| Citation | Zhu H, Li M, Zhao R, Li M, Chai Y, Zhu Z, Yang Y, Li W, Xie Z, Li X, Lei K, Li X, Ou G. The SPLiT-seq of late L3 larvae wild-type worms. Proc Natl Acad Sci U S A, 2022. |
| PubMed ID | 35666862 |
| Short Description | The SPLiT-seq of late L3 larvae wild-type worms. GEO Record: GSE167859, Platform: GPL25147 Lab Atlas: N.A. Other resources: N.A. |
| # of Conditions | 1 |
Full Description
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Microvilli are actin bundle-supported membrane protrusions essential for absorption, secretion, and sensation. Microvilli defects cause human diseases, including gastrointestinal disorders and inherited deafness; however, mechanisms controlling microvilli formation and organization remain unclear. Here, we study microvilli by vitrifying the C. elegans larvae and mouse intestinal tissues with high-pressure freezing, thinning them by cryo-focused ion beam milling, cryo-electron tomography, and sub-tomogram averaging. We show that hundreds of previously unrecognized stick-like structures, which we refer to as nanovilli, decorate the lateral surface of C. elegans and mouse microvilli. The C. elegans 37.5-nm long and 4.5-nm wide nanovilli are composed of the protocadherin family protein CDH-8. Loss of nanovilli slows down animal growth and increases the number of Y-shaped microvilli, intermediate structures when a microvillus splits from its tip and separates into two. Our results indicate that nanovilli space microvilli and suggest a microvilli division model through which microvilli assemble with striking uniformity. |
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