 |
||||
| 2008 JASN IMPACT FACTOR 7.505 | HOME AUTHOR INFO EDITORIAL BOARD SUBSCRIBE FEEDBACK ALERTS HELP | |||
| CURRENT ISSUE | ARCHIVES | JASN Express | ONLINE SUBMISSION | |
|
||||
| 2008 JASN IMPACT FACTOR 7.505 | HOME AUTHOR INFO EDITORIAL BOARD SUBSCRIBE FEEDBACK ALERTS HELP | |||
| CURRENT ISSUE | ARCHIVES | JASN Express | ONLINE SUBMISSION | |
| ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Editorials |
Department of Anatomy and Cell Biology, University of Kansas Medical Center, Kansas City, Kansas
Address correspondence to: Dr. Dale R. Abrahamson, Department of Anatomy and Cell Biology, University of Kansas Medical Center, 3901 Rainbow Boulevard, MS 3038, Kansas City, KS 66160. Phone: 913-588-7000; Fax: 913-588-2710; E-mail: dabrahamson{at}kumc.edu
Therapeutic stem cell research is among the most exciting topics in biomedicine today. Many compelling studies have shown that mouse and human embryonic stem (ES) cells in culture are multipotent and can differentiate into a wide variety of cell types, depending on culture conditions (1). Applications of ES cells in vivo for tissue repair have also shown much therapeutic promise, although many theoretical and practical problems need to be overcome before this technology is fully robust. Nevertheless, several experiments in animals have shown that ES cells have the capacity for organotypic cell differentiation (2–4). For example, reasoning that the developing kidney microenvironment might provide appropriate cues for entry of ES cells into a nephrogenic program, we microinjected mouse ES cells that were tagged with a lineage marker into embryonic day 12 to 13 metanephroi (5). After 3 to 5 d in organ culture, ES cell derivatives predominantly differentiated into lumenized tubules with apical junctional complexes and primary cilia and assembled a basement membrane around their basal aspects. Many of these structures also expressed proximal tubule markers and Na+/K+ ATPase, all of which are signatures of a highly differentiated epithelium. Conversely, we found only rare evidence for integration of injected ES cells into the glomerular epithelial tufts that form in organ culture (5).
Owing in part to various difficulties with the few human ES cell lines that are available to most researchers in the United States and the ongoing debate regarding generating new lines of human ES cells, considerable efforts have been devoted to exploring adult somatic stem cells as alternatives, especially those derived from bone marrow (BMSC). These cells can be harvested not only from marrow chambers but also from umbilical cord or peripheral blood and therefore are readily available. Of course, grafting of autologous BMSC is a well-established procedure for restoring hematopoietic tissues in patients who have undergone intensive radiation and chemotherapies.
Beyond marrow reconstitution, there have been numerous reports during the past several years for the experimental repopulation of injured tissues by BMSC in diverse organs (cardiac muscle cells [6], central nervous system astrocytes and microglia [7], and hepatocytes [8]), including kidney. Similar to our findings with mouse ES cells, when human BMSC are injected into kidneys of intact mouse embryos during whole-embryo culture, BMSC differentiate into complex renal structures (9). Several studies showed recently that when BMSC are injected into mice that are undergoing experimental models of acute renal failure, stem cell derivatives are localized within the renal parenchyma, and, under certain conditions, they help to restore renal function (10–12). However, whether large numbers of extrinsic BMSC differentiate into functional renal cells in vivo was questioned recently. A careful study measured compartmentalization of systemically injected BMSC into mouse kidneys that were regenerating from postischemic injury (13). These experiments showed that BMSC derivatives accounted only for 11% of the proliferating epithelial cells of regenerating tubules, whereas 89% of reparative epithelial cells were derived from an intrinsic source. Moreover, >80% of the BMSC localized to the interstitium, where they appeared to be profibrotic and proinflammatory, actually worsening the recovery from acute renal failure (13).
Several obstacles confront potential therapies using extrinsic stem cells: Selection of appropriate cells, differentiation into harmful phenotypes, and delivery into discrete tissue compartments. Perhaps one reason that so many BMSC develop into interstitial cells rather than tubular epithelium in postischemic kidney is that this represents a default pathway adopted by the majority of these cells. Alternatively, the interstitium may represent a more permissive environment for BMSC survival/proliferation. One way to avert such difficulties may be to condition or otherwise manipulate stem cells before their delivery in vivo. In this issue of the JASN, canine BMSC were cultured on plastic, type I collagen matrices, or type IV collagen NC1 hexamers and compared with the behavior of an immortalized podocyte cell line (14). Like the cultured podocytes, BMSC expressed highest levels of 
1, 2, and 5 chains of type IV collagen and redistributed CD2AP into punctuate patterns only when cells were cultured on NC1 hexamer substrates. The authors conclude that culturing BMSC on type IV collagen substrates, which resembles matrix ordinarily seen by podocytes in vivo, promotes their partial differentiation in vitro into a podocyte-like phenotype (14). Whether these cultured cells could ever become functional podocytes in vivo is unknown, but this in vitro conditioning strategy with stem cells clearly underscores the importance of cell–matrix interrelationships in achieving appropriate phenotypes.
Another approach involves enrichment of certain stem cells from a larger, mixed pool. Considerable evidence has accumulated showing that BMSC and peripheral blood contain a relatively small number of endothelial progenitor cells (EPC) that express a restricted set of surface markers (CD31, CD34, and vascular endothelial growth factor receptor 2, among others) (15). Under certain conditions, these EPC-enriched fractions from blood exhibit properties that are similar to those of embryonic angioblasts and contribute to the endothelium of growing vessels and those that are undergoing repair. But these findings, too, are controversial. For example, others have shown that conditioned medium from BMSC/EPC and not the cells themselves are important for certain vascular therapies (16). Indeed, in mice with hind limb ischemia and reconstituted green fluorescent protein (GFP)-positive bone marrow, GFP cells did not co-localize with collateralizing endothelium or smooth muscle but instead accumulated as monocytes/macrophages in vascular peripheries. Nevertheless, these experiments have imposed some new thinking on roles for BMSC in vessel repair. Rather than direct incorporation of BMSC into endothelium, paracrine signals that are transmitted from stem cell derivatives seem to promote vascular growth (16).
The accessibility and microanatomy of certain target organs may present significant barriers to extrinsic stem cell therapy. This may be particularly true for the nephron, which contains dozens of morphologically and functionally distinct epithelial cells, all separated from the vasculature by continuous sheets of basement membrane. For stem cells that circulate in the blood to reach nephron epithelia directly (including glomerular podocytes), this basement membrane barrier would have to be breached, which may lead to a number of poor outcomes. Retrograde, ureteral administration of stem cells might result in repopulation of collecting duct or distal tubular epithelial cells but would require a long, tortuous journey to the proximal and glomerular compartments.
Problems of extrinsic cell access might be overcome through the stimulation of intrinsic stem cell beds, which of course exist in bone marrow, as we have been discussing, but also in other organs, including skin and gastrointestinal tract. A recent study reported that the adult renal papilla harbors an apparently large population of intrinsic stem cells (17). These cells were identified after the administration of bromodeoxyuridine in mice and shown to re-enter the cell cycle after ischemic injury. Whether these papillary cells specifically are the primary or sole source for cell renewal after renal injury remains to be proved. Nevertheless, these intriguing results are also consistent with evidence discussed earlier arguing for a primarily intrinsic, not extrinsic, origin of cells in regenerating kidney (13). Because these papillary stem cells are located in both tubular epithelial and interstitial compartments, therapeutic strategies that selectively stimulate either population may make basement membrane transgression unnecessary. Indeed, for kidney and other organ systems, technologies that target intrinsic stem cells may be our best bet for developing realistic, organotypic stem cell therapies in vivo.
Although intrinsic stem cells may ultimately prove to be an optimal target for regenerative medicine, in many cases, these cells are very poorly understood currently. Whether every organ system contains such populations is not known, and how to promote their differentiation selectively and otherwise manipulate them also are problematic. Therefore, much continued work on the biology of ES cells and BMSC are clearly needed to understand basic questions such as the composition and regulation of their respective niches and control of mobilization, proliferation, and differentiation of their derivatives. Among other approaches, continued experimentation with these cells through conditioning their microenvironment in vitro, such as the provision of various culture substrates as discussed by Perry et al. (14), should yield much valuable information on mechanisms that dictate stem cell fate. All of this information will be essential before the promises of stem cell research are fulfilled.
 |
Footnotes |
|---|
|
References |
|---|
 Top References |
|---|
Related Article
| ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
|
HOME
CURRENT ISSUE
ARCHIVES
JASN Express
ONLINE SUBMISSION
AUTHOR INFO
EDITORIAL BOARD SUBSCRIBE FEEDBACK ALERTS HELP |
