 26, 2015
Postnatal development of myosin heavy chain isoforms in rat extraocular muscles
Sang Jin Lim1, Hak Hyun Jung, Yoonae A Cho
1Department of Ophthalmology, Korea University College of Medicine, Sungbuk-Ku, Seoul, Republic of Korea.
Insights
Rat extraocular muscles (EOMs) show a developmental shift in myosin heavy chain (MHC) isoforms, transitioning from neonatal MHC to fast MHC types after birth, with distinct adult EOM compositions.
Area of Science:
- Muscle physiology
- Developmental biology
- Molecular biology
Background:
- Extraocular muscles (EOMs) have unique functional demands.
- Myosin heavy chain (MHC) isoforms determine muscle fiber type and contractile properties.
- Understanding MHC isoform development in EOMs is crucial for comprehending muscle adaptation.
Purpose of the Study:
- To investigate the myosin heavy chain (MHC) isoform composition in rat extraocular muscles (EOMs) during postnatal development.
- To analyze changes in MHC expression from birth to adulthood.
Main Methods:
- Competitive polymerase chain reaction (PCR) was used to quantify MHC mRNA levels.
- MHC composition was analyzed at postnatal day 0 (P0), postnatal day 14 (P14), and in adult rats.
- Specific analysis of MHC isoforms in each of the six adult EOMs was performed.
Main Results:
- At P0, neonatal MHC predominated (75.5%), with smaller amounts of embryonic MHC and 2A MHC.
- By P14, 2X MHC (42.4%) and 2A MHC (27.4%) became dominant, while neonatal and embryonic MHC decreased.
- Adult EOMs primarily expressed fast MHC isoforms (2X, 2A, 2B), with variations among the six EOMs.
Conclusions:
- A strong correlation exists between fast MHC isoform composition and muscle development.
- MHC isoform expression follows a neonatal-2X-2B pattern post-birth in EOMs.
- Postnatal EOM development exhibits unique MHC expression patterns potentially linked to functional requirements.
Purpose:
To determine the composition of myosin heavy chain (MHC) isoforms in rat extraocular muscles (EOMs) during postnatal development.
Methods:
The MHC composition of rat EOMs at postnatal day 0 (P0), postnatal day 14 (P14), and adults was evaluated at mRNA levels by competitive polymerase chain reaction and MHC composition of each six EOM in adult rats.
Results:
EOMs at P0 revealed predominant expression of neonatal MHC (75.5%) with a lesser percentage of embryonic MHC (12.8%) and 2A MHC (11.5%). 2X MHC was expressed at low levels and other MHC isoforms were not detected. At P14, EOMs expressed mostly 2X MHC (42.4%) and 2A MHC (27.4%). Expression levels of neonatal MHC (14.1%) and embryonic MHC (4.9%) decreased. 2B MHC (8.2%), EOM MHC (1.9%), and beta-cardiac MHC (1.1%) were detected at low levels. In the adult rats, EOMs contained over 80% of three fast MHC isoforms, such as 2X MHC (29.9%), 2A MHC (29.3%), and 2B MHC (24.5%). Each of six adult EOM showed slightly different expression levels of MHC composition.
Conclusions:
A strong correlation exists between the composition of fast MHC isoforms and muscle development. MHC isoform followed a neonatal MHC-2X MHC-2B MHC isoform switching pattern after birth. Postnatal development of EOMs had a slightly different expression pattern for MHC isoforms and may have different regulatory roles related to their functional requirement.
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