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1.
Invest Ophthalmol Vis Sci ; 65(10): 17, 2024 Aug 01.
Article in English | MEDLINE | ID: mdl-39115865

ABSTRACT

Purpose: The Rho-associated protein kinase and myosin light chain kinase (ROCK/MYLK) pathway undeniably plays a pivotal role in the pathophysiology of primary open-angle glaucoma (POAG). In our study, we utilized both ocular hypertension (OHT) rabbit models and clinical investigations to gain invaluable insights that propel the development of novel treatments targeting proteins and genes associated with the trabecular meshwork (TM), thereby offering promising avenues for the management of POAG. Methods: Following microbead injections into the anterior chamber of the ocular cavity of rabbits, we observed elevated histiocyte numbers and immune scores for MYLK-4/ pMLC-2, alongside a reduction in the void space within the TM. Notably, treatment was performed with 0.1% ITRI-E-(S)-4046, a compound with dual kinase inhibitor (highly specific inhibitor of ROCK1/2 and MYLK4), significantly reduced intraocular pressure (IOP; P < 0.05) and expanded the void space within the TM (P < 0.0001) compared with OHT rabbits. In clinical investigations, we utilized whole transcriptome sequencing to analyze gene expression specifically related to the TM, obtained from patients (5 early-onset and 5 late-onset) undergoing trabeculectomy. Results: Our findings revealed 103 differential expression genes (DEGs) out of 265 molecules associated with the Rho family GTPase pathway, exhibiting a P value of 1.25E-10 and a z-score of -2.524. These results underscore significant differences between the early-onset and late-onset POAG and highlight the involvement of the ROCK/MYLK pathway. Conclusions: These findings underscore the critical involvement of the ROCK/MYLK pathway in both OHT-related and different onsets of POAG, providing valuable insights into the TM-related molecular mechanisms underlying the disease.


Subject(s)
Disease Models, Animal , Glaucoma, Open-Angle , Intraocular Pressure , Myosin-Light-Chain Kinase , Ocular Hypertension , Trabecular Meshwork , rho-Associated Kinases , Animals , Trabecular Meshwork/metabolism , Trabecular Meshwork/pathology , rho-Associated Kinases/genetics , Rabbits , Ocular Hypertension/genetics , Ocular Hypertension/physiopathology , Ocular Hypertension/metabolism , Intraocular Pressure/physiology , Humans , Glaucoma, Open-Angle/genetics , Glaucoma, Open-Angle/metabolism , Glaucoma, Open-Angle/physiopathology , Myosin-Light-Chain Kinase/genetics , Myosin-Light-Chain Kinase/metabolism , Male , Female , Signal Transduction , Aged , Middle Aged
2.
Gen Comp Endocrinol ; 351: 114482, 2024 05 15.
Article in English | MEDLINE | ID: mdl-38432348

ABSTRACT

In black porgy (Acanthopagrus schlegelii), the brain-pituitary-testis (Gnrh-Gths-Dmrt1) axis plays a vital role in male fate determination and maintenance, and then inhibiting female development in further (puberty). However, the feedback of gonadal hormones on regulating brain signaling remains unclear. In this study, we conducted short-term sex steroid treatment and surgery of gonadectomy to evaluate the feedback regulation between the gonads and the brain. The qPCR results show that male phase had the highest gths transcripts; treatment with estradiol-17ß (E2) or 17α-methyltestosterone (MT) resulted in the increased pituitary lhb transcripts. After surgery, apart from gnrh1, there is no difference in brain signaling genes between gonadectomy and sham fish. In the diencephalon/mesencephalon transcriptome, de novo assembly generated 283,528 unigenes; however, only 443 (0.16%) genes showed differentially expressed between sham and gonadectomy fish. In the present study, we found that exogenous sex steroids affect the gths transcription; this feedback control is related to the gonadal stage. Furthermore, gonadectomy may not affect gene expression of brain signaling (Gnrh-Gths axis). Our results support the communication between ovotestis and brain signaling (Gnrh-Gths-testicular Dmrt1) for the male fate.


Subject(s)
Perciformes , Sex Determination Processes , Animals , Female , Male , Sexual Maturation , Gonads/metabolism , Perciformes/metabolism , Gonadotropin-Releasing Hormone/genetics , Gonadotropin-Releasing Hormone/metabolism , Estradiol/pharmacology , Estradiol/metabolism , Fishes/metabolism , Gonadal Steroid Hormones/metabolism , Brain/metabolism , Gene Expression
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