reproductive system
N |
• males exhibit no significant differences in testis weight or testis/body weight ratio relative to control males
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• only ~2% of epididymal sperm are motile but show a dramatic loss of progressive motility
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• only ~2% of epididymal sperm are motile but their motility, calculated as curvilinear velocity (VCL), is severely reduced
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• vast majority of epididymal sperm are immotile
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• testicular expression levels of IFT25 (the IFT27 binding partner) and IFT81 (a component of IFT-B complex) are significantly reduced
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• adult males show multiple signs of spermatogenesis failure during spermiogenesis
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• epididymal sperm count is severely reduced
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• sperm collected from the cauda epididymides show multiple abnormalities, including short, bent tails and round heads
• however, sperm lipid raft distribution appears to be normal
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• very few sperm appear to have a smooth tail; different light densities are observed along the whole tail
• most sperm have vesicles/vacuoles in some area along the flagella
• some epididymal sperm flagella have a distorted/damaged cell membrane
• however, branched sperm flagella are never observed
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• almost all epididymal sperm have misplaced or missing outer dense fibers (ODFs)
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• TEM analysis showed that almost all epididymal sperm show a disrupted 9 + 2 core axoneme structure and a disorganized axoneme microtubule array
• very few axoneme structures are detected in the seminiferous tubules
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• some sperm exhibit swollen tail tips
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• uneven thickness of sperm tails in some areas
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• TEM analysis of epididymal sperm showed that the mitochondria sheath is disorganized
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• TEM analysis of epididymal sperm showed that the fibrous sheath is disorganized
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• bent sperm tails are observed
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• round and other misshapen sperm heads are observed
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• round sperm heads are observed
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• very few developed sperm are found in the lumen of seminiferous tubules
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• cauda epididymis lumen is filled with abnormal sperm heads, cytoplasm bodies, sloughed round spermatids, sloughed aggregates of elongating spermatids, numerous detached sperm heads and abnormal short sperm tails that appear disorganized
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• when bred with adult wild-type females of known fertility, none of the 6-wk-old or adult males tested sired any pups/litters during a 2-month breeding period, indicating complete male sterility
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cellular
• epididymal sperm count is severely reduced
|
• sperm collected from the cauda epididymides show multiple abnormalities, including short, bent tails and round heads
• however, sperm lipid raft distribution appears to be normal
|
• very few sperm appear to have a smooth tail; different light densities are observed along the whole tail
• most sperm have vesicles/vacuoles in some area along the flagella
• some epididymal sperm flagella have a distorted/damaged cell membrane
• however, branched sperm flagella are never observed
|
• almost all epididymal sperm have misplaced or missing outer dense fibers (ODFs)
|
• TEM analysis showed that almost all epididymal sperm show a disrupted 9 + 2 core axoneme structure and a disorganized axoneme microtubule array
• very few axoneme structures are detected in the seminiferous tubules
|
• some sperm exhibit swollen tail tips
|
• uneven thickness of sperm tails in some areas
|
• TEM analysis of epididymal sperm showed that the mitochondria sheath is disorganized
|
• TEM analysis of epididymal sperm showed that the fibrous sheath is disorganized
|
• bent sperm tails are observed
|
• round and other misshapen sperm heads are observed
|
• round sperm heads are observed
|
• some epididymal sperm flagella have a distorted /damaged cell membrane
|
• only ~2% of epididymal sperm are motile but show a dramatic loss of progressive motility
|
• only ~2% of epididymal sperm are motile but their motility, calculated as curvilinear velocity (VCL), is severely reduced
|
• vast majority of epididymal sperm are immotile
|
endocrine/exocrine glands
• testicular expression levels of IFT25 (the IFT27 binding partner) and IFT81 (a component of IFT-B complex) are significantly reduced
|