The long-term goal of this project is to elucidate mechanisms underlying assembly of the enterocyte brush border: the sole site of nutrient absorption and the primary surface of interaction with bacteria and bacterial products that accumulate in the intestinal lumen. Found at the apex of the enterocyte, the brush border contains up to one thousand tightly packed, actin bundle-supported membrane protrusions known as microvilli, which extend off the cell surface to a nearly identical length. The functional consequence of this arrangement is an immense capacity for housing membrane-associated nutrient processing and host defense machinery that is required for maintaining gut homeostasis. Despite being positioned at a critical physiological interface in the GI tract, there s little information on how microvillar actin bundles are nucleated, how microvillar length is controlled, or how microvilli achieve perfectly tight packing during enterocyte differentiation. Using the CACO-2BBE cell culture model to explore the physical remodeling of the enterocyte apical surface during differentiation, our laboratory made a series of exciting discoveries that provide insight on fundamental mechanisms of brush border formation. During the early stages of brush border assembly, we observe that microvilli cluster together and interact at their tips to form 'tepee' shaped structures. As differentiation proceeds, the observed 'tepees' grow larger by incorporating more microvilli. Electron microscopy of these structures revealed, for the first time that adjacent microvilli in these tepees are physically connected to each other by thread-like links. These observations suggest that the tight packing of microvilli during brush border assembly may be driven by adhesion complexes that are inherent to these protrusions. We also identified a member of the cadherin superfamily, protocadherin-24 (PCDH24), which could play a role in forming inter-microvillar adhesion links. PCDH24 is a novel microvillar component that exhibits striking enrichment at microvillar tips (observed with super-resolution light microscopy and immuno- EM) and shRNA-mediated knockdown of this molecule significantly impairs microvillar packing during CACO- 2BBE differentiation. Based on these and other preliminary findings, we propose that PCDH24 creates inter- microvillar adhesion links at microvillar tips, which are required for the tight packing of these protrusions during brush border assembly.
The Aims proposed herein will begin to test this hypothesis by investigating: (1) the targeting and requirement for PCDH24 during brush border assembly and effacement by enteric pathogens, (2) the adhesion capacity of PCDH24, and (3) the mechanism underlying the microvillar tip localization of PCDH24. Given our expertise in defining the biological and physical underpinnings of brush border function, our group is well positioned to test this hypothesis and generate novel insight on this fundamental aspect of GI epithelial biology.
The epithelial cells that line the intestinal tract build hundreds of cylindrical protrusions on their apical surface; these 'microvilli' extend into the gut lumen, increasing the amount of apical membrane surface area available for nutrient absorption. Despite occupying a critical physiological interface in the gut, there is little information on how microvillar protrusions are built and/or maintained. The proposed work will elucidate molecular mechanisms underlying the construction of microvilli during the differentiation of intestinal epithelial cells and provide insight on the basis of human diseases characterized by loss of microvilli, which include enteric infections and inherited pathologies such as microvillus inclusio disease.
| Postema, Meagan M; Grega-Larson, Nathan E; Neininger, Abigail C et al. (2018) IRTKS (BAIAP2L1) Elongates Epithelial Microvilli Using EPS8-Dependent and Independent Mechanisms. Curr Biol 28:2876-2888.e4 |
| Tonucci, Facundo M; Ferretti, Anabela; Almada, Evangelina et al. (2018) Microtubules regulate brush border formation. J Cell Physiol 233:1468-1480 |
| Li, Jianchao; He, Yunyun; Weck, Meredith L et al. (2017) Structure of Myo7b/USH1C complex suggests a general PDZ domain binding mode by MyTH4-FERM myosins. Proc Natl Acad Sci U S A 114:E3776-E3785 |
| Kim, Sun Wook; Ehrman, Jonathan; Ahn, Mok-Ryeon et al. (2017) Shear stress induces noncanonical autophagy in intestinal epithelial monolayers. Mol Biol Cell 28:3043-3056 |
| Millis, Bryan A; Tyska, Matthew J (2017) High-Resolution Image Stitching as a Tool to Assess Tissue-Level Protein Distribution and Localization. Methods Mol Biol 1606:281-296 |
| McKinley, Eliot T; Sui, Yunxia; Al-Kofahi, Yousef et al. (2017) Optimized multiplex immunofluorescence single-cell analysis reveals tuft cell heterogeneity. JCI Insight 2: |
| Feng, Qiang; Bonder, Edward M; Engevik, Amy C et al. (2017) Disruption of Rab8a and Rab11a causes formation of basolateral microvilli in neonatal enteropathy. J Cell Sci 130:2491-2505 |
| Weck, Meredith L; Grega-Larson, Nathan E; Tyska, Matthew J (2017) MyTH4-FERM myosins in the assembly and maintenance of actin-based protrusions. Curr Opin Cell Biol 44:68-78 |
| Grega-Larson, Nathan E; Crawley, Scott W; Tyska, Matthew J (2016) Impact of cordon-bleu expression on actin cytoskeleton architecture and dynamics. Cytoskeleton (Hoboken) 73:670-679 |
| Taneja, Nilay; Fenix, Aidan M; Rathbun, Lindsay et al. (2016) Focal adhesions control cleavage furrow shape and spindle tilt during mitosis. Sci Rep 6:29846 |
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